| Year |
Citation |
Score |
| 2023 |
Thomas RM, Obbard DB, Lipshutz BH. Challenging cross couplings, in water, aided by iodination of (hetero)aromatic bromides. Chemical Science. 14: 13503-13507. PMID 38033910 DOI: 10.1039/d3sc04199a |
0.367 |
|
| 2023 |
Kincaid JRA, Wong MJ, Akporji N, Gallou F, Fialho DM, Lipshutz BH. Introducing Savie: A Biodegradable Surfactant Enabling Chemo- and Biocatalysis and Related Reactions in Recyclable Water. Journal of the American Chemical Society. PMID 36753354 DOI: 10.1021/jacs.2c13444 |
0.812 |
|
| 2021 |
Singhania V, Cortes-Clerget M, Dussart-Gautheret J, Akkachairin B, Yu J, Akporji N, Gallou F, Lipshutz BH. Lipase-catalyzed esterification in water enabled by nanomicelles. Applications to 1-pot multi-step sequences. Chemical Science. 13: 1440-1445. PMID 35222928 DOI: 10.1039/d1sc05660c |
0.805 |
|
| 2021 |
Akporji N, Singhania V, Dussart-Gautheret J, Gallou F, Lipshutz BH. Nanomicelle-enhanced, asymmetric ERED-catalyzed reductions of activated olefins. Applications to 1-pot chemo- and bio-catalysis sequences in water. Chemical Communications (Cambridge, England). 57: 11847-11850. PMID 34698744 DOI: 10.1039/d1cc04774d |
0.811 |
|
| 2020 |
Akporji N, Thakore RR, Cortes-Clerget M, Andersen J, Landstrom E, Aue DH, Gallou F, Lipshutz BH. NPhos - an easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki-Miyaura cross couplings in water. Chemical Science. 11: 5205-5212. PMID 34122976 DOI: 10.1039/d0sc00968g |
0.819 |
|
| 2020 |
Lipshutz BH, Takale BS, Thakore RR, Casotti G, Li X, Gallou F. Mild and robust Stille reactions in water using ppm levels of a new triphenylphosphine-based palladacycle. Angewandte Chemie (International Ed. in English). PMID 33180988 DOI: 10.1002/anie.202014141 |
0.364 |
|
| 2020 |
Lipshutz BH, Yu TY, Pang H, Cao Y, Gallou F. Safe, Scalable, Inexpensive, and Mild Nickel-Catalyzed Migita-like C-S Cross-Couplings in Recyclable Water. Angewandte Chemie (International Ed. in English). PMID 33095957 DOI: 10.1002/anie.202013017 |
0.373 |
|
| 2020 |
Thakore RR, Takale BS, Casotti G, Gao ES, Jin HS, Lipshutz BH. Chemoselective Reductive Aminations in Aqueous Nanoreactors Using Parts per Million Level Pd/C Catalysis. Organic Letters. PMID 32806206 DOI: 10.1021/Acs.Orglett.0C02156 |
0.427 |
|
| 2020 |
Landstrom EB, Akporji N, Lee NR, Gabriel CM, Braga FC, Lipshutz BH. One-Pot Synthesis of Indoles and Pyrazoles via Pd-Catalyzed Couplings/Cyclizations Enabled by Aqueous Micellar Catalysis. Organic Letters. 22: 6543-6546. PMID 32806139 DOI: 10.1021/Acs.Orglett.0C02315 |
0.83 |
|
| 2020 |
Lipshutz BH, Wood AB, Cortes-Clerget M, Kincaid JA, Akkachairin B, Singhania V, Gallou F. Nickel Nanoparticle-Catalyzed Mono- and Di-Reductions of <i>gem</i>-Dibromocyclopropanes Under Mild, Aqueous Micellar Conditions. Angewandte Chemie (International Ed. in English). PMID 32579762 DOI: 10.1002/Anie.202006162 |
0.431 |
|
| 2020 |
Lee NR, Moghadam FA, Braga FC, Lippincott DJ, Zhu B, Gallou F, Lipshutz BH. Sustainable Palladium-Catalyzed Tsuji-Trost Reactions Enabled by Aqueous Micellar Catalysis. Organic Letters. PMID 32551706 DOI: 10.1021/Acs.Orglett.0C01329 |
0.459 |
|
| 2020 |
Takale BS, Thakore RR, Irvine NM, Schuitman AD, Li X, Lipshutz BH. Sustainable and Cost-Effective Suzuki-Miyaura Couplings toward the Key Biaryl Subunits of Arylex and Rinskor Active. Organic Letters. PMID 32521158 DOI: 10.1021/Acs.Orglett.0C01625 |
0.44 |
|
| 2020 |
Takale BS, Thakore RR, Etemadi-Davan E, Lipshutz BH. Recent advances in Cu-catalyzed C(sp)-Si and C(sp)-B bond formation. Beilstein Journal of Organic Chemistry. 16: 691-737. PMID 32362947 DOI: 10.3762/Bjoc.16.67 |
0.374 |
|
| 2020 |
Akporji N, Thakore RR, Cortes-Clerget M, Andersen J, Landstrom E, Aue DH, Gallou F, Lipshutz BH. N2Phos. An easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki-Miyaura cross couplings in water Chemical Science. 11: 5205-5212. DOI: 10.1039/D0Sc00968G |
0.831 |
|
| 2020 |
Takale BS, Thakore RR, Gao ES, Gallou F, Lipshutz BH. Environmentally responsible, safe, and chemoselective catalytic hydrogenation of olefins: ppm level Pd catalysis in recyclable water at room temperature Green Chemistry. DOI: 10.1039/D0Gc02087G |
0.402 |
|
| 2020 |
Wood AB, Nandiwale KY, Mo Y, Jin B, Pomberger A, Schultz VL, Gallou F, Jensen KF, Lipshutz BH. Continuous flow Suzuki–Miyaura couplings in water under micellar conditions in a CSTR cascade catalyzed by Fe/ppm Pd nanoparticles Green Chemistry. 22: 3441-3444. DOI: 10.1039/D0Gc00378F |
0.326 |
|
| 2020 |
Takale BS, Thakore RR, Mallarapu R, Gallou F, Lipshutz BH. A Sustainable 1-Pot, 3-Step Synthesis of Boscalid Using Part per Million Level Pd Catalysis in Water Organic Process Research & Development. 24: 101-105. DOI: 10.1021/Acs.Oprd.9B00455 |
0.342 |
|
| 2019 |
Zhang Y, Takale BS, Gallou F, Reilly J, Lipshutz BH. Sustainable ppm level palladium-catalyzed aminations in nanoreactors under mild, aqueous conditions. Chemical Science. 10: 10556-10561. PMID 32110341 DOI: 10.1039/C9Sc03710A |
0.402 |
|
| 2019 |
Takale BS, Thakore RR, Handa S, Gallou F, Reilly J, Lipshutz BH. A new, palladacycle for ppm level Pd-catalyzed Suzuki-Miyaura cross couplings in water. Chemical Science. 10: 8825-8831. PMID 31803456 DOI: 10.1039/C9Sc02528F |
0.436 |
|
| 2019 |
Pang H, Wang Y, Gallou F, Lipshutz BH. Fe-catalyzed reductive couplings of terminal (hetero)aryl alkenes and alkyl halides under aqueous micellar conditions. Journal of the American Chemical Society. PMID 31560526 DOI: 10.1021/Jacs.9B04510 |
0.406 |
|
| 2019 |
Lipshutz BH, Slack E, Seupel R, Aue D, Bringmann G. Atroposelective Total Synthesis of the Fourfold ortho-Substituted Naphthyltetrahydroisoquinoline Biaryl O,N-Dimethylhamatine. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31486170 DOI: 10.1002/Chem.201903832 |
0.368 |
|
| 2019 |
Gholinejad M, Oftadeh E, Shojafar M, Sansano JM, Lipshutz BH. Synergistic Effects of ppm Levels of Palladium on Natural Clinochlore for Reduction of Nitroarenes. Chemsuschem. 12: 4240-4248. PMID 31390483 DOI: 10.1002/Cssc.201901535 |
0.392 |
|
| 2019 |
Cortes-Clerget M, Akporji N, Zhou J, Gao F, Guo P, Parmentier M, Gallou F, Berthon JY, Lipshutz BH. Bridging the gap between transition metal- and bio-catalysis via aqueous micellar catalysis. Nature Communications. 10: 2169. PMID 31092815 DOI: 10.1038/S41467-019-09751-4 |
0.817 |
|
| 2019 |
Jin B, Gallou F, Reilly J, Lipshutz BH. ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors. Chemical Science. 10: 3481-3485. PMID 30996938 DOI: 10.1039/C8Sc05618H |
0.467 |
|
| 2019 |
Cortes-Clerget M, Lee NR, Lipshutz BH. Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions. Nature Protocols. PMID 30903108 DOI: 10.1038/S41596-019-0130-1 |
0.417 |
|
| 2019 |
Lee N, Cortes-Clerget M, Wood A, Lippincott D, Pang H, Moghadom F, Gallou F, Lipshutz BH. Coolade. A Low-Foaming Surfactant for Organic Synthesis in Water. Chemsuschem. PMID 30889298 DOI: 10.1002/Cssc.201900369 |
0.377 |
|
| 2019 |
Takale BS, Thakore RR, Kong FY, Lipshutz BH. An environmentally responsible 3-pot, 5-step synthesis of the antitumor agent sonidegib using ppm levels of Pd catalysis in water Green Chemistry. 21: 6258-6262. DOI: 10.1039/C9Gc03495A |
0.319 |
|
| 2019 |
Thakore RR, Takale BS, Gallou F, Reilly J, Lipshutz BH. N,C-Disubstituted Biarylpalladacycles as Precatalysts for ppm Pd-Catalyzed Cross Couplings in Water under Mild Conditions Acs Catalysis. 9: 11647-11657. DOI: 10.1021/Acscatal.9B04204 |
0.416 |
|
| 2019 |
Handa S, Jin B, Bora PP, Wang Y, Zhang X, Gallou F, Reilly J, Lipshutz BH. Sonogashira Couplings Catalyzed by Fe Nanoparticles Containing ppm Levels of Reusable Pd, under Mild Aqueous Micellar Conditions Acs Catalysis. 9: 2423-2431. DOI: 10.1021/Acscatal.9B00007 |
0.417 |
|
| 2019 |
Landstrom EB, Nichol M, Lipshutz BH, Gainer MJ. Discovery-Based SNAr Experiment in Water Using Micellar Catalysis Journal of Chemical Education. 96: 2668-2671. DOI: 10.1021/Acs.Jchemed.9B00310 |
0.373 |
|
| 2019 |
Akporji N, Lieberman J, Maser M, Yoshimura M, Boskovic Z, Lipshutz BH. Selective Deprotection of the Diphenylmethylsilyl (DPMS) Hydroxyl Protecting Group under Environmentally Responsible, Aqueous Conditions Chemcatchem. 11: 5743-5747. DOI: 10.1002/Cctc.201901232 |
0.784 |
|
| 2018 |
Lippincott DJ, Trejo-Soto PJ, Gallou F, Lipshutz BH. Copper-Catalyzed Oxidative Cleavage of Electron-Rich Olefins in Water at Room Temperature. Organic Letters. PMID 30102546 DOI: 10.1021/Acs.Orglett.8B01883 |
0.448 |
|
| 2018 |
Lippincott DJ, Linstadt RTH, Maser MR, Gallou F, Lipshutz BH. Synthesis of Functionalized 1,3-Butadienes via Pd-Catalyzed Cross-Couplings of Substituted Allenic Esters in Water at Room Temperature. Organic Letters. PMID 30080419 DOI: 10.1021/Acs.Orglett.8B01377 |
0.396 |
|
| 2018 |
Romney DK, Arnold FH, Lipshutz BH, Li CJ. Chemistry Takes a Bath: Reactions in Aqueous Media. The Journal of Organic Chemistry. 83: 7319-7322. PMID 30025465 DOI: 10.1021/Acs.Joc.8B01412 |
0.377 |
|
| 2018 |
Lee NR, Linstadt RTH, Gloisten DJ, Gallou F, Lipshutz BH. B-Alkyl sp-sp Suzuki-Miyaura Couplings under Mild Aqueous Micellar Conditions. Organic Letters. PMID 29738254 DOI: 10.1021/Acs.Orglett.8B00961 |
0.408 |
|
| 2018 |
Lipshutz BH, Ghorai S, Cortes-Clerget M. The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry "in Water". Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29465785 DOI: 10.1002/Chem.201705499 |
0.389 |
|
| 2018 |
Handa S, Smith JD, Zhang Y, Takale BS, Gallou F, Lipshutz BH. Sustainable HandaPhos-ppm Palladium Technology for Copper-Free Sonogashira Couplings in Water under Mild Conditions. Organic Letters. PMID 29341621 DOI: 10.1021/Acs.Orglett.7B03621 |
0.479 |
|
| 2018 |
Landstrom EB, Handa S, Aue DH, Gallou F, Lipshutz BH. EvanPhos: a ligand for ppm level Pd-catalyzed Suzuki–Miyaura couplings in either organic solvent or water Green Chemistry. 20: 3436-3443. DOI: 10.1039/C8Gc01356J |
