| Year |
Citation |
Score |
| 2023 |
Hernandez JJ, Lawrie AP, Frontier AJ. Alkynyl Halo-Aza-Prins Annulative Couplings. The Journal of Organic Chemistry. PMID 37971946 DOI: 10.1021/acs.joc.3c01305 |
0.363 |
|
| 2023 |
Milosavljevic A, Holt C, Frontier AJ. Nitrogen-interrupted -Prins/-Nazarov fragment coupling cascade for the synthesis of indolines. Chemical Science. 14: 5431-5437. PMID 37234889 DOI: 10.1039/d3sc00986f |
0.428 |
|
| 2022 |
Hernandez JJ, Frontier AJ. Alkynyl Prins carbocyclization cascades for the synthesis of linear-fused heterocyclic ring systems. Chemical Science. 13: 13836-13842. PMID 36544720 DOI: 10.1039/d2sc04750k |
0.824 |
|
| 2022 |
Thoenen M, Gettings M, Holt C, Frontier AJ, Caruana PA, Zeller M, Byrd EFC, Piercey DG. Approach to High-Nitrogen Materials with Dual-Use Properties via Tetraaza-Nazarov Cyclization. Inorganic Chemistry. PMID 36318095 DOI: 10.1021/acs.inorgchem.2c02649 |
0.823 |
|
| 2022 |
Yadykov AV, Eremchenko AE, Milosavljevic A, Frontier AJ, Shirinian VZ. Divergent Reactivity of Triaryldivinyl Ketones: Competing 4π and Putative 6π Electrocyclization Pathways. The Journal of Organic Chemistry. 87: 13643-13652. PMID 36220664 DOI: 10.1021/acs.joc.2c01294 |
0.796 |
|
| 2021 |
Frontier AJ, Sinclair PP. Merging Strategy, Improvisation, and Conversation to Solve Problems in Target Synthesis. Accounts of Chemical Research. PMID 33705115 DOI: 10.1021/acs.accounts.0c00804 |
0.301 |
|
| 2021 |
Hernandez JJ, Frontier AJ. Synthesis of Spirocyclic Isoindolones Using an Alkynyl -Prins/Oxidative -Nazarov Cyclization Sequence. Organic Letters. PMID 33591209 DOI: 10.1021/acs.orglett.1c00191 |
0.824 |
|
| 2020 |
Frontier AJ, Hernandez JJ. New Twists in Nazarov Cyclization Chemistry. Accounts of Chemical Research. PMID 32790284 DOI: 10.1021/Acs.Accounts.0C00284 |
0.815 |
|
| 2020 |
Alachouzos G, Holt C, Frontier AJ. Correction to "Stereochemical Relay through a Cationic Intermediate: Helical Preorganization Dictates Direction of Conrotation in the -Nazarov Cyclization". Organic Letters. 22: 5713. PMID 32633967 DOI: 10.1021/Acs.Orglett.0C02062 |
0.398 |
|
| 2020 |
Abdul-Rashed S, Alachouzos G, Brennessel WW, Frontier AJ. Correction to "One-Pot Double-Annulation Strategy for the Synthesis of Unusual Fused Bis-Heterocycles". Organic Letters. PMID 32598846 DOI: 10.1021/Acs.Orglett.0C01958 |
0.48 |
|
| 2020 |
Abdul-Rashed S, Alachouzos G, Brennessel WW, Frontier AJ. One-Pot Double-Annulation Strategy for the Synthesis of Unusual Fused Bis-Heterocycles. Organic Letters. PMID 32412769 DOI: 10.1021/Acs.Orglett.0C01351 |
0.483 |
|
| 2020 |
Alachouzos G, Holt C, Frontier AJ. Stereochemical Relay through a Cationic Intermediate: Helical Preorganization Dictates Direction of Conrotation in the -Nazarov Cyclization. Organic Letters. PMID 32352794 DOI: 10.1021/acs.orglett.0c01330 |
0.357 |
|
| 2020 |
Abdul-Rashed S, Holt C, Frontier AJ. Alkynyl Prins and Alkynyl Aza-Prins Annulations: Scope and Synthetic Applications Synthesis. 52: 1991-2007. DOI: 10.1055/S-0039-1690869 |
0.589 |
|
| 2019 |
Holt C, Alachouzos G, Frontier AJ. Leveraging the Halo-Nazarov Cyclization for the Chemodivergent Assembly of Functionalized Haloindenes and Indanones. Journal of the American Chemical Society. PMID 30900884 DOI: 10.1021/Jacs.9B00198 |
0.491 |
|
| 2019 |
Parsons DE, Frontier AJ. Noncanonical Cation-π Cyclizations of Alkylidene β-Ketoesters: Synthesis of Spiro-fused and Bridged Bicyclic Ring Systems. Organic Letters. PMID 30869901 DOI: 10.1021/Acs.Orglett.9B00094 |
0.499 |
|
| 2018 |
Alachouzos G, Frontier AJ. Cationic Cascade for Building Complex Polycyclic Molecules from Simple Precursors: Diastereoselective Installation of Three Contiguous Stereogenic Centers in a One-Pot Process. Journal of the American Chemical Society. PMID 30571090 DOI: 10.1021/Jacs.8B11713 |
0.434 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/S-0036-1591747 |
0.833 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2018 |
Frontier A, Carlsen P, Stoutenburg E. SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation Synthesis. 50: 1238-1245. DOI: 10.1055/s-0036-1591747 |
0.416 |
|
| 2017 |
Alachouzos G, Frontier AJ. Diastereoselective Construction of Densely Functionalized 1-Halocyclopentenes Using an Alkynyl Halo-Prins/Halo-Nazarov Cyclization Strategy. Angewandte Chemie (International Ed. in English). PMID 29065241 DOI: 10.1002/Anie.201709482 |
0.451 |
|
| 2016 |
Huang YW, Frontier AJ. Nazarov Cyclization/Internal Redox Cyclization Sequence for the Synthesis of N-Heterocyclic Bridged Ring Systems. Organic Letters. PMID 27652822 DOI: 10.1021/Acs.Orglett.6B02369 |
0.525 |
|
| 2015 |
Carlsen P, Jiang C, Herrick IR, Frontier AJ. Studies toward the AB ring system of the tetrapetalone natural products. Tetrahedron. 71: 5886-5896. PMID 26309334 DOI: 10.1016/J.Tet.2015.05.021 |
0.806 |
|
| 2015 |
Huang YW, Frontier AJ. Enantioselective Nazarov Cyclization Catalyzed by a Cinchona Alkaloid Derivative. Tetrahedron Letters. 56: 3523-3526. PMID 26085696 DOI: 10.1016/J.Tetlet.2014.12.136 |
0.496 |
|
| 2015 |
Carlsen PN, Jiang C, Herrick IR, Frontier AJ. Studies toward the AB ring system of the tetrapetalone natural products Tetrahedron. DOI: 10.1016/j.tet.2015.05.021 |
0.776 |
|
| 2014 |
Jacob SD, Brooks JL, Frontier AJ. No acid required: 4π and 6π electrocyclization reactions of dienyl diketones for the synthesis of cyclopentenones and 2H-Pyrans. The Journal of Organic Chemistry. 79: 10296-302. PMID 25325706 DOI: 10.1021/Jo501914W |
0.493 |
|
| 2014 |
Carlsen PN, Mann TJ, Hoveyda AH, Frontier AJ. Synthesis of (±)-tetrapetalone A-Me aglycon. Angewandte Chemie (International Ed. in English). 53: 9334-8. PMID 25045072 DOI: 10.1002/Anie.201404410 |
0.834 |
|
| 2014 |
Vaidya T, Cheng R, Carlsen PN, Frontier AJ, Eisenberg R. Cationic cyclizations and rearrangements promoted by a heterogeneous gold catalyst. Organic Letters. 16: 800-3. PMID 24432741 DOI: 10.1021/Ol403542K |
0.798 |
|
| 2014 |
Ciesielski J, Frontier A. The phomactin natural products from isolation to total synthesis: A review Organic Preparations and Procedures International. 46: 214-251. DOI: 10.1080/00304948.2014.903142 |
0.729 |
|
| 2014 |