0.459 |
|
| 2018 |
Pang H, Gallou F, Sohn H, Camacho-Bunquin J, Delferro M, Lipshutz BH. Synergistic effects in Fe nanoparticles doped with ppm levels of (Pd + Ni). A new catalyst for sustainable nitro group reductions Green Chemistry. 20: 130-135. DOI: 10.1039/C7Gc02991H |
0.312 |
|
| 2018 |
Lipshutz BH. Synthetic chemistry in a water world. New rules ripe for discovery Current Opinion in Green and Sustainable Chemistry. 11: 1-8. DOI: 10.1016/J.Cogsc.2017.10.004 |
0.352 |
|
| 2018 |
Lipshutz BH. Catalyst: Imagine Doing Chemistry at No Cost … to the Environment! Chem. 4: 2004-2007. DOI: 10.1016/J.Chempr.2018.08.031 |
0.343 |
|
| 2018 |
Lipshutz BH, Ghorai S, Cortes‐Clerget M. Frontispiece: The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry “in Water” Chemistry: a European Journal. 24. DOI: 10.1002/Chem.201882662 |
0.307 |
|
| 2017 |
Lee NR, Bikovtseva AA, Cortes-Clerget M, Gallou F, Lipshutz BH. Carbonyl Iron Powder: A Reagent for Nitro Group Reductions under Aqueous Micellar Catalysis Conditions. Organic Letters. 19: 6518-6521. PMID 29206473 DOI: 10.1021/Acs.Orglett.7B03216 |
0.336 |
|
| 2017 |
Klumphu P, Desfeux C, Zhang Y, Handa S, Gallou F, Lipshutz BH. Micellar catalysis-enabled sustainable ppm Au-catalyzed reactions in water at room temperature. Chemical Science. 8: 6354-6358. PMID 28989668 DOI: 10.1039/C7Sc02405C |
0.477 |
|
| 2017 |
Lipshutz BH. When Does Organic Chemistry Follow Nature's Lead and "Make the Switch"? The Journal of Organic Chemistry. 82: 2806-2816. PMID 28301935 DOI: 10.1021/Acs.Joc.7B00010 |
0.324 |
|
| 2017 |
Linstadt RT, Peterson CA, Jette CI, Boskovic ZV, Lipshutz BH. Control of Chemo-, Regio-, and Enantioselectivity in Copper Hydride Reductions of Morita-Baylis-Hillman Adducts. Organic Letters. PMID 28075138 DOI: 10.1021/Acs.Orglett.6B03464 |
0.724 |
|
| 2017 |
Lipshutz BH. The ‘Nano-to-Nano’ Effect Applied to Organic Synthesis in Water Johnson Matthey Technology Review. 61: 196-202. DOI: 10.1595/205651317X695785 |
0.302 |
|
| 2017 |
Cortes-Clerget M, Berthon J, Krolikiewicz-Renimel I, Chaisemartin L, Lipshutz BH. Tandem deprotection/coupling for peptide synthesis in water at room temperature Green Chemistry. 19: 4263-4267. DOI: 10.1039/C7Gc01575E |
0.332 |
|
| 2017 |
Adenot A, Landstrom EB, Gallou F, Lipshutz BH. Fe/ppm Cu nanoparticles as a recyclable catalyst for click reactions in water at room temperature Green Chemistry. 19: 2506-2509. DOI: 10.1039/C7Gc00883J |
0.381 |
|
| 2017 |
Isley NA, Wang Y, Gallou F, Handa S, Aue DH, Lipshutz BH. A Micellar Catalysis Strategy for Suzuki–Miyaura Cross-Couplings of 2-Pyridyl MIDA Boronates: No Copper, in Water, Very Mild Conditions Acs Catalysis. 7: 8331-8337. DOI: 10.1021/Acscatal.7B03241 |
0.452 |
|
| 2017 |
Gabriel CM, Parmentier M, Riegert C, Lanz M, Handa S, Lipshutz BH, Gallou F. Sustainable and Scalable Fe/ppm Pd Nanoparticle Nitro Group Reductions in Water at Room Temperature Organic Process Research & Development. 21: 247-252. DOI: 10.1021/Acs.Oprd.6B00410 |
0.345 |
|
| 2017 |
Lee NR, Gallou F, Lipshutz BH. SNAr Reactions in Aqueous Nanomicelles: From Milligrams to Grams with No Dipolar Aprotic Solvents Needed Organic Process Research & Development. 21: 218-221. DOI: 10.1021/Acs.Oprd.6B00388 |
0.351 |
|
| 2016 |
Gabriel CM, Lee NR, Bigorne F, Klumphu P, Parmentier M, Gallou F, Lipshutz BH. Effects of Co-solvents on Reactions Run under Micellar Catalysis Conditions. Organic Letters. PMID 27997200 DOI: 10.1021/Acs.Orglett.6B03468 |
0.395 |
|
| 2016 |
Lippincott DJ, Linstadt RT, Maser MR, Lipshutz BH. Synthesis of Functionalized [3], [4], [5] and [6]Dendralenes through Palladium-Catalyzed Cross-Couplings of Substituted Allenoates. Angewandte Chemie (International Ed. in English). PMID 27936307 DOI: 10.1002/Anie.201609636 |
0.472 |
|
| 2016 |
Nishikata T, Abela AR, Huang S, Lipshutz BH. Cationic Pd(II)-catalyzed C-H activation/cross-coupling reactions at room temperature: synthetic and mechanistic studies. Beilstein Journal of Organic Chemistry. 12: 1040-64. PMID 27340491 DOI: 10.3762/Bjoc.12.99 |
0.838 |
|
| 2016 |
Feng J, Handa S, Gallou F, Lipshutz BH. Safe and Selective Nitro Group Reductions Catalyzed by Sustainable and Recyclable Fe/ppm Pd Nanoparticles in Water at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 27305385 DOI: 10.1002/Anie.201604026 |
0.359 |
|
| 2016 |
Handa S, Andersson MP, Gallou F, Reilly J, Lipshutz BH. HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-catalyzed Cross-Couplings in Water at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 26924396 DOI: 10.1002/Anie.201510570 |
0.474 |
|
| 2016 |
Lipshutz BH, Gallou F, Handa S. Evolution of Solvents in Organic Chemistry Acs Sustainable Chemistry & Engineering. 4: 5838-5849. DOI: 10.1021/Acssuschemeng.6B01810 |
0.328 |
|
| 2016 |
Handa S, Smith JD, Hageman MS, Gonzalez M, Lipshutz BH. Synergistic and Selective Copper/ppm Pd-Catalyzed Suzuki–Miyaura Couplings: In Water, Mild Conditions, with Recycling Acs Catalysis. 6: 8179-8183. DOI: 10.1021/Acscatal.6B02809 |
0.473 |
|
| 2016 |
Handa S, Andersson MP, Gallou F, Reilly J, Lipshutz BH. Cover Picture: HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature (Angew. Chem. Int. Ed. 16/2016) Angewandte Chemie International Edition. 55: 4839-4839. DOI: 10.1002/Anie.201601719 |
0.414 |
|
| 2016 |
Handa S, Andersson MP, Gallou F, Reilly J, Lipshutz BH. Titelbild: HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature (Angew. Chem. 16/2016) Angewandte Chemie. 128: 4921-4921. DOI: 10.1002/Ange.201601719 |
0.416 |
|
| 2015 |
Isley NA, Linstadt RT, Kelly SM, Gallou F, Lipshutz BH. Nucleophilic Aromatic Substitution Reactions in Water Enabled by Micellar Catalysis. Organic Letters. 17: 4734-7. PMID 26368348 DOI: 10.1021/Acs.Orglett.5B02240 |
0.425 |
|
| 2015 |
Handa S, Wang Y, Gallou F, Lipshutz BH. Sustainable Fe-ppm Pd nanoparticle catalysis of Suzuki-Miyaura cross-couplings in water. Science (New York, N.Y.). 349: 1087-91. PMID 26339028 DOI: 10.1126/Science.Aac6936 |
0.427 |
|
| 2015 |
Handa S, Slack ED, Lipshutz BH. Nanonickel-Catalyzed Suzuki-Miyaura Cross-Couplings in Water. Angewandte Chemie (International Ed. in English). 54: 11994-8. PMID 26305994 DOI: 10.1002/Anie.201505136 |
0.433 |
|
| 2015 |
Fennewald JC, Landstrom EB, Lipshutz BH. Reductions of aryl bromides in water at room temperature. Tetrahedron Letters. 56: 3608-3611. PMID 26273116 DOI: 10.1016/J.Tetlet.2015.02.066 |
0.415 |
|
| 2015 |
Gabriel CM, Keener M, Gallou F, Lipshutz BH. Amide and Peptide Bond Formation in Water at Room Temperature. Organic Letters. 17: 3968-71. PMID 26251952 DOI: 10.1021/Acs.Orglett.5B01812 |
0.369 |
|
| 2015 |
Bhattacharjya A, Klumphu P, Lipshutz BH. Kumada-Grignard-type biaryl couplings on water. Nature Communications. 6: 7401. PMID 26084774 DOI: 10.1038/Ncomms8401 |
0.424 |
|
| 2015 |
Bhattacharjya A, Klumphu P, Lipshutz BH. Ligand-free, palladium-catalyzed dihydrogen generation from TMDS: dehalogenation of aryl halides on water. Organic Letters. 17: 1122-5. PMID 25679825 DOI: 10.1021/Ol5037369 |
0.453 |
|
| 2015 |
Isley NA, Hageman MS, Lipshutz BH. Dehalogenation of Functionalized Alkyl Halides in Water at Room Temperature. Green Chemistry : An International Journal and Green Chemistry Resource : Gc. 2015: 307. PMID 25530711 DOI: 10.1039/C4Gc01733A |
0.402 |
|
| 2015 |
Krasovskiy AL, Haley S, Voigtritter K, Lipshutz BH. ChemInform Abstract: Stereoretentive Pd-Catalyzed Kumada-Corriu Couplings of Alkenyl Halides at Room Temperature. Cheminform. 46: no-no. DOI: 10.1002/chin.201507063 |
0.768 |
|
| 2014 |
Slack ED, Gabriel CM, Lipshutz BH. A palladium nanoparticle-nanomicelle combination for the stereoselective semihydrogenation of alkynes in water at room temperature. Angewandte Chemie (International Ed. in English). 53: 14051-4. PMID 25323663 DOI: 10.1002/Anie.201407723 |
0.392 |
|
| 2014 |
Lipshutz BH, Ghorai S. Transitioning organic synthesis from organic solvents to water. What's your E Factor? Green Chemistry : An International Journal and Green Chemistry Resource : Gc. 16: 3660-3679. PMID 25170307 DOI: 10.1039/C4Gc00503A |
0.344 |
|
| 2014 |
Lipshutz BH, Hageman M, Fennewald JC, Linstadt R, Slack E, Voigtritter K. Selective oxidations of activated alcohols in water at room temperature. Chemical Communications (Cambridge, England). 50: 11378-81. PMID 25126656 DOI: 10.1039/C4Cc05163G |
0.755 |
|
| 2014 |
Handa S, Lippincott DJ, Aue DH, Lipshutz BH. Asymmetric gold-catalyzed lactonizations in water at room temperature. Angewandte Chemie (International Ed. in English). 53: 10658-62. PMID 25124085 DOI: 10.1002/Anie.201404729 |
0.443 |
|
| 2014 |
Krasovskiy AL, Haley S, Voigtritter K, Lipshutz BH. Stereoretentive Pd-catalyzed Kumada-Corriu couplings of alkenyl halides at room temperature. Organic Letters. 16: 4066-9. PMID 25102436 DOI: 10.1021/Ol501535W |
0.801 |
|
| 2014 |
Isley NA, Linstadt RT, Slack ED, Lipshutz BH. Copper-catalyzed hydrophosphinations of styrenes in water at room temperature. Dalton Transactions (Cambridge, England : 2003). 43: 13196-200. PMID 25058397 DOI: 10.1039/C4Dt00993B |
0.369 |
|
| 2014 |
Isley NA, Dobarco S, Lipshutz BH. Installation of protected ammonia equivalents onto aromatic & heteroaromatic rings in water enabled by micellar catalysis. Green Chemistry : An International Journal and Green Chemistry Resource : Gc. 16: 1480-1488. PMID 25018667 DOI: 10.1039/C3Gc42188K |
0.454 |
|
| 2014 |
Fennewald JC, Lipshutz BH. Trifluoromethylation of Heterocycles in Water at Room Temperature. Green Chemistry : An International Journal and Green Chemistry Resource : Gc. 16: 1097-1100. PMID 24839397 DOI: 10.1039/C3Gc42119H |
0.38 |
|
| 2014 |
Linstadt RT, Peterson CA, Lippincott DJ, Jette CI, Lipshutz BH. Stereoselective silylcupration of conjugated alkynes in water at room temperature. Angewandte Chemie (International Ed. in English). 53: 4159-63. PMID 24643966 DOI: 10.1002/Anie.201311035 |
0.491 |
|
| 2014 |
Handa S, Fennewald JC, Lipshutz BH. Aerobic oxidation in nanomicelles of aryl alkynes, in water at room temperature. Angewandte Chemie (International Ed. in English). 53: 3432-5. PMID 24616243 DOI: 10.1002/Anie.201310634 |
0.327 |
|
| 2014 |
Klumphu P, Lipshutz BH. "Nok": a phytosterol-based amphiphile enabling transition-metal-catalyzed couplings in water at room temperature. The Journal of Organic Chemistry. 79: 888-900. PMID 24447127 DOI: 10.1021/Jo401744B |
0.34 |
|
| 2014 |
Minkler SR, Isley NA, Lippincott DJ, Krause N, Lipshutz BH. Leveraging the micellar effect: gold-catalyzed dehydrative cyclizations in water at room temperature. Organic Letters. 16: 724-6. PMID 24433154 DOI: 10.1021/Ol403402H |
0.443 |
|
| 2014 |
Kelly SM, Lipshutz BH. Chemoselective reductions of nitroaromatics in water at room temperature. Organic Letters. 16: 98-101. PMID 24341483 DOI: 10.1021/Ol403079X |
0.356 |
|
| 2014 |
Yang F, Klumphu P, Liang YM, Lipshutz BH. Copper-catalyzed trifluoromethylation of N-arylacrylamides "on water" at room temperature. Chemical Communications (Cambridge, England). 50: 936-8. PMID 24306078 DOI: 10.1039/C3Cc48131J |
0.416 |
|
| 2013 |
Lipshutz BH, Boškovi? Z, Crowe CS, Davis VK, Whittemore HC, Vosburg DA, Wenzel AG. "Click" and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles. Journal of Chemical Education. 90. PMID 24324282 DOI: 10.1021/Ed300893U |
0.435 |
|
| 2013 |
Isley NA, Gallou F, Lipshutz BH. Transforming Suzuki-Miyaura cross-couplings of MIDA boronates into a green technology: no organic solvents. Journal of the American Chemical Society. 135: 17707-10. PMID 24224801 DOI: 10.1021/Ja409663Q |
0.398 |
|
| 2013 |
Lipshutz BH, Isley NA, Fennewald JC, Slack ED. On the way towards greener transition-metal-catalyzed processes as quantified by E factors. Angewandte Chemie (International Ed. in English). 52: 10952-8. PMID 24030905 DOI: 10.1002/Anie.201302020 |
0.384 |
|
| 2013 |
Lu GP, Cai C, Lipshutz BH. Stille couplings in water at room temperature Green Chemistry. 15: 105-109. DOI: 10.1039/C2Gc36042J |
0.348 |
|
| 2012 |
Lipshutz BH, Isley NA, Moser R, Ghorai S, Leuser H, Taft BR. Rhodium-Catalyzed Asymmetric 1,4-Additions, in Water at Room Temperature, with In-Flask Catalyst Recycling. Advanced Synthesis & Catalysis. 354: 3175-3179. PMID 24659941 DOI: 10.1002/Adsc.201200160 |
0.818 |
|
| 2012 |
Lipshutz BH, Taft BR, Abela AR, Ghorai S, Krasovskiy A, Duplais C. Catalysis in the Service of Green Chemistry: Nobel Prize-Winning Palladium-Catalysed Cross-Couplings, Run in Water at Room Temperature: Heck, Suzuki-Miyaura and Negishi reactions carried out in the absence of organic solvents, enabled by micellar catalysis. Platinum Metals Review. 56: 62-74. PMID 23555153 DOI: 10.1595/147106712X629761 |
0.813 |
|
| 2012 |
Lipshutz BH, Huang S, Leong WW, Zhong G, Isley NA. C-C bond formation via copper-catalyzed conjugate addition reactions to enones in water at room temperature. Journal of the American Chemical Society. 134: 19985-8. PMID 23190029 DOI: 10.1021/Ja309409E |
0.622 |
|
| 2012 |
Lu GP, Voigtritter KR, Cai C, Lipshutz BH. Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halides. Chemical Communications (Cambridge, England). 48: 8661-3. PMID 22822482 DOI: 10.1039/C2Cc33294A |
0.818 |
|
| 2012 |
Lu GP, Voigtritter KR, Cai C, Lipshutz BH. Ligand effects on the stereochemical outcome of Suzuki-Miyaura couplings. The Journal of Organic Chemistry. 77: 3700-3. PMID 22480237 DOI: 10.1021/Jo300437T |
0.802 |
|
| 2012 |
Moser R, Ghorai S, Lipshutz BH. Modified routes to the "designer" surfactant PQS. The Journal of Organic Chemistry. 77: 3143-8. PMID 22413960 DOI: 10.1021/Jo202564B |
0.602 |
|
| 2012 |
Lipshutz BH, Ghorai S. Organocatalysis in water at room temperature with in-flask catalyst recycling. Organic Letters. 14: 422-5. PMID 22182221 DOI: 10.1021/Ol203242R |
0.381 |
|
| 2012 |
Voigtritter KR, Isley NA, Moser R, Aue DH, Lipshutz BH. Regioselective reductions of β,β-disubstituted enones catalyzed by nonracemically ligated copper hydride Tetrahedron. 68: 3410-3416. DOI: 10.1016/J.Tet.2011.10.056 |
0.791 |
|
| 2011 |
Duplais C, Krasovskiy A, Lipshutz BH. Organozinc Chemistry Enabled by Micellar Catalysis. Palladium-Catalyzed Cross-Couplings between Alkyl and Aryl Bromides in Water at Room Temperature. Organometallics. 30: 6090-6097. PMID 23539206 DOI: 10.1021/Om200846H |
0.758 |
|
| 2011 |
Krasovskiy A, Lipshutz BH. Ligand effects on Negishi couplings of alkenyl halides. Organic Letters. 13: 3818-21. PMID 21739948 DOI: 10.1021/Ol2010165 |
0.392 |
|
| 2011 |
Krasovskiy A, Lipshutz BH. Highly selective reactions of unbiased alkenyl halides and alkylzinc halides: Negishi-Plus couplings. Organic Letters. 13: 3822-5. PMID 21739947 DOI: 10.1021/Ol201307Y |
0.473 |
|
| 2011 |
Krasovskaya V, Krasovskiy A, Lipshutz BH. Synthesis of unsymmetrical arylheteroarylmethanes by direct "on water" cross-coupling between benzylic and heteroaromatic halides. Chemistry, An Asian Journal. 6: 1974-6. PMID 21626709 DOI: 10.1002/Asia.201100153 |
0.401 |
|
| 2011 |
Lipshutz BH, Ghorai S, Abela AR, Moser R, Nishikata T, Duplais C, Krasovskiy A, Gaston RD, Gadwood RC. TPGS-750-M: a second-generation amphiphile for metal-catalyzed cross-couplings in water at room temperature. The Journal of Organic Chemistry. 76: 4379-91. PMID 21548658 DOI: 10.1021/Jo101974U |
0.83 |
|
| 2011 |
Lipshutz BH, Ghorai S, Leong WW, Taft BR, Krogstad DV. Manipulating micellar environments for enhancing transition metal-catalyzed cross-couplings in water at room temperature. The Journal of Organic Chemistry. 76: 5061-73. PMID 21539384 DOI: 10.1021/Jo200746Y |
0.78 |
|
| 2011 |
Voigtritter K, Ghorai S, Lipshutz BH. Rate enhanced olefin cross-metathesis reactions: the copper iodide effect. The Journal of Organic Chemistry. 76: 4697-702. PMID 21528868 DOI: 10.1021/Jo200360S |
0.82 |
|
| 2011 |
Krasovskaya V, Krasovskiy A, Bhattacharjya A, Lipshutz BH. "On water" sp3-sp2 cross-couplings between benzylic and alkenyl halides. Chemical Communications (Cambridge, England). 47: 5717-9. PMID 21487612 DOI: 10.1039/C1Cc11087J |
0.432 |
|
| 2011 |
Krasovskiy A, Thomé I, Graff J, Krasovskaya V, Konopelski P, Duplais C, Lipshutz BH. Cross-couplings of alkyl halides with heteroaromatic halides, in water at room temperature Tetrahedron Letters. 52: 2203-2205. DOI: 10.1016/J.Tetlet.2010.11.160 |
0.737 |
|
| 2011 |
Voigtritter K, Ghorai S, Lipshutz BH. ChemInform Abstract: Rate Enhanced Olefin Cross-Metathesis Reactions: The Copper Iodide Effect. Cheminform. 42: no-no. DOI: 10.1002/chin.201136040 |
0.784 |
|
| 2011 |
Krasovskiy A, Thome I, Graff J, Krasovskaya V, Konopelski P, Duplais C, Lipshutz BH. ChemInform Abstract: Cross-Coupling of Alkyl Halides with Heteroaromatic Halides, in Water at Room Temperature. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201130093 |
0.697 |
|
| 2011 |
Lipshutz BH, Abela AR, Boskovic ZV, Nishikata T, Duplais C, Krasovskiy A. ChemInform Abstract: “Greening Up” Cross-Coupling Chemistry Cheminform. 42: no-no. DOI: 10.1002/chin.201105250 |
0.796 |
|
| 2010 |
Lipshutz BH, Moser R, Voigtritter KR. Miyaura Borylations of Aryl Bromides in Water at Room Temperature. Israel Journal of Chemistry. 50: 691-695. PMID 24761030 DOI: 10.1002/Ijch.201000045 |
0.819 |
|
| 2010 |
Krasovskiy A, Duplais C, Lipshutz BH. Stereoselective Negishi-like couplings between alkenyl and alkyl halides in water at room temperature. Organic Letters. 12: 4742-4. PMID 20882969 DOI: 10.1021/Ol101885T |
0.719 |
|
| 2010 |
Huang S, Petersen TB, Lipshutz BH. Total synthesis of (+)-korupensamine B via an atropselective intermolecular biaryl coupling. Journal of the American Chemical Society. 132: 14021-3. PMID 20849111 DOI: 10.1021/Ja1065202 |
0.803 |
|
| 2010 |
Moser R, Boskovi? ZV, Crowe CS, Lipshutz BH. CuH-catalyzed enantioselective 1,2-reductions of alpha,beta-unsaturated ketones. Journal of the American Chemical Society. 132: 7852-3. PMID 20481528 DOI: 10.1021/Ja102689E |
0.624 |
|
| 2010 |
Nishikata T, Lipshutz BH. Cationic Pd(II)-catalyzed Fujiwara-Moritani reactions at room temperature in water. Organic Letters. 12: 1972-5. PMID 20364834 DOI: 10.1021/Ol100331H |
0.379 |
|
| 2010 |
Nishikata T, Abela AR, Huang S, Lipshutz BH. Cationic palladium(II) catalysis: C-H activation/Suzuki-Miyaura couplings at room temperature. Journal of the American Chemical Society. 132: 4978-9. PMID 20307066 DOI: 10.1021/Ja910973A |
0.815 |
|
| 2010 |
Duplais C, Forman AJ, Baker BA, Lipshutz BH. UC Pd: a new form of Pd/C for Sonogashira couplings. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3366-71. PMID 20140914 DOI: 10.1002/Chem.200902471 |
0.695 |
|
| 2010 |
Duplais C, Krasovskiy A, Wattenberg A, Lipshutz BH. Cross-couplings between benzylic and aryl halides "on water": synthesis of diarylmethanes. Chemical Communications (Cambridge, England). 46: 562-4. PMID 20062862 DOI: 10.1039/B922280D |
0.753 |
|
| 2010 |
Nishikata T, Abela AR, Lipshutz BH. Room temperature C-H activation and cross-coupling of aryl ureas in water. Angewandte Chemie (International Ed. in English). 49: 781-4. PMID 20025011 DOI: 10.1002/Anie.200905967 |
0.827 |
|
| 2010 |
Moser R, Nishikata T, Lipshutz BH. Pd-catalyzed synthesis of allylic silanes from allylic ethers. Organic Letters. 12: 28-31. PMID 19950911 DOI: 10.1021/Ol9023908 |
0.646 |
|
| 2010 |
Huang S, Voigtritter KR, Unger JB, Lipshutz BH. Asymmetric CuH-catalyzed 1,4-reductions in water at room temperature Synlett. 2041-2044. DOI: 10.1055/S-0030-1258540 |
0.794 |
|
| 2010 |
Duplais C, Forman AJ, Baker BA, Lipshutz BH. Sonogashira Coupling with UC Pd under Copper-Free Conditions Synfacts. 2010: 729-729. DOI: 10.1055/S-0029-1219898 |
0.693 |
|
| 2010 |
Lee C-, Huang S, Lipshutz BH. Tandem One-Pot Diazo Transfer-Click Reactions UsingCu/C as a Catalyst Synfacts. 2010: 371-371. DOI: 10.1055/S-0029-1219284 |
0.389 |
|
| 2010 |