Leboeuf D, Ciesielski J, Frontier AJ. Gold(I)-catalyzed iodination of arenes Synlett. 25: 399-402. DOI: 10.1055/S-0034-1380682 |
0.776 |
|
| 2014 |
Brooks JL, Huang YW, Frontier AJ. Preparation of 5-hydroxycyclopentenones via conjugate addition-initiated nazarov cyclization Organic Syntheses. 91: 93-105. DOI: 10.1002/0471264229.Os091.09 |
0.514 |
|
| 2013 |
Spencer WT, Vaidya T, Frontier AJ. Beyond the Divinyl Ketone: Innovations in the Generation and Nazarov Cyclization of Pentadienyl Cation Intermediates. European Journal of Organic Chemistry. 2013. PMID 24348092 DOI: 10.1002/Ejoc.201300134 |
0.807 |
|
| 2013 |
Ciesielski J, Lebœuf D, Stern HA, Frontier AJ. Gold (III) Chloride-Catalyzed 6-endo-trig Oxa-Michael Addition Reactions for Diastereoselective Synthesis of Fused Tetrahydropyranones. Advanced Synthesis & Catalysis. 355: 2077-2082. PMID 24032002 DOI: 10.1002/Adsc.201300265 |
0.803 |
|
| 2013 |
Ciesielski J, Gandon V, Frontier AJ. Cascade cyclizations of acyclic and macrocyclic alkynones: studies toward the synthesis of phomactin A. The Journal of Organic Chemistry. 78: 9541-52. PMID 23724905 DOI: 10.1021/Jo4007514 |
0.824 |
|
| 2013 |
Lebœuf D, Theiste E, Gandon V, Daifuku SL, Neidig ML, Frontier AJ. Efficient Nazarov cyclization/Wagner-Meerwein rearrangement terminated by a Cu(II)-promoted oxidation: synthesis of 4-alkylidene cyclopentenones. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 4842-8. PMID 23436470 DOI: 10.1002/Chem.201203396 |
0.493 |
|
| 2013 |
Lebœuf D, Wright CM, Frontier AJ. Reagent control of [1,2]-Wagner-Meerwein shift chemoselectivity following the Nazarov cyclization: application to the total synthesis of enokipodin B. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 4835-41. PMID 23436444 DOI: 10.1002/Chem.201203395 |
0.428 |
|
| 2012 |
Brooks JL, Frontier AJ. Cyclization cascades initiated by 1,6-conjugate addition. Journal of the American Chemical Society. 134: 16551-3. PMID 23004564 DOI: 10.1021/Ja308451Y |
0.524 |
|
| 2012 |
Spencer WT, Frontier AJ. Cycloaromatization protocol for synthesis of polysubstituted phenol derivatives: method development and mechanistic studies. The Journal of Organic Chemistry. 77: 7730-6. PMID 22891882 DOI: 10.1021/Jo3010952 |
0.797 |
|
| 2012 |
Ciesielski J, Cariou K, Frontier AJ. A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A. Organic Letters. 14: 4082-5. PMID 22853449 DOI: 10.1021/Ol3017116 |
0.838 |
|
| 2012 |
Lebœuf D, Gandon V, Ciesielski J, Frontier AJ. Experimental and theoretical studies on the Nazarov cyclization/Wagner-Meerwein rearrangement sequence. Journal of the American Chemical Society. 134: 6296-308. PMID 22471833 DOI: 10.1021/Ja211970P |
0.762 |
|
| 2012 |
Malona JA, Cariou K, Spencer WT, Frontier AJ. Total synthesis of (±)-rocaglamide via oxidation-initiated Nazarov cyclization. The Journal of Organic Chemistry. 77: 1891-908. PMID 22283818 DOI: 10.1021/Jo202366C |
0.824 |
|
| 2012 |
Lautens M, Newman SG, Lebœuf D, Huang J, Gandon V, Frontier AJ. Advances in Nazarov Cyclizations through Control of [1,2]-Migrations Synfacts. 8: 57-57. DOI: 10.1055/S-0031-1289508 |