Deutsch C, Lipshutz BH, Krause N. Copper-Catalyzed SN2′ Reduction of PropargylicCarbonates Synfacts. 2010: 183-183. DOI: 10.1055/S-0029-1219095 |
0.391 |
|
| 2010 |
Lipshutz BH, Ghorai S. PQS-2: ring-closing- and cross-metathesis reactions on lipophilic substrates; in water only at room temperature, with in-flask catalyst recycling Tetrahedron. 66: 1057-1063. DOI: 10.1016/J.Tet.2009.11.010 |
0.442 |
|
| 2010 |
Lipshutz BH, Abela AR, Boškovi? ZV, Nishikata T, Duplais C, Krasovskiy A. "Greening up" cross-coupling chemistry Topics in Catalysis. 53: 985-990. DOI: 10.1007/S11244-010-9537-1 |
0.83 |
|
| 2010 |
Huang S, Voigtritter KR, Unger JB, Lipshutz BH. ChemInform Abstract: Asymmetric CuH-Catalyzed 1,4-Reductions in Water at Room Temperature. Cheminform. 41: no-no. DOI: 10.1002/chin.201048033 |
0.803 |
|
| 2010 |
LIPSHUTZ BH, BHANDARI A, LINDSLEY C, KEIL R, WOOD MR. ChemInform Abstract: New Synthetic Methods Based on Organozirconium and Organocopper Chemistry Cheminform. 25: no-no. DOI: 10.1002/chin.199442296 |
0.352 |
|
| 2010 |
Abela AR, Huang S, Moser R, Lipshutz BH. Sustainability getting organic solvents out of organic reactions Chimica Oggi. 28: 50-53. |
0.745 |
|
| 2009 |
Lipshutz BH, Chung DW, Rich B. Aminations of Aryl Bromides in Water at Room Temperature. Advanced Synthesis & Catalysis. 351: 1717-1721. PMID 21804786 DOI: 10.1002/Adsc.200900323 |
0.61 |
|
| 2009 |
Gallagher BD, Taft BR, Lipshutz BH. Asymmetric conjugate reductions of coumarins. A new route to tolterodine and related coumarin derivatives. Organic Letters. 11: 5374-7. PMID 19877705 DOI: 10.1021/Ol9020404 |
0.738 |
|
| 2009 |
Deutsch C, Lipshutz BH, Krause N. (NHC)CuH-catalyzed entry to allenes via propargylic carbonate S(N)2'-reductions. Organic Letters. 11: 5010-2. PMID 19863153 DOI: 10.1021/Ol901868M |
0.364 |
|
| 2009 |
Nishikata T, Lipshutz BH. Aminations of allylic phenyl ethers via micellar catalysis at room temperature in water. Chemical Communications (Cambridge, England). 6472-4. PMID 19841813 DOI: 10.1039/B914982A |
0.408 |
|
| 2009 |
Krasovskiy A, Duplais C, Lipshutz BH. Zn-mediated, Pd-catalyzed cross-couplings in water at room temperature without prior formation of organozinc reagents. Journal of the American Chemical Society. 131: 15592-3. PMID 19827762 DOI: 10.1021/Ja906803T |
0.725 |
|
| 2009 |
Nishikata T, Lipshutz BH. Allylic ethers as educts for Suzuki-Miyaura couplings in water at room temperature. Journal of the American Chemical Society. 131: 12103-5. PMID 19663513 DOI: 10.1021/Ja905082C |
0.395 |
|
| 2009 |
Nishikata T, Lipshutz BH. Amination of allylic alcohols in water at room temperature. Organic Letters. 11: 2377-9. PMID 19402681 DOI: 10.1021/Ol900235S |
0.378 |
|
| 2009 |
Lipshutz BH, Ghorai S, Leong WW. Deprotection of homoallyl ((h)Allyl) derivatives of phenols, alcohols, acids, and amines. The Journal of Organic Chemistry. 74: 2854-7. PMID 19278206 DOI: 10.1021/Jo900012Z |
0.32 |
|
| 2009 |
Lipshutz BH, Amorelli B. Total synthesis of piericidin A1. Application of a modified Negishi carboalumination-nickel-catalyzed cross-coupling. Journal of the American Chemical Society. 131: 1396-7. PMID 19138148 DOI: 10.1021/Ja809542R |
0.359 |
|
| 2009 |
Lipshutz BH, Ghorai S. PQS: a new platform for micellar catalysis. RCM reactions in water, with catalyst recycling. Organic Letters. 11: 705-8. PMID 19105682 DOI: 10.1021/Ol8027829 |
0.413 |
|
| 2009 |
Lipshutz BH. Rediscovering organocopper chemistry through copper hydride. It's all about the ligand Synlett. 509-524. DOI: 10.1055/S-0028-1087923 |
0.383 |
|
| 2009 |
Lipshutz BH, Boškovič ŽV, Aue DH. Synthesis of Alkenylboronates via Hydrocupration/Transmetalation Synfacts. 2009: 320-320. DOI: 10.1055/S-0028-1087708 |
0.337 |
|
| 2009 |
Taft BR, Swift EC, Lipshutz BH. A convenient preparation of di-p-chlorobenzyl azodicarboxylate (DCAD) for mitsunobu couplings Synthesis. 332-334. DOI: 10.1055/S-0028-1083274 |
0.743 |
|
| 2009 |
Nulwala H, Takizawa K, Odukale A, Khan A, Thibault RJ, Taft BR, Lipshutz BH, Hawker CJ. Synthesis and characterization of isomeric vinyl-1,2,3-triazole materials by azide - Alkyne click chemistry Macromolecules. 42: 6068-6074. DOI: 10.1021/Ma900892H |
0.76 |
|
| 2009 |
Lipshutz BH, Amorelli B. Carboalumination/Ni-catalyzed couplings. A short synthesis of verticipyrone Tetrahedron Letters. 50: 2144-2146. DOI: 10.1016/J.Tetlet.2009.02.167 |
0.481 |
|
| 2009 |
Lee C, Huang S, Lipshutz B. Copper-in-Charcoal-Catalyzed, Tandem One-Pot Diazo Transfer-Click Reactions Advanced Synthesis & Catalysis. 351: 3139-3142. DOI: 10.1002/Adsc.200900604 |
0.72 |
|
| 2008 |
Lipshutz BH, Boskovi? ZV, Aue DH. Synthesis of activated alkenylboronates from acetylenic esters by CuH-catalyzed 1,2-addition/transmetalation. Angewandte Chemie (International Ed. in English). 47: 10183-6. PMID 19034937 DOI: 10.1002/Anie.200804912 |
0.406 |
|
| 2008 |
Lipshutz BH, Abela AR. Micellar catalysis of Suzuki-Miyaura cross-couplings with heteroaromatics in water. Organic Letters. 10: 5329-32. PMID 18998705 DOI: 10.1021/Ol801712E |
0.796 |
|
| 2008 |
Lipshutz BH, Amorelli B, Unger JB. CuH-catalyzed enantioselective intramolecular reductive aldol reactions generating three new contiguous asymmetric stereocenters. Journal of the American Chemical Society. 130: 14378-9. PMID 18847266 DOI: 10.1021/Ja8045475 |
0.643 |
|
| 2008 |
Lipshutz BH, Nihan DM, Vinogradova E, Taft BR, Bosković ZV. Copper + nickel-in-charcoal (Cu-Ni/C): a bimetallic, heterogeneous catalyst for cross-couplings. Organic Letters. 10: 4279-82. PMID 18763793 DOI: 10.1021/Ol801676U |
0.83 |
|
| 2008 |
Lee CT, Lipshutz BH. Nonracemic diarylmethanols from CuH-catalyzed hydrosilylation of diaryl ketones. Organic Letters. 10: 4187-90. PMID 18754623 DOI: 10.1021/Ol801590J |
0.608 |
|
| 2008 |
Lipshutz BH, Chung DW, Rich B. Sonogashira couplings of aryl bromides: room temperature, water only, no copper. Organic Letters. 10: 3793-6. PMID 18683937 DOI: 10.1021/Ol801471F |
0.661 |
|
| 2008 |
Wraight CA, Vakkasoglu AS, Poluektov Y, Mattis AJ, Nihan D, Lipshutz BH. The 2-methoxy group of ubiquinone is essential for function of the acceptor quinones in reaction centers from Rba. sphaeroides. Biochimica Et Biophysica Acta. 1777: 631-6. PMID 18474215 DOI: 10.1016/J.Bbabio.2008.04.025 |
0.764 |
|
| 2008 |
Lipshutz BH, Aguinaldo GT, Ghorai S, Voigtritter K. Olefin cross-metathesis reactions at room temperature using the nonionic amphiphile "PTS": just add water. Organic Letters. 10: 1325-8. PMID 18335947 DOI: 10.1021/Ol800028X |
0.799 |
|
| 2008 |
Lipshutz BH, Taft BR. Heck couplings at room temperature in nanometer aqueous micelles. Organic Letters. 10: 1329-32. PMID 18335945 DOI: 10.1021/Ol702755G |
0.727 |
|
| 2008 |
Lipshutz BH, Petersen TB, Abela AR. Room-temperature Suzuki-Miyaura couplings in water facilitated by nonionic amphiphiles. Organic Letters. 10: 1333-6. PMID 18335944 DOI: 10.1021/Ol702714Y |
0.809 |
|
| 2008 |
Lipshutz BH, Butler T, Swift E. C-C bond formation catalyzed heterogeneously by nickel-on-graphite (Ni/Cg). Organic Letters. 10: 697-700. PMID 18269286 DOI: 10.1021/Ol702453Q |
0.402 |
|
| 2008 |
Baker BA, Boskovi? ZV, Lipshutz BH. (BDP)CuH: a "hot" Stryker's reagent for use in achiral conjugate reductions. Organic Letters. 10: 289-92. PMID 18092793 DOI: 10.1021/Ol702689V |
0.382 |
|
| 2008 |
Butler TA, Swift EC, Lipshutz BH. Heterogeneous catalysis with nickel-on-graphite (Ni/Cg). Organic & Biomolecular Chemistry. 6: 19-25. PMID 18075642 DOI: 10.1039/B714600K |
0.43 |
|
| 2008 |
Baker BA, Boskovic ZV, Lipshutz BH. (BDP)CuH: A Highly Active Reagent for Achiral Conjugate Reductions Synfacts. 2008: 413-413. DOI: 10.1055/S-2008-1042824 |
0.321 |
|
| 2008 |
Lipshutz BH, Ghorai S, Boškovi? ZV. Tandem olefin metathesis-elimination reactions. A new route to doubly unsaturated carbonyl derivatives Tetrahedron. 64: 6949-6954. DOI: 10.1016/J.Tet.2008.04.027 |
0.403 |
|
| 2008 |
Lipshutz BH, Aguinaldo GT, Ghorai S, Voigtritter K. ChemInform Abstract: Olefin Cross-Metathesis Reactions at Room Temperature Using the Nonionic Amphiphile “PTS”: Just Add Water. Cheminform. 39. DOI: 10.1002/chin.200834045 |
0.78 |
|
| 2008 |
Lipshutz BH, Ghorai S, Aguinaldo GT. Ring-closing metathesis at room temperature within nanometer micelles using water as the only solvent Advanced Synthesis and Catalysis. 350: 953-956. DOI: 10.1002/Adsc.200800114 |
0.357 |
|
| 2007 |
Lipshutz BH, Lee CT, Servesko JM. Asymmetric CuH-catalyzed hydrosilylations en route to the C-9 epimer of amphidinoketide iota. Organic Letters. 9: 4713-6. PMID 17949006 DOI: 10.1021/Ol701999H |
0.787 |
|
| 2007 |
Lipshutz BH, Butler T, Lower A, Servesko J. Enhancing regiocontrol in carboaluminations of terminal alkynes. Application to the one-pot synthesis of coenzyme Q10. Organic Letters. 9: 3737-40. PMID 17705500 DOI: 10.1021/Ol701469E |
0.78 |
|
| 2007 |
Lipshutz BH, Unger JB, Taft BR. Copper-in-charcoal (Cu/C) promoted diaryl ether formation. Organic Letters. 9: 1089-92. PMID 17305352 DOI: 10.1021/Ol0700409 |
0.812 |
|
| 2007 |
Deutsch C, Lipshutz BH, Krause N. Small but effective: copper hydride catalyzed synthesis of alpha-hydroxyallenes. Angewandte Chemie (International Ed. in English). 46: 1650-3. PMID 17221896 DOI: 10.1002/Anie.200603739 |
0.336 |
|
| 2007 |
Lipshutz BH, Lee CT, Taft BR. A conjugate reduction pathway to chiral silanes using CuH Synthesis. 3257-3260. DOI: 10.1055/S-2007-983830 |
0.779 |
|
| 2007 |
Krause N, Deutsch C, Lipshutz B. Copper-Catalyzed SN2′ Reduction of Propargyl Oxiranes Synfacts. 2007: 0493-0493. DOI: 10.1055/S-2007-968439 |
0.397 |
|
| 2007 |
Lipshutz B, Butler T, Lower A. Regioselective Negishi Carboaluminations Synfacts. 2007: 0277-0277. DOI: 10.1055/S-2007-968269 |
0.721 |
|
| 2006 |
Lipshutz BH, Frieman BA, Lee CT, Lower A, Nihan DM, Taft BR. Microwave-assisted heterogeneous cross-coupling reactions catalyzed by nickel-in-charcoal (Ni/C). Chemistry, An Asian Journal. 1: 417-29. PMID 17441078 DOI: 10.1002/Asia.200600031 |