0.382 |
|
| 2011 |
Lebœuf D, Huang J, Gandon V, Frontier AJ. Using Nazarov electrocyclization to stage chemoselective [1,2]-migrations: stereoselective synthesis of functionalized cyclopentenones. Angewandte Chemie (International Ed. in English). 50: 10981-5. PMID 21953873 DOI: 10.1002/Anie.201104870 |
0.46 |
|
| 2011 |
Trost BM, Frontier AJ, Thiel OR, Yang H, Dong G. Total synthesis of bryostatins: the development of methodology for the atom-economic and stereoselective synthesis of the ring C subunit. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 9762-76. PMID 21793057 DOI: 10.1002/Chem.201002898 |
0.822 |
|
| 2011 |
Brooks JL, Caruana PA, Frontier AJ. Conjugate addition-initiated Nazarov cyclization. Journal of the American Chemical Society. 133: 12454-7. PMID 21780785 DOI: 10.1021/Ja205440X |
0.826 |
|
| 2011 |
Huang J, Lebœuf D, Frontier AJ. Understanding the fate of the oxyallyl cation following Nazarov electrocyclization: sequential Wagner-Meerwein migrations and the synthesis of spirocyclic cyclopentenones. Journal of the American Chemical Society. 133: 6307-17. PMID 21466152 DOI: 10.1021/Ja111504W |
0.547 |
|
| 2011 |
Vaidya T, Manbeck GF, Chen S, Frontier AJ, Eisenberg R. Divergent reaction pathways of a cationic intermediate: rearrangement and cyclization of 2-substituted furyl and benzofuryl enones catalyzed by iridium(III). Journal of the American Chemical Society. 133: 3300-3. PMID 21322633 DOI: 10.1021/Ja111317Q |
0.654 |
|
| 2011 |
Spencer WT, Levin MD, Frontier AJ. Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes. Organic Letters. 13: 414-7. PMID 21155592 DOI: 10.1021/Ol1027255 |
0.817 |
|
| 2011 |
Brooks JL, Caruana PA, Frontier AJ. Nazarov Cyclizations of Dienyl Diketones Initiated by ConjugateAddition Synfacts. 2011: 1091-1091. DOI: 10.1055/S-0030-1261134 |
0.472 |
|
| 2011 |
Trost BM, Frontier AJ, Thiel OR, Yang H, Dong G. ChemInform Abstract: Total Synthesis of Bryostatins: The Development of Methodology for the Atom-Economic and Stereoselective Synthesis of the Ring C Subunit. Cheminform. 43: no-no. DOI: 10.1002/chin.201202195 |
0.773 |
|
| 2011 |
Vaidya T, Eisenberg R, Frontier AJ. Catalytic nazarov cyclization: The state of the art Chemcatchem. 3: 1531-1548. DOI: 10.1002/Cctc.201100137 |
0.489 |
|
| 2010 |
Atesin AC, Zhang J, Vaidya T, Brennessel WW, Frontier AJ, Eisenberg R. Synthesis, characterization, and catalytic properties of new electrophilic iridium(III) complexes containing the (R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl ligand. Inorganic Chemistry. 49: 4331-42. PMID 20361755 DOI: 10.1021/Ic100300Y |
0.566 |
|
| 2010 |
Vaidya T, Atesin AC, Herrick IR, Frontier AJ, Eisenberg R. A highly reactive dicationic iridium(III) catalyst for the polarized Nazarov cyclization reaction. Angewandte Chemie (International Ed. in English). 49: 3363-6. PMID 20358570 DOI: 10.1002/Anie.201000100 |
0.801 |
|
| 2010 |
Zhang J, Vaidya T, Brennessel WW, Frontier AJ, Eisenberg R. Dicationic palladium(II) complexes as active lewis acid catalysts for polarized nazarov cyclization Organometallics. 29: 3341-3349. DOI: 10.1021/Om100274G |