0.817 |
|
| 2006 |
Lipshutz BH, Butler T, Lower A. Controlling regiochemistry in Negishi carboaluminations. Fine tuning the ligand on zirconium. Journal of the American Chemical Society. 128: 15396-8. PMID 17132005 DOI: 10.1021/Ja065769B |
0.673 |
|
| 2006 |
Lipshutz BH, Taft BR. Heterogeneous copper-in-charcoal-catalyzed click chemistry. Angewandte Chemie (International Ed. in English). 45: 8235-8. PMID 17111447 DOI: 10.1002/Anie.200603726 |
0.75 |
|
| 2006 |
Lipshutz BH, Chung DW, Rich B, Corral R. Simplification of the Mitsunobu reaction. Di-p-chlorobenzyl azodicarboxylate: a new azodicarboxylate. Organic Letters. 8: 5069-72. PMID 17048845 DOI: 10.1021/Ol0618757 |
0.596 |
|
| 2006 |
Lipshutz BH, Lower A, Kucejko RJ, Noson K. Applications of asymmetric hydrosilylations mediated by catalytic (DTBM-SEGPHOS)CuH. Organic Letters. 8: 2969-72. PMID 16805529 DOI: 10.1021/Ol060854+ |
0.817 |
|
| 2006 |
Lipshutz BH, Tanaka N, Taft BR, Lee CT. Chiral silanes via asymmetric hydrosilylation with catalytic CuH. Organic Letters. 8: 1963-6. PMID 16671757 DOI: 10.1021/Ol0529593 |
0.793 |
|
| 2006 |
Lipshutz BH, Frieman BA, Tomaso AE. Copper-in-charcoal (Cu/C): heterogeneous, copper-catalyzed asymmetric hydrosilylations. Angewandte Chemie (International Ed. in English). 45: 1259-64. PMID 16425315 DOI: 10.1002/Anie.200503149 |
0.763 |
|
| 2006 |
Lipshutz BH, Frieman BA, Butler T, Kogan V. Heterogeneous catalysis with nickel-on-graphite (Ni/C(g)): reduction of aryl tosylates and mesylates. Angewandte Chemie (International Ed. in English). 45: 800-3. PMID 16370015 DOI: 10.1002/Anie.200502887 |
0.758 |
|
| 2006 |
Lipshutz BH, Butler T, Frieman BA, Kogan V, Lee CT, Lower A, Nihan DM, Taft BR, Tomaso AE. New technologies in catalysis using base metals Pure and Applied Chemistry. 78: 377-384. DOI: 10.1351/Pac200678020377 |
0.773 |
|
| 2006 |
Lipshutz B, Lower A, Kucejko R, Noson K. Cu-Catalyzed Asymmetric Hydrosilylations of Ketones Synfacts. 2006: 0935-0935. DOI: 10.1055/S-2006-949212 |
0.798 |
|
| 2006 |
Lipshutz BH, Butler T, Frieman BA, Kogan V, Lee C, Lower A, Nihan DM, Taft BR, Tomaso AEJ. New Technologies in Catalysis Using Base Metals Cheminform. 37. DOI: 10.1002/chin.200631253 |
0.459 |
|
| 2006 |
Lipshutz BH, Frieman BA, Unger JB, Nihan DM. Thermally Accelerated Asymmetric Hydrosilylations Using Ligated Copper Hydride. Cheminform. 37. DOI: 10.1002/chin.200612029 |
0.567 |
|
| 2005 |
Lipshutz BH, Clososki GC, Chrisman W, Chung DW, Ball DB, Howell J. New conjunctive reagents as cross-coupling partners en route to retinoid-like polyenes. Organic Letters. 7: 4561-4. PMID 16209479 DOI: 10.1021/Ol051406P |
0.812 |
|
| 2005 |
Lipshutz BH, Lower A, Berl V, Schein K, Wetterich F. An improved synthesis of the "miracle nutrient" coenzyme Q10. Organic Letters. 7: 4095-7. PMID 16146360 DOI: 10.1021/Ol051329Y |
0.724 |
|
| 2005 |
Lipshutz BH, Frieman BA. CuH in a bottle: a convenient reagent for asymmetric hydrosilylations. Angewandte Chemie (International Ed. in English). 44: 6345-8. PMID 16124024 DOI: 10.1055/S-2005-921738 |
0.799 |
|
| 2005 |
Lipshutz BH, Frieman BA, Unger JB, Nihan DM. Thermally accelerated asymmetric hydrosilylations using ligated copper hydride Canadian Journal of Chemistry. 83: 606-614. DOI: 10.1139/V05-083 |
0.793 |
|
| 2005 |
Frieman BA, Taft BR, Lee CT, Butler T, Lipshutz BH. Nickel-in-charcoal (Ni/C): An efficient heterogeneous catalyst for the construction of C-C, C-N, and C-H bonds Synthesis. 2989-2993. DOI: 10.1055/S-2005-872145 |
0.799 |
|
| 2005 |
Lipshutz BH, Frieman BA. Cover Picture: CuH in a Bottle: A Convenient Reagent for Asymmetric Hydrosilylations (Angew. Chem. Int. Ed. 39/2005) Angewandte Chemie International Edition. 44: 6253-6253. DOI: 10.1002/Anie.200590130 |
0.758 |
|
| 2005 |
Lipshutz BH, Frieman BA. Titelbild: CuH in a Bottle: A Convenient Reagent for Asymmetric Hydrosilylations (Angew. Chem. 39/2005) Angewandte Chemie. 117: 6409-6409. DOI: 10.1002/Ange.200590130 |
0.797 |
|
| 2004 |
Lipshutz BH, Servesko JM, Taft BR. Asymmetric 1,4-hydrosilylations of alpha,beta-unsaturated esters. Journal of the American Chemical Society. 126: 8352-3. PMID 15237972 DOI: 10.1021/Ja049135L |
0.783 |
|
| 2004 |
Lipshutz BH, Frieman B, Birkedal H. Scavenging and reclaiming phosphines associated with group 10 metal-mediated couplings. Organic Letters. 6: 2305-8. PMID 15228265 DOI: 10.1021/Ol049681J |
0.785 |
|
| 2004 |
Lipshutz BH, Shimizu H. Copper(I)-catalyzed asymmetric hydrosilylations of imines at ambient temperatures. Angewandte Chemie (International Ed. in English). 43: 2228-30. PMID 15108129 DOI: 10.1002/Anie.200353294 |
0.386 |
|
| 2004 |
Lipshutz BH, Servesko JM, Petersen TB, Papa PP, Lover AA. Asymmetric 1,4-reductions of hindered beta-substituted cycloalkenones using catalytic SEGPHOS-ligated CuH. Organic Letters. 6: 1273-5. PMID 15070315 DOI: 10.1021/Ol0400185 |
0.812 |
|
| 2004 |
Lipshutz BH, Buzard DJ, Olsson C, Noson K. A modular route to nonracemic cyclo-NOBINs. Preparation of the parent ligand for homo- and heterogeneous catalysis Tetrahedron. 60: 4443-4449. DOI: 10.1016/J.Tet.2004.02.065 |
0.776 |
|
| 2004 |
Lipshutz BH, Frieman B. Microwave accelerated, Ni/C-catalyzed cross-couplings of in situ-derived zirconocenes Tetrahedron. 60: 1309-1316. DOI: 10.1016/J.Tet.2003.10.029 |
0.803 |
|
| 2004 |
Lipshutz BH, Servesko JM, Taft BR. Asymmetric 1,4-Hydrosilylations of α,β-Unsaturated Esters. Cheminform. 35. DOI: 10.1002/chin.200445024 |
0.755 |
|
| 2004 |
Lipshutz BH, Frieman B. Microwave-Accelerated, Ni/C-Catalyzed Cross-Couplings of in situ-Derived Zirconocenes. Cheminform. 35. DOI: 10.1002/chin.200422093 |
0.776 |
|
| 2004 |
Lipshutz BH, Sengupta S. Organocopper Reagents: Substitution, Conjugate Addition, Carbo/Metallocupration, and Other Reactions Organic Reactions. DOI: 10.1002/0471264180.Or041.02 |
0.462 |
|
| 2003 |
Lipshutz BH, Servesko JM. CuH-catalyzed asymmetric conjugate reductions of acyclic enones. Angewandte Chemie (International Ed. in English). 42: 4789-92. PMID 14562350 DOI: 10.1002/Anie.200352313 |
0.821 |
|
| 2003 |
Lipshutz BH, Caires CC, Kuipers P, Chrisman W. Tweaking copper hydride (CuH) for synthetic gain. A practical, one-pot conversion of dialkyl ketones to reduced trialkylsilyl ether derivatives. Organic Letters. 5: 3085-8. PMID 12916987 DOI: 10.1021/Ol035164+ |
0.796 |
|
| 2003 |
Lipshutz BH, Noson K, Chrisman W, Lower A. Asymmetric hydrosilylation of aryl ketones catalyzed by copper hydride complexed by nonracemic biphenyl bis-phosphine ligands. Journal of the American Chemical Society. 125: 8779-89. PMID 12862472 DOI: 10.1021/Ja021391F |
0.817 |
|
| 2003 |
Tasler S, Lipshutz BH. Nickel-on-charcoal-catalyzed aromatic aminations and Kumada couplings: mechanistic and synthetic aspects. The Journal of Organic Chemistry. 68: 1190-9. PMID 12585855 DOI: 10.1021/Jo020297E |
0.477 |
|
| 2003 |
Lipshutz BH, Tasler S, Chrisman W, Spliethoff B, Tesche B. On the nature of the 'heterogeneous' catalyst: nickel-on-charcoal. The Journal of Organic Chemistry. 68: 1177-89. PMID 12585854 DOI: 10.1021/Jo020296M |
0.768 |
|
| 2003 |
Lipshutz BH, Wood MR, Tirado R. Copper‐Catalyzed Conjugate Addition of Functionalized Organozinc Reagents to α,β‐Unsaturated Ketones: Ethyl 5‐(3‐Oxocyclohexyl)Pentanoate Organic Syntheses. 76: 252-252. DOI: 10.1002/0471264180.Os076.25 |
0.418 |
|
| 2003 |
Lipshutz BH, Moretti R, Crow R. Mixed Higher‐Order Cyanocuprate‐Induced Epoxide Openings: 1‐Benzyloxy‐4‐Penten‐2‐ol Organic Syntheses. 80-80. DOI: 10.1002/0471264180.Os069.10 |
0.362 |
|
| 2002 |
Lipshutz BH, Papa P. Copper-catalyzed reductive alkylations of enones: a novel transmetalation protocol. Angewandte Chemie (International Ed. in English). 41: 4580-2. PMID 12458544 DOI: 10.1002/1521-3773(20021202)41:23<4580::Aid-Anie4580>3.0.Co;2-7 |
0.818 |
|
| 2002 |
Lipshutz BH, Mollard P, Pfeiffer SS, Chrisman W. A short, highly efficient synthesis of coenzyme Q(10). Journal of the American Chemical Society. 124: 14282-3. PMID 12452683 DOI: 10.1021/Ja021015V |
0.787 |
|
| 2002 |
Lipshutz BH, Lower A, Noson K. Copper(I) hydride-catalyzed asymmetric hydrosilylation of heteroaromatic ketones. Organic Letters. 4: 4045-8. PMID 12423082 DOI: 10.1021/Ol026755N |
0.828 |
|
| 2002 |
Bringmann G, Menche D, Mühlbacher J, Reichert M, Saito N, Pfeiffer SS, Lipshutz BH. On the verge of axial chirality: atroposelective synthesis of the AB-biaryl fragment of vancomycin. Organic Letters. 4: 2833-6. PMID 12182567 DOI: 10.1021/Ol026182E |
0.629 |
|
| 2002 |
Hyun MH, Han SC, Lipshutz BH, Shin YJ, Welch CJ. Liquid chromatographic resolution of racemic amines, amino alcohols and related compounds on a chiral crown ether stationary phase. Journal of Chromatography. A. 959: 75-83. PMID 12141563 DOI: 10.1016/S0021-9673(02)00431-4 |
0.537 |
|
| 2002 |
Lipshutz BH, Frieman B, Pfeiffer SS. Heterogeneous catalysis: Ni/C-catalyzed cross-couplings en route to allylated aromatics: Application to a precursor to coenzyme Q10 Synthesis. 2110-2116. DOI: 10.1055/S-2002-34384 |
0.827 |
|
| 2001 |
Lipshutz BH, Pfeiffer SS, Reed AB. Selective cleavage of Cbz-protected amines. Organic Letters. 3: 4145-8. PMID 11784163 DOI: 10.1021/Ol016693L |
0.656 |
|
| 2001 |
Lipshutz BH, Noson K, Chrisman W. Ligand-accelerated, copper-catalyzed asymmetric hydrosilylations of aryl ketones. Journal of the American Chemical Society. 123: 12917-8. PMID 11749557 DOI: 10.1021/Ja011529E |
0.822 |
|
| 2001 |
Lipshutz BH, Blomgren PA. Efficient scavenging of Ph3P and Ph3P=O with high-loading merrifield resin. Organic Letters. 3: 1869-71. PMID 11405732 DOI: 10.1021/ol0159219 |
0.758 |
|
| 2001 |
Hyun MH, Han SC, Lipshutz BH, Shin YJ, Welch CJ. New chiral crown ether stationary phase for the liquid chromatographic resolution of alpha-amino acid enantiomers. Journal of Chromatography. A. 910: 359-65. PMID 11261730 DOI: 10.1016/S0021-9673(00)01230-9 |
0.538 |
|
| 2001 |
Lipshutz BH, Tomioka T, Sato K. Nickel-on-charcoal-catalyzed reductions of aryl chlorides Synlett. 970-973. DOI: 10.1055/S-2001-14636 |
0.683 |
|
| 2001 |
Lipshutz BH, Tomioka T, Pfeiffer SS. Mild and selective reductions of aryl halides catalyzed by low-valent nickel complexes Tetrahedron Letters. 42: 7737-7740. DOI: 10.1016/S0040-4039(01)01522-2 |
0.772 |
|
| 2001 |
Lipshutz BH, Shin YJ. A new silyl linker for reverse-direction solid-phase peptide synthesis Tetrahedron Letters. 42: 5629-5633. DOI: 10.1016/S0040-4039(01)01093-0 |
0.547 |
|
| 2001 |
Lipshutz BH, Chrisman W, Noson K. Hydrosilylation of aldehydes and ketones catalyzed by [Ph3P(CuH)]6 Journal of Organometallic Chemistry. 624: 367-371. DOI: 10.1016/S0022-328X(00)00903-7 |
0.809 |
|
| 2001 |
Lipshutz BH, Tasler S. Preparation of Nickel-on-Charcoal (Ni/C): An Improved Protocol Advanced Synthesis and Catalysis. 343: 327-329. DOI: 10.1002/1615-4169(20010430)343:4<327::Aid-Adsc327>3.0.Co;2-R |
0.336 |
|
| 2001 |
Lipshutz BH. Development of Nickel-on-Charcoal as a ''Dirt-Cheap'' Heterogeneous Catalyst: A Personal Account Advanced Synthesis & Catalysis. 343: 313-326. DOI: 10.1002/1615-4169(20010430)343:4<313::Aid-Adsc313>3.0.Co;2-A |
0.374 |
|
| 2000 |
Lipshutz BH, Shin YJ. Polystyrene-bound cyclo-BINOLs. New heterogeneous ligands for asymmetric catalysis Tetrahedron Letters. 41: 9515-9521. DOI: 10.1016/S0040-4039(00)01660-9 |
0.611 |
|
| 2000 |
Lipshutz BH, Sclafani JA, Blomgren PA. Biaryls via suzuki cross-couplings catalyzed by nickel on charcoal Tetrahedron. 56: 2139-2144. DOI: 10.1016/S0040-4020(99)01096-0 |
0.794 |
|
| 2000 |
Lipshutz BH, Chrisman W, Noson K, Papa P, Sclafani JA, Vivian RW, Keith JM. Copper hydride-catalyzed tandem 1,4-reduction/alkylation reactions Tetrahedron. 56: 2779-2788. DOI: 10.1016/S0040-4020(00)00132-0 |
0.825 |
|
| 1999 |
Lipshutz BH, Keith JM. A Stereospecific, Intermolecular Biaryl-Coupling Approach to Korupensamine A En Route to the Michellamines. Angewandte Chemie (International Ed. in English). 38: 3530-3533. PMID 10602232 DOI: 10.1002/(Sici)1521-3773(19991203)38:23<3530::Aid-Anie3530>3.0.Co;2-W |
0.389 |
|
| 1999 |
Lipshutz BH, Papa P, Keith JM. Triisopropylsilyloxycarbonyl ('Tsoc'): A new protecting group for 1°and 2°amines Journal of Organic Chemistry. 64: 3792-3793. DOI: 10.1021/Jo990272O |
0.791 |
|
| 1999 |
Lipshutz BH, Bulow G, Fernandez-Lazaro F, Kim SK, Lowe R, Mollard P, Stevens KL. A convergent approach to coenzyme Q Journal of the American Chemical Society. 121: 11664-11673. DOI: 10.1021/Ja992164P |
0.349 |
|
| 1999 |
Lipshutz BH, Pfeiffer SS, Chrisman W. Formylations of anions with a 'Weinreb' formamide: N-methoxy-N-methylformamide Tetrahedron Letters. 40: 7889-7892. DOI: 10.1016/S0040-4039(99)01645-7 |
0.769 |
|
| 1999 |
Lipshutz BH, Buzard DJ, Vivian RW. Reductions of aryl perfluorosulfonates with dimethylamine·borane (Me2NH·BH3) catalyzed by Pd(0): An operationally simple, inexpensive, and general protocol Tetrahedron Letters. 40: 6871-6874. DOI: 10.1016/S0040-4039(99)01255-1 |
0.799 |
|
| 1999 |
Lipshutz BH, Müller P, Leinweber D. An intramolecular, Ni(0)-mediated approach to the nonracemic biaryl portion of vancomycin Tetrahedron Letters. 40: 3677-3680. DOI: 10.1016/S0040-4039(99)00557-2 |
0.368 |
|
| 1999 |
Lipshutz BH, Vivian RW. Cu(I)-catalyzed substitution reactions of activated vinyl triflates with functionalized organozinc reagents Tetrahedron Letters. 40: 2871-2874. DOI: 10.1016/S0040-4039(99)00355-X |
0.821 |
|
| 1999 |
Lipshutz BH, Buzard DJ, Yun CS. Pd(0)-mediated couplings of aryl nonaflates and triflates with diphenylphosphine-borane. Preparation of BH3-stabilized, unsymmetrical triarylphosphines Tetrahedron Letters. 40: 201-204. DOI: 10.1016/S0040-4039(98)02334-X |
0.36 |
|
| 1999 |
Lipshutz BH, Blomgren PA, Kim SK. Substitution reactions of aryl chlorides with organozinc reagents catalyzed by Ni(0) Tetrahedron Letters. 40: 197-200. DOI: 10.1016/S0040-4039(98)02271-0 |
0.793 |
|
| 1999 |
Lipshutz BH, Tomioka T, Blomgren PA, Sclafani JA. Kumada couplings catalyzed by nickel on charcoal (Ni/C) Inorganica Chimica Acta. 296: 164-169. DOI: 10.1016/S0020-1693(99)00388-6 |
0.834 |
|
| 1998 |
Lipshutz BH, Ullman B, Lindsley C, Pecchi S, Buzard DJ, Dickson D. A New Bromo Trienyne: Synthesis of all-E, Conjugated Tetra-, Penta-, and Hexaenes Common to Oxo Polyene Macrolide Antibiotics. The Journal of Organic Chemistry. 63: 6092-6093. PMID 11672230 DOI: 10.1021/Jo981107W |
0.489 |
|
| 1998 |
Lipshutz BH, Sclafani JA, Takanami T. Silyl cuprate couplings: Less silicon, accelerated, yet catalytic in copper [4] Journal of the American Chemical Society. 120: 4021-4022. DOI: 10.1021/Ja980152I |
0.388 |
|
| 1998 |
Lipshutz BH, Shin YJ. A modular approach to nonracemic cyclo-BINOLs. Preparation of symmetrically and unsymmetrically substituted ligands Tetrahedron Letters. 39: 7017-7020. DOI: 10.1016/S0040-4039(98)01468-3 |
0.576 |
|
| 1998 |
Lipshutz BH, Keith J, Papa P, Vivian R. A convenient, efficient method for conjugate reductions using catalytic quantities of Cu(I) Tetrahedron Letters. 39: 4627-4630. DOI: 10.1016/S0040-4039(98)00855-7 |
0.799 |
|
| 1998 |
Lipshutz BH, Keith J. Selective deprotection of alkyl vs. aryl silyl ethers Tetrahedron Letters. 39: 2495-2498. DOI: 10.1016/S0040-4039(98)00381-5 |
0.383 |
|
| 1998 |
Lipshutz BH, Kim SK, Mollard P, Blomgren PA, Stevens KL. Nickel(0)-catalyzed couplings of vinyl- alanes and -zirconocenes with chloromethylated heteroaromatics: A route to E-allylated heterocycles Tetrahedron. 54: 6999-7012. DOI: 10.1016/S0040-4020(98)00342-1 |
0.815 |
|
| 1998 |
Lipshutz BH, Kim SK, Mollard P, Stevens KL. An expeditious route to CoQ(n), Vitamins K1 and K2, and related allylated para-quinones utilizing Ni(0) catalysis Tetrahedron. 54: 1241-1253. DOI: 10.1016/S0040-4020(97)10222-8 |
0.578 |
|
| 1997 |
Lipshutz BH, Woo K, Gross T, Buzard DJ, Tirado R. Alkylations of functionalized organozinc reagents with allylic epoxides catalyzed by a cyanocuprate Synlett. 477-478. DOI: 10.1055/S-1997-6130 |
0.419 |
|
| 1997 |
Lipshutz BH, Lindsley C. A streamlined route to highly conjugated, all-E polyenes characteristic of oxo polyene macrolide antibiotics Journal of the American Chemical Society. 119: 4555-4556. DOI: 10.1021/Ja963930K |
0.517 |
|
| 1997 |
Lipshutz BH. Downsizing Copper in Modern Cuprate Couplings Accounts of Chemical Research. 30: 277-282. DOI: 10.1021/Ar960297Z |
0.366 |
|
| 1997 |
Lipshutz BH, Mollard P, Lindsley C, Chang V. Cyclo-SEM: A new carbonyl protecting group Tetrahedron Letters. 38: 1873-1876. DOI: 10.1016/S0040-4039(97)00239-6 |
0.664 |
|
| 1997 |
Lipshutz BH, James B, Vance S, Cairico I. A potentially general intramolecular biaryl coupling approach to optically pure 2,2'-BINOL analogs Tetrahedron Letters. 38: 753-756. DOI: 10.1016/S0040-4039(96)02453-7 |
0.42 |
|
| 1997 |
Lipshutz BH, Gross T, Buzard DJ, Tirado R. Cuprate-catalyzed Three-Component Couplings of Functionalized Organozinc Reagents Journal of the Chinese Chemical Society. 44: 1-4. DOI: 10.1002/Jccs.199700001 |
0.357 |
|
| 1996 |
Lipshutz BH, Aue DH, James B. An ab initio molecular orbital study on the Lewis acidity of TMS-Cl and TMS-CN toward an α,β-unsaturated aldehyde: Are these acid-base interactions important in organocuprate 1,4-additions to enones? Tetrahedron Letters. 37: 8471-8474. DOI: 10.1016/0040-4039(96)01969-7 |
0.307 |
|
| 1996 |
Lipshutz BH, Bülow G, Lowe RF, Stevens KL. Allylated aromatics via Ni-catalyzed couplings of benzylic chlorides and vinylic organometallics Tetrahedron. 52: 7265-7276. DOI: 10.1016/0040-4020(96)00250-5 |
0.49 |
|
| 1995 |
Lipshutz BH, Gross T. (2,4,6-triisopropylphenyl)selenium bromide (TIPPSe-Br). An in situ-generated reagent for effecting highly selective ring closures of homoallylic alcohols to substituted tetrahydrofurans Journal of Organic Chemistry. 60: 3572-3573. DOI: 10.1021/Jo00117A001 |
0.304 |
|
| 1995 |
Lipshutz BH, Wood MR, Tirado R. Michael additions of functionalized organozinc reagents mediated by catalytic quantities of copper(I) Journal of the American Chemical Society. 117: 6126-6127. DOI: 10.1021/Ja00127A028 |
0.382 |
|
| 1995 |
Lipshutz BH, Wood MR, Lindsley CW. Spectroscopic experiments on the role of Me3SiCl in lithium dialkylamide deprotonations Tetrahedron Letters. 36: 4385-4388. DOI: 10.1016/0040-4039(95)00856-8 |
0.483 |
|
| 1995 |
Lipshutz BH, Segi M. Catalytic Cu(I) assisted polyfunctionalization of zirconacyclopentenes Tetrahedron. 51: 4407-4420. DOI: 10.1016/0040-4020(94)01129-N |
0.409 |
|
| 1994 |
Lipshutz BH, Bhandari A, Lindsley C, Keil R, Wood MR. New synthetic methods based on organozirconium and organocopper chemistry Pure and Applied Chemistry. 66: 1493-1500. DOI: 10.1351/Pac199466071493 |
0.464 |
|
| 1994 |
Lipshutz BH, Hayakawa H, Kato K, Lowe RF, Stevens KL. A novel route to pyrimidine nucleosides via intramolecular couplings of bases with 2'-deoxyribosides: Quick and stereospecific...but with a 'twist' Synthesis. 1476-1484. DOI: 10.1055/S-1994-25717 |
0.365 |
|
| 1994 |
Lipshutz BH, Tirado R. De Novo Approach To Dideoxyribosides. 5-Endo-Trig-Like Cyclizations Of Delta -Hydroxy Enol Ethers Journal of Organic Chemistry. 59: 8307-8311. DOI: 10.1021/Jo00105A067 |
0.323 |
|
| 1994 |
Lipshutz BH, James B. New 1H and 13C NMR spectral data on "higher order" cyanocuprates. If the cyano ligand is not on copper, then where is it? Journal of Organic Chemistry. 59: 7585-7587. DOI: 10.1021/Jo00104A009 |
0.301 |
|
| 1994 |
Lipshutz BH, Hackmann C. Conjugate addition reactions of allylic copper species derived from grignard reagents: Synthetic and spectroscopic aspects Journal of Organic Chemistry. 59: 7437-7444. DOI: 10.1021/Jo00103A042 |
0.424 |
|
| 1994 |
Lipshutz BH, Wood MR. Spectroscopic studies on cyanocuprate-catalyzed 3-component couplings: understanding the catalytic cycle Tetrahedron Letters. 35: 6433-6436. DOI: 10.1016/S0040-4039(00)78239-6 |