0.491 |
|
| 2010 |
Ciesielski J, Canterbury DP, Frontier AJ. ChemInform Abstract: β-Iodoallenolates as Springboards for Annulation Reactions. Cheminform. 41. DOI: 10.1002/chin.201008030 |
0.719 |
|
| 2009 |
Canterbury DP, Herrick IR, Um J, Houk KN, Frontier AJ. A Torquoselective Extrusion of Isoxazoline N-Oxides. Application to the Synthesis of Aryl Vinyl and Divinyl Ketones for Nazarov Cyclization. Tetrahedron. 65: 3165-3179. PMID 20161228 DOI: 10.1016/J.Tet.2008.10.003 |
0.836 |
|
| 2009 |
Ciesielski J, Canterbury DP, Frontier AJ. Beta-iodoallenolates as springboards for annulation reactions. Organic Letters. 11: 4374-7. PMID 19736911 DOI: 10.1021/Ol901721Y |
0.794 |
|
| 2009 |
Malona JA, Cariou K, Frontier AJ. Nazarov cyclization initiated by peracid oxidation: the total synthesis of (+/-)-rocaglamide. Journal of the American Chemical Society. 131: 7560-1. PMID 19445456 DOI: 10.1021/Ja9029736 |
0.827 |
|
| 2009 |
Bitar AY, Frontier AJ. Formal synthesis of (+/-)-roseophilin. Organic Letters. 11: 49-52. PMID 19053717 DOI: 10.1021/Ol802329Y |
0.845 |
|
| 2009 |
Bitar AY, Frontier AJ. Formal Synthesis of ()-Roseophilin Synfacts. 2009: 824-824. DOI: 10.1055/S-0029-1217579 |
0.822 |
|
| 2009 |
Canterbury DP, Herrick IR, Um J, Houk KN, Frontier AJ. ChemInform Abstract: A Torquoselective Extrusion of Isoxazoline N-Oxides. Application to the Synthesis of Aryl Vinyl and Divinyl Ketones for Nazarov Cyclization. Cheminform. 40. DOI: 10.1002/chin.200933137 |
0.817 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.824 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Bitar AY, Frontier AJ. ChemInform Abstract: Formal Synthesis of (.+-.)-Roseophilin (I). Cheminform. 40. DOI: 10.1002/chin.200919190 |
0.377 |
|
| 2009 |
Canterbury DP, Frontier AJ, Um JM, Cheong PH, Goldfeld DA, Huhn RA, Houk KN. ChemInform Abstract: Origins of Stereoselectivity in the Oxido-Alkylidenation of Alkynes. Cheminform. 40. DOI: 10.1002/chin.200910073 |
0.767 |
|
| 2009 |
Canterbury DP, Frontier AJ, Um JM, Cheong PH, Goldfeld DA, Huhn RA, Houk KN. ChemInform Abstract: Origins of Stereoselectivity in the Oxido-Alkylidenation of Alkynes. Cheminform. 40. DOI: 10.1002/chin.200910073 |
0.767 |
|
| 2009 |
Canterbury DP, Frontier AJ, Um JM, Cheong PH, Goldfeld DA, Huhn RA, Houk KN. ChemInform Abstract: Origins of Stereoselectivity in the Oxido-Alkylidenation of Alkynes. Cheminform. 40. DOI: 10.1002/chin.200910073 |
0.767 |
|
| 2008 |
Canterbury DP, Frontier AJ, Um JM, Cheong PH, Goldfeld DA, Huhn RA, Houk KN. Origins of stereoselectivity in the oxido-alkylidenation of alkynes. Organic Letters. 10: 4597-600. PMID 18798638 DOI: 10.1021/Ol8019154 |
0.749 |
|
| 2008 |
He W, Herrick IR, Atesin TA, Caruana PA, Kellenberger CA, Frontier AJ. Polarizing the Nazarov cyclization: the impact of dienone substitution pattern on reactivity and selectivity. Journal of the American Chemical Society. 130: 1003-11. PMID 18161974 DOI: 10.1021/Ja077162G |
0.796 |
|
| 2008 |
He W, Huang J, Sun X, Frontier AJ. Total synthesis of (+/-)-merrilactone A. Journal of the American Chemical Society. 130: 300-8. PMID 18067294 DOI: 10.1021/Ja0761986 |