0.479 |
|
| 1994 |
Lipshutz BH, Liu ZP, Kayser F. Cyanocuprate-mediated intramolecular biaryl couplings applied to an ellagitannin. Synthesis of (+)-O-permethyltellimagrandin II Tetrahedron Letters. 35: 5567-5570. DOI: 10.1016/S0040-4039(00)77248-0 |
0.32 |
|
| 1994 |
Lipshutz BH, Lindsley C, Bhandari A. Expanding the versatility of Schwartz' reagent: Hydrozirconation of vinylic and acetylenic acyl silanes Tetrahedron Letters. 35: 4669-4672. DOI: 10.1016/S0040-4039(00)76937-1 |
0.531 |
|
| 1994 |
Lipshutz BH, Kayser F, Maullin N. Inter- and intramolecular biaryl couplings via cyanocuprate intermediates Tetrahedron Letters. 35: 815-818. DOI: 10.1016/S0040-4039(00)75970-3 |
0.377 |
|
| 1994 |
Lipshutz BH, Lindsley C, Susfalk R, Gross T. A convenient preparation of triisopropylsilyl acyl silanes Tetrahedron Letters. 35: 8999-9002. DOI: 10.1016/0040-4039(94)88410-2 |
0.463 |
|
| 1994 |
Lipshutz BH, Keil R. Hydrozirconation/transmetalation of acetylenic stannanes. New 1,1-dimetallo reagents Inorganica Chimica Acta. 220: 41-44. DOI: 10.1016/0020-1693(94)03852-X |
0.393 |
|
| 1994 |
Lipshutz BH, Kayser F, Liu ZP. Asymmetric synthesis of biaryls by intramolecular oxidative couplings of cyanocuprate intermediates Angewandte Chemie (International Edition in English). 33: 1842-1844. DOI: 10.1002/Anie.199418421 |
0.384 |
|
| 1993 |
Lipshutz BH, Alami M, Susfalk RB. Stannylated Enynes as Linchpins for Pd-Catalyzed Couplings with Unactivated Vinyl Iodides Synlett. 1993: 693-695. DOI: 10.1055/S-1993-22575 |
0.349 |
|
| 1993 |
Lipshutz BH, Wood MR. Cyanocuprate-catalyzed 1,4-additions of vinylic zirconocenes using a zincate as an organolithium shuttle. A new and potentially practical approach to 3-component couplings Journal of the American Chemical Society. 115: 12625-12626. DOI: 10.1021/Ja00079A068 |
0.34 |
|
| 1993 |
Lipshutz BH, Dimock SH, James B. The role of trimethylsilyl chloride in Gilman cuprate 1,4-addition reactions Journal of the American Chemical Society. 115: 9283-9284. DOI: 10.1021/Ja00073A052 |
0.382 |
|
| 1993 |
Lipshutz BH, Siegmann K, Garcia E, Kayser F. Synthesis of unsymmetrical biaryls via kinetic higher order cyanocuprates: scope, limitations, and spectroscopic insights Journal of the American Chemical Society. 115: 9276-9282. DOI: 10.1021/Ja00073A051 |
0.339 |
|
| 1993 |
Lipshutz BH, Kayser F, Siegmann K. Some observations on the solution composition of Gilman reagent (“R2CuLi”) Tetrahedron Letters. 34: 6693-6696. DOI: 10.1016/S0040-4039(00)61677-5 |
0.385 |
|
| 1993 |
Lipshutz BH, Alami M. Polyene constructions via palladium couplings of activated triflates with stannylated enynes Tetrahedron Letters. 34: 1433-1436. DOI: 10.1016/S0040-4039(00)60311-8 |
0.416 |
|
| 1992 |
Lipshutz BH, Sharma S, Dimock SH, Behling JR. Preparation of C-4 Alkylated Dideoxyribosides: Potential Precursors to a Novel Series of Nucleosides Synthesis. 1992: 191-195. DOI: 10.1055/S-1992-34158 |
0.369 |
|
| 1992 |
Lipshutz BH, Keil R. Preparation and use of vinylic lithiocyanocuprates containing an .omega.-electrophilic center Journal of the American Chemical Society. 114: 7919-7920. DOI: 10.1021/Ja00046A052 |
0.313 |
|
| 1992 |
Lipshutz BH, Barton JC. Reagent-based stereocontrol in formation of substituted tetrahydrofurans Journal of the American Chemical Society. 114: 1084-1086. DOI: 10.1021/Ja00029A045 |
0.331 |
|
| 1992 |
Wasserman HH, Ching TY, Lipshutz BH, Matsuyama H, Scully FE, Wang P. Synthesis and kinetic studies of a novel singlet oxygen donor with acceptor-binding capability Bioorganic & Medicinal Chemistry Letters. 2: 1137-1140. DOI: 10.1016/S0960-894X(00)80634-4 |
0.5 |
|
| 1992 |
Lipshutz BH, Keil R, Barton JC. Preparation of Z-vinylstannanes via hydrozirconation of stannylacetylenes Tetrahedron Letters. 33: 5861-5864. DOI: 10.1016/S0040-4039(00)61073-0 |
0.331 |
|
| 1992 |
Venanzi LM, Lehmann R, Keil R, Lipshutz BH. Copper-catalyzed allylic alkylations of alkylzirconium intermediates Tetrahedron Letters. 33: 5857-5860. DOI: 10.1016/S0040-4039(00)61072-9 |
0.43 |
|
| 1992 |
Lipshutz BH, Seigmann K, Garcia E. Controlled ‘decomposition’ of “kinetic” higher order cyanocuprates: A new route to unsymmetrical biaryls Tetrahedron. 48: 2579-2588. DOI: 10.1016/S0040-4020(01)88522-7 |
0.36 |
|
| 1992 |
Arai M, Lipshutz BH, Nakamura E. Copper-catalyzed reactions of organotitanium reagents. Highly selective SN2′-allylation and conjugate addition Tetrahedron. 48: 5709-5718. DOI: 10.1016/0040-4020(92)80022-8 |
0.448 |
|
| 1991 |
Lipshutz BH, Dimock SH. Carboalumination/transmetalation/conjugate addition: a new catalytic copper(I)-induced process for the 1,4-delivery of vinylic groups to enones Journal of Organic Chemistry. 56: 5761-5763. DOI: 10.1021/Jo00020A012 |
0.34 |
|
| 1991 |
Arai M, Nakamura E, Lipshutz BH. Copper-catalyzed reactions of organotitanium reagents. Highly SN2'- and anti-selective and diastereo- and chemoselective alkylation of allylic chlorides and phosphates The Journal of Organic Chemistry. 56: 5489-5491. DOI: 10.1021/Jo00019A001 |
0.446 |
|
| 1991 |
Lipshutz BH, Kato K. Hydrozirconation / transmetalation / alkylation: direct one-pot conversion of 1-alkynes to E-1,2-disubstituted alkenes Tetrahedron Letters. 32: 5647-5650. DOI: 10.1016/S0040-4039(00)93519-6 |
0.406 |
|
| 1990 |
Lipshutz BH, Elworthy TR. Intermolecular couplings between vinyl triflates and allylic cuprates: a mild and rapid atypical route to 1,4-dienes Journal of Organic Chemistry. 55: 1695-1696. DOI: 10.1021/Jo00293A002 |
0.423 |
|
| 1990 |
Lipshutz BH, Huff BE, McCarthy KE, Mukarram SMJ, Siahaan TJ, Vaccaro WD, Webb H, Falick AM, Miller TA. Oxazolophanes as masked cyclopeptide alkaloid equivalents: cyclic peptide chemistry without peptide couplings Journal of the American Chemical Society. 112: 7032-7041. DOI: 10.1021/Ja00175A039 |
0.553 |
|
| 1990 |
Lipshutz BH, Ellsworth EL, Dimock SH, Smith RAJ. New methodology for conjugate additions of allylic ligands to .alpha.,.beta.-unsaturated ketones: synthetic and spectroscopic studies Journal of the American Chemical Society. 112: 4404-4410. DOI: 10.1021/Ja00167A043 |
0.32 |
|
| 1990 |
Lipshutz BH, Crow R, Dimock SH, Ellsworth EL, Smith RAJ, Behling JR. Ligand exchange between cyanocuprates and allylic stannanes: a novel, direct route to allylic cuprates possessing remarkable reactivity and stability Journal of the American Chemical Society. 112: 4063-4064. DOI: 10.1021/Ja00166A067 |
0.355 |
|
| 1990 |
Lipshutz BH, Miller TA. The stereochemical outcome from mitsunobu couplings of vicinal, N-protected acyclic amino alcohols Tetrahedron Letters. 31: 5253-5256. DOI: 10.1016/S0040-4039(00)98043-2 |
0.338 |
|
| 1990 |
Lipshutz BH, Ung C, Elworthy TR, Reuter DC. Preparation and reactions of cyclic allylic higher order cyanocuprates Tetrahedron Letters. 31: 4539-4542. DOI: 10.1016/S0040-4039(00)97669-X |
0.43 |
|
| 1990 |
Lipshutz BH, Keil R, EIIsworth EL. A new method for the in situ generation of Cp2Zr(H)Cl (Schwartz' Reagent) Tetrahedron Letters. 31: 7257-7260. DOI: 10.1016/S0040-4039(00)88538-X |
0.302 |
|
| 1990 |
Lipshutz BH, Sharma S, Reuter DC. A new transmetallation route to mixed trimethylstannylcuprates: Me3Sn(r)Cu(CN)Li2 Tetrahedron Letters. 31: 7253-7256. DOI: 10.1016/S0040-4039(00)88537-8 |
0.307 |
|
| 1990 |
Lipshutz BH, Elworthy TR. 1,4-Acylation reactions by allylic cuprates in the presence of carbon monoxide Tetrahedron Letters. 31: 477-480. DOI: 10.1016/0040-4039(90)87012-O |
0.37 |
|
| 1989 |
Lipshutz BH, Ellsworth EL, Siahaan TJ. The Role of BF3·Et2O in Reactions of Lower Order (Gilman) Organocuprates Journal of the American Chemical Society. 111: 1351-1358. DOI: 10.1021/Ja00186A031 |
0.574 |
|
| 1989 |
Lipshutz BH, Ellsworth EL, Dimock SH, Reuter DC. Transmetalation reactions of higher order cyanocuprates: Direct formation of trialkyltin cuprates from tin hydrides which bypasses organolithium intermediates Tetrahedron Letters. 30: 2065-2068. DOI: 10.1016/S0040-4039(01)93712-8 |
0.378 |
|
| 1989 |
Lipshutz BH, Reuter DC. Convenient preparation and manipulation of Me3SnH from Me3SnCl. Formation and use of mixed trimethylstannylcuprates via transmetalation reactions Tetrahedron Letters. 30: 4617-4620. DOI: 10.1016/S0040-4039(01)80757-7 |
0.346 |
|
| 1989 |
Behling JR, Ng JS, Babiak KA, Campbell AL, Elsworth E, Lipshutz BH. The synthesis of β-Hydroxy-(E)-vinylstannanes using an "in-situ" generated cuprate reagent derived from (E)-bis-(tributylstannyl)ethylene Tetrahedron Letters. 30: 27-30. DOI: 10.1016/S0040-4039(01)80313-0 |
0.314 |
|
| 1989 |
Lipshutz BH, Moretti R, Crow R. Progress toward roflamycoin; Synthesis of the C-12 to C-35 section in homochiral form Tetrahedron Letters. 30: 15-18. DOI: 10.1016/S0040-4039(01)80310-5 |
0.329 |
|
| 1988 |
Lipshutz BH, Ellsworth EL, Siahaan TJ. Effects of BF3•Et2O on higher order organocuprate reactions: substrate activation or cuprate modification Journal of the American Chemical Society. 110: 4834-4835. DOI: 10.1021/Ja00222A055 |
0.582 |
|
| 1988 |
Lipshutz BH, Ellsworth EL, Behling JR, Campbell AL. Effects of gengenions on organocuprate reactivity/selectivity: Higher order, mixed lithio-sodio cyanocuprates Tetrahedron Letters. 29: 893-896. DOI: 10.1016/S0040-4039(00)82475-2 |
0.321 |
|
| 1988 |
Lipshutz BH, Ellsworth EL, Siahaan TJ, Shirazi A. Unexpected affects of Me3Si-X on reactions of higher order cyanocuprates Tetrahedron Letters. 29: 6677-6680. DOI: 10.1016/S0040-4039(00)82426-0 |
0.521 |
|
| 1988 |
Lipshutz BH, Reuter DC. Cyclopeptide alkaloid model studies. A two-step conversion of 5-aminoisoxazoles to amino acid bis-amides Tetrahedron Letters. 29: 6067-6070. DOI: 10.1016/S0040-4039(00)82266-2 |
0.336 |
|
| 1988 |
Lipshutz BH, Nguyen SL, Elworthy TR. Preparation and diels-alder reactions of a pyranoid vinyl glycal:model studies for anthraquinone aglycone and carbohydrate syntheses Tetrahedron. 44: 3355-3364. DOI: 10.1016/S0040-4020(01)85970-6 |
0.401 |
|
| 1988 |
Ng JS, Behling JR, Campbell AL, Nguyen D, Lipshutz B. Reactions of higher order cyanocuprates derived from 2-lithiated furans: scope, limitations, and synthetic utility Tetrahedron Letters. 29: 3045-3048. DOI: 10.1016/0040-4039(88)85081-0 |
0.385 |
|
| 1986 |
Lipshutz BH. Five-membered heteroaromatic rings as intermediates in organic synthesis Chemical Reviews. 86: 795-819. DOI: 10.1021/Cr00075A005 |
0.312 |
|
| 1986 |
Lipshutz BH, Huff B, Vaccaro W. Preparation of (±)-α-alkylated amino acid derivatives via imidazoles Tetrahedron Letters. 27: 4241-4244. DOI: 10.1016/S0040-4039(00)94242-4 |
0.318 |
|
| 1986 |
Lipshutz BH, Kotsuki H, Lew W. Es route to polyene macrolide total synthesis; The key chiral segments of roflamycoin Tetrahedron Letters. 27: 4825-4828. DOI: 10.1016/S0040-4039(00)85073-X |
0.323 |
|
| 1986 |
Lipshutz BH, Vaccaro W, Huff B. Protection of imidazoles as their β-trimethylsilylethoxymethyl (SEM) derivatives Tetrahedron Letters. 27: 4095-4098. DOI: 10.1016/S0040-4039(00)84919-9 |
0.326 |
|
| 1986 |
Lipshutz BH, Parker DA, Nguyen SL, McCarthy KE, Barton JC, Whitney SE, Kotsuki H. Reactions of stoichiometric higher order, mixed lithio magnesio organocuprates Tetrahedron. 42: 2873-2879. DOI: 10.1016/S0040-4020(01)90576-9 |
0.415 |
|
| 1986 |
Lipshutz BH, Hungate RW, Mccarthy KE. Chiral Induction in Originally Racemic Amino Acids via 5‐Acyl and 5‐Acyloxyaminooxazoles Israel Journal of Chemistry. 27: 49-55. DOI: 10.1002/Ijch.198600009 |
0.335 |
|
| 1985 |
Lipshutz BH, Kozlowski JA, Breneman CM. Chemical and spectroscopic studies on copper iodide derived organocuprates: new insight into the composition of Gilman's reagent Journal of the American Chemical Society. 107: 3197-3204. DOI: 10.1021/Ja00297A027 |
0.302 |
|
| 1985 |
Lipshutz BH, Pollart D, Monforte J, Kotsuki H. Pd(II)-catalyzed acetal/ketal hydrolysis/exchange reactions Tetrahedron Letters. 26: 705-708. DOI: 10.1016/S0040-4039(00)89114-5 |
0.42 |
|
| 1985 |
Lipshutz BH, Kozlowski JA, Parker DA, Nguyen SL, McCarthy KE. More highly mixed, higher order cyanocuprates "RT(2-thienyl)Cu(CN)Li2". Efficient reagents which promote selective ligand transfer Journal of Organometallic Chemistry. 285: 437-447. DOI: 10.1016/0022-328X(85)87388-5 |
0.383 |
|
| 1985 |
LIPSHUTZ BH, KOZLOWSKI JA, BRENEMAN CM. ChemInform Abstract: CHEMICAL AND SPECTROSCOPIC STUDIES ON COPPER IODIDE DERIVED ORGANOCUPRATES: NEW INSIGHT INTO THE COMPOSITION OF GILMAN′S REAGENT Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198538300 |
0.321 |
|
| 1985 |
Lipshutz BH, Pollart D, Monforte J, Kotsuki H. Palladium(Ii)-Catalyzed Acetal/Ketal Hydrolysis/Exchange Reactions Cheminform. 16. DOI: 10.1002/Chin.198525092 |
0.407 |
|
| 1985 |
LIPSHUTZ BH, WILHELM RS, KOZLOWSKI JA. ChemInform Abstract: CONJUGATE ADDITION REACTIONS OF α,β-UNSATURATED KETONES WITH HIGHER ORDER, MIXED ORGANOCUPRATE REAGENTS, R2CU(CN)LI2 Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198515121 |
0.341 |
|
| 1984 |
Lipshutz BH, Wilhelm RS, Kozlowski JA. Conjugate addition reactions of .alpha.,.beta.-unsaturated ketones with higher order, mixed organocuprate reagents, R2Cu(CN)Li2 The Journal of Organic Chemistry. 49: 3938-3942. DOI: 10.1021/Jo00195A010 |
0.326 |
|
| 1984 |
Lipshutz BH, Parker DA, Kozlowski JA, Nguyen SL. Effects of Lewis acids on higher order, mixed cuprate couplings Tetrahedron Letters. 25: 5959-5962. DOI: 10.1016/S0040-4039(01)81732-9 |
0.416 |
|
| 1984 |
Lipshutz BH, Wilhelm RS, Kozlowski JA, Parker D. Substitution reactions of secondary halides and epoxides with higher order, mixed organocuprates, R2Cu(CN)Li2: synthetic, stereochemical, and mechanistic aspects The Journal of Organic Chemistry. 49: 3928-3938. DOI: 10.1002/Chin.198515119 |
0.394 |
|
| 1984 |
Lipshutz BH, Kozlowski JA. A reiterative route to chiral all-syn-1,3-polyols The Journal of Organic Chemistry. 49: 1147-1149. DOI: 10.1002/Chin.198434080 |
0.305 |
|
| 1984 |
Lipshutz BH, Morey MC. Heterocycles in synthesis: chiral amino acids/dipeptides via a novel photooxidative cleavage of trisubstituted imidazoles Cheminform. 15. DOI: 10.1002/Chin.198417348 |
0.327 |
|
| 1984 |
Lipshutz BH, Hungate RW, Mccarthy KE. Heterocycles As Masked Diamide/Dipeptide Equivalents. Formation And Reactions Of Substituted 5-(Acylamino)Oxazoles As Intermediates En Route To The Cyclopeptide Alkaloids Cheminform. 15. DOI: 10.1002/Chin.198414206 |
0.415 |
|
| 1984 |
Lipshutz BH, Morey MC. An Approach To The Cyclopeptide Alkaloids (Phencyclopeptines) Via Heterocyclic Diamide/Dipeptide Equivalents. Preparation And N-Alkylation Studies Of 2,4(5)-Disubstituted Imidazoles Cheminform. 15. DOI: 10.1002/Chin.198411196 |
0.304 |
|
| 1984 |
Lipshutz BH, Parker D, Kozlowski JA, Miller RD. Coupling Reactions Of Higher Order Cuprates With Primary Halides: Extremely Mild And Efficient Substitution Reactions Of Bromides And Chlorides Cheminform. 15. DOI: 10.1002/Chin.198407080 |
0.445 |
|
| 1984 |
LIPSHUTZ BH, WILHELM RS, NUGENT ST, LITTLE RD, BAIZER MM. ChemInform Abstract: ELECTROCHEMICAL PEAK POTENTIALS OF TYPICAL SUBSTRATES USED FOR COUPLING REACTIONS WITH ORGANOCUPRATES: EFFECTS OF SOLVENT Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198407074 |
0.301 |
|
| 1983 |
Lipshutz BH, Morey MC. An approach to the cyclopeptide alkaloids (phencyclopeptines) via heterocyclic diamide/dipeptide equivalents. Preparation and N-alkylation studies of 2,4(5)-disubstituted imidazoles Journal of Organic Chemistry. 48: 3745-3750. DOI: 10.1021/Jo00169A027 |
0.304 |
|
| 1983 |
Lipshutz BH, Parker D, Kozlowski JA, Miller RD. Coupling reactions of higher order cuprates with primary halides: extremely mild and efficient substitution reactions of bromides and chlorides Journal of Organic Chemistry. 48: 3334-3336. DOI: 10.1021/Jo00167A037 |
0.445 |
|
| 1983 |
Lipshutz BH, Kozlowski JA, Wilhelm RS. Chemistry of higher order, mixed organocuprates. 5. On the choice of the copper(I) salt for the formation of R2CuLi The Journal of Organic Chemistry. 48: 546-550. DOI: 10.1021/Jo00152A026 |
0.303 |
|
| 1983 |
Lipshutz BH, Hungate RW, McCarthy KE. Heterocycles as masked diamide/dipeptide equivalents. Formation and reactions of substituted 5-(acylamino)oxazoles as intermediates en route to the cyclopeptide alkaloids Journal of the American Chemical Society. 105: 7703-7713. DOI: 10.1021/Ja00364A041 |
0.301 |
|
| 1983 |
Lipshutz BH, Hungate RW, McCarthy KE. Heterocycles in synthesis, dipeptides via unmasking of 5-acyl- and 5-acyloxyaminooxazoles Tetrahedron Letters. 24: 5155-5158. DOI: 10.1016/S0040-4039(00)88384-7 |
0.383 |
|
| 1983 |
Lipshutz BH. Conjugate addition reactions of α,β- unsaturated esters with higher order cuprates R2 Cu(CN)Li2 Tetrahedron Letters. 24: 127-130. DOI: 10.1016/S0040-4039(00)81346-5 |
0.312 |
|
| 1983 |
Lipshutz BH, Wilhelm RS, Nugent ST, Little RD, Baizer MM. Electrochemical peak potentials of typical substrates used for coupling reactions with organocuprates: effects of solvent The Journal of Organic Chemistry. 48: 3306-3308. DOI: 10.1002/Chin.198407074 |
0.406 |
|
| 1982 |
Lipshutz BH, Harvey DF. Hydrolysis of Acetals and Ketals Using LiBF4 Synthetic Communications. 12: 267-277. DOI: 10.1080/00397918209409233 |
0.319 |
|
| 1982 |
Lipshutz BH, Wilhelm RS. Chemistry of higher order, mixed organocuprates. 4. The stereochemical outcome of substitution reactions at unactivated secondary centers using organocopper reagents Journal of the American Chemical Society. 104: 4696-4698. DOI: 10.1021/Ja00381A041 |
0.349 |
|
| 1982 |
Lipshutz BH, Kozlowski J, Wilhelm RS. Chemistry of higher order mixed organocuprates. 2. Reactions of epoxides Journal of the American Chemical Society. 104: 2305-2307. DOI: 10.1021/Ja00372A032 |
0.358 |
|
| 1982 |
Lipshutz BH, Wilhelm RS, Kozlowski J. Chemistry of higher order, mixed organocuprates. reactions of α,β-unsaturated ketones Tetrahedron Letters. 23: 3755-3758. DOI: 10.1016/S0040-4039(00)87698-4 |
0.353 |
|
| 1981 |
Wasserman HH, Lipshutz BH, Tremper AW, Wu JS. Preparation of .beta.-lactams from azetidine-2-carboxylic acids and esters Journal of Organic Chemistry. 12: 2991-2999. DOI: 10.1021/Jo00328A001 |
0.496 |
|
| 1981 |
Lipshutz BH, Wilhelm RS, Floyd DM. Chemistry of higher order, mixed organocuprates. 1. Substitution reactions at unactivated secondary centers Journal of the American Chemical Society. 103: 7672-7674. DOI: 10.1021/Ja00415A055 |
0.378 |
|
| 1980 |
Lipshutz BH, Pegram JJ. β-(Trimethylsilyl)ethoxymethyl chloride. A new reagent for the protection of the hydroxyl group Tetrahedron Letters. 21: 3343-3346. DOI: 10.1016/S0040-4039(00)78684-9 |
0.361 |
|
| 1980 |
WASSERMAN HH, LIPSHUTZ BH. ChemInform Abstract: REACTIONS OF SINGLET OXYGEN WITH HETEROCYCLIC SYSTEMS Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198020311 |
0.535 |
|
| 1978 |
Corey EJ, Floyd D, Lipshutz BH. (3-Methyl-3-methoxy-1-butynyl)copper, a useful reagent for the generation of mixed cuprates Journal of Organic Chemistry. 43: 3418-3420. DOI: 10.1021/Jo00411A045 |
0.43 |
|
| 1977 |
Wasserman HH, Lipshutz BH, Wu JS. Enamine-singlet Oxygen Reactions. Synthesis of b-Lactams from Esters of Azatidine Carboxylic Acids Cheminform. 7: 321. DOI: 10.1002/Chin.197813173 |
0.565 |
|
| 1976 |
Wasserman HH, Lipshutz BH. A new synthesis of β-lactams. oxygenation of dianions Of azetidine carboxylic acids Tetrahedron Letters. 17: 4613-4616. DOI: 10.1016/S0040-4039(00)93945-5 |
0.504 |
|
| 1975 |
Wasserman HH, Lipshutz BH. Oxidative decarboxylation of acids via dianion oxygenation Tetrahedron Letters. 16: 4611-4614. DOI: 10.1016/S0040-4039(00)91083-9 |
0.46 |
|
| 1975 |
Wasserman HH, Lipshutz BH. Reactions of lithium enolates with molecular oxygen α-hydroxylation of amides and other carboxylate derivatives Tetrahedron Letters. 16: 1731-1734. DOI: 10.1016/S0040-4039(00)72245-3 |
0.554 |
|
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