0.553 |
|
| 2008 |
He W, Herrick IR, Atesin TA, Caruana PA, Kellenberger CA, Frontier AJ. Lewis Acid Catalyzed Nazarov Cyclization of Dienones Bearing Polar Substituents Synfacts. 2008: 400-400. DOI: 10.1055/S-2008-1042869 |
0.391 |
|
| 2007 |
Jiang C, Frontier AJ. Stereoselective synthesis of pyrrolidine derivatives via reduction of substituted pyrroles. Organic Letters. 9: 4939-42. PMID 17960937 DOI: 10.1021/Ol701962W |
0.485 |
|
| 2007 |
Huang J, Frontier AJ. Development of a Nazarov cyclization/Wagner-Meerwein rearrangement sequence for the stereoselective synthesis of spirocycles. Journal of the American Chemical Society. 129: 8060-1. PMID 17555319 DOI: 10.1021/Ja0716148 |
0.478 |
|
| 2007 |
Trost BM, Yang H, Thiel OR, Frontier AJ, Brindle CS. Synthesis of a ring-expanded bryostatin analogue. Journal of the American Chemical Society. 129: 2206-7. PMID 17279751 DOI: 10.1021/Ja067305J |
0.814 |
|
| 2007 |
He W, Huang J, Sun X, Frontier AJ. Total synthesis of (+/-)-merrilactone A via catalytic Nazarov cyclization. Journal of the American Chemical Society. 129: 498-9. PMID 17227006 DOI: 10.1021/Ja068150I |
0.555 |
|
| 2007 |
Frontier A, He W, Huang J, Sun X. Synthesis of (±)-Merrilactone A Synfacts. 2007: 0669-0669. DOI: 10.1055/S-2007-968603 |
0.304 |
|
| 2007 |
Frontier A, Malona J, Colbourne J. Catalytic Nazarov Cyclization of Heteroaromatic Compounds Synfacts. 2007: 0186-0186. DOI: 10.1055/S-2006-958970 |
0.786 |
|
| 2007 |
Caruana PA, Frontier AJ. Palladium(II)- and mercury(II)-catalyzed rearrangements of propargyl acetates Tetrahedron. 63: 10646-10656. DOI: 10.1016/J.Tet.2007.08.008 |
0.8 |
|
| 2006 |
Malona JA, Colbourne JM, Frontier AJ. A general method for the catalytic nazarov cyclization of heteroaromatic compounds. Organic Letters. 8: 5661-4. PMID 17107097 DOI: 10.1021/Ol062403V |
0.826 |
|
| 2006 |
Janka M, He W, Haedicke IE, Fronczek FR, Frontier AJ, Eisenberg R. Tandem Nazarov cyclization-michael addition sequence catalyzed by an Ir(III) complex. Journal of the American Chemical Society. 128: 5312-3. PMID 16620081 DOI: 10.1021/Ja058772O |
0.634 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/S-2006-941865 |
0.56 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/S-2006-941865 |
0.56 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/s-2006-941865 |
0.361 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/s-2006-941865 |
0.361 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/s-2006-941865 |
0.361 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/s-2006-941865 |
0.361 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/s-2006-941865 |
0.361 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/s-2006-941865 |
0.361 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/S-2006-941865 |
0.56 |
|
| 2006 |
Frontier A, Eisenberg R, Janka M, He W, Haedicke I, Fronczek F. Ir(III)-Catalyzed Tandem Nazarov Cyclization/Michael Addition Synfacts. 2006: 0683-0683. DOI: 10.1055/s-2006-941865 |
0.361 |
|
| 2005 |
Frontier AJ, Collison C. The Nazarov cyclization in organic synthesis. Recent advances Tetrahedron. 61: 7577-7606. DOI: 10.1016/J.Tet.2005.05.019 |
0.388 |
|
| 2005 |
Janka M, He W, Frontier AJ, Flaschenriem C, Eisenberg R. Preorganization in the Nazarov cyclization: The role of adjacent coordination sites in the highly Lewis acidic catalyst [IrMe(CO)(dppe)(DIB)] (BAr4 f)2 Tetrahedron. 61: 6193-6206. DOI: 10.1016/J.Tet.2005.03.114 |
0.572 |
|
| 2004 |
Janka M, He W, Frontier AJ, Eisenberg R. Efficient catalysis of Nazarov cyclization using a cationic iridium complex possessing adjacent labile coordination sites. Journal of the American Chemical Society. 126: 6864-5. PMID 15174845 DOI: 10.1021/Ja049643V |
0.536 |
|
| 2004 |
He W, Sun X, Frontier AJ. Polarizing the Nazarov Cyclization: Efficient Catalysis under Mild Conditions [J. Am. Chem.Soc.2003,125, 14278−14279]. Journal of the American Chemical Society. 126: 10493-10493. DOI: 10.1021/Ja0457258 |
0.419 |
|
| 2004 |
Caruana PA, Frontier AJ. Dearomatization of furans via [2,3]-Still-Wittig rearrangement Tetrahedron. 60: 10921-10926. DOI: 10.1016/J.Tet.2004.09.029 |
0.813 |
|
| 2003 |
He W, Sun X, Frontier AJ. Polarizing the Nazarov cyclization: efficient catalysis under mild conditions. Journal of the American Chemical Society. 125: 14278-9. PMID 14624567 DOI: 10.1021/Ja037910B |
0.515 |
|
| 2001 |
Inoue M, Carson MW, Frontier AJ, Danishefsky SJ. Total synthesis and determination of the absolute configuration of frondosin B. Journal of the American Chemical Society. 123: 1878-89. PMID 11456808 DOI: 10.1021/Ja0021060 |
0.623 |
|
| 2001 |
Trost BM, Frontier AJ. ChemInform Abstract: Atom Economical Syntheses of Oxygen Heterocycles via Tandem Palladium-Catalyzed Reactions. Cheminform. 32: no-no. DOI: 10.1002/chin.200111129 |
0.439 |
|
| 2001 |
Trost BM, Frontier AJ. ChemInform Abstract: Atom Economical Syntheses of Oxygen Heterocycles via Tandem Palladium-Catalyzed Reactions. Cheminform. 32: no-no. DOI: 10.1002/chin.200111129 |
0.439 |
|
| 2000 |
Inoue M, Frontier AJ, Danishefsky SJ. The Total Synthesis of Frondosin B. Angewandte Chemie (International Ed. in English). 39: 761-764. PMID 10760861 DOI: 10.1002/(Sici)1521-3757(20000218)112:4<777::Aid-Ange777>3.0.Co;2-K |
0.503 |
|
| 2000 |
Frontier AJ, Raghavan S, Danishefsky SJ. A highly stereoselective total synthesis of hispidospermidin: Derivation of a pharmacophore model Journal of the American Chemical Society. 122: 6151-6159. DOI: 10.1021/Ja9944960 |
0.575 |
|
| 2000 |
Trost BM, Frontier AJ. Atom economical syntheses of oxygen heterocycles via tandem palladium-catalyzed reactions [2] Journal of the American Chemical Society. 122: 11727-11728. DOI: 10.1021/Ja0022268 |
0.41 |
|
| 1998 |
Frontier AJ, Danishefsky SJ, Koppel GA, Meng D. A useful α, α' - Annulation reaction of enamines Tetrahedron. 54: 12721-12736. DOI: 10.1016/S0040-4020(98)00788-1 |
0.448 |
|
| 1997 |
Frontier AJ, Raghavan S, Danishefsky SJ. Stereocontrolled total synthesis of hispidospermidin Journal of the American Chemical Society. 119: 6686-6687. DOI: 10.1021/Ja970889S |
0.59 |
|
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