Year |
Citation |
Score |
2021 |
Shao H, Chakrabarty S, Qi X, Takacs JM, Liu P. Ligand Conformational Flexibility Enables Enantioselective Tertiary C-B Bond Formation in the Phosphonate-Directed Catalytic Asymmetric Alkene Hydroboration. Journal of the American Chemical Society. PMID 33750118 DOI: 10.1021/jacs.1c01303 |
0.678 |
|
2019 |
Chakrabarty S, Palencia H, Morton MD, Carr RO, Takacs JM. Facile access to functionalized chiral secondary benzylic boronic esters catalytic asymmetric hydroboration. Chemical Science. 10: 4854-4861. PMID 31183035 DOI: 10.1039/C8Sc05613G |
0.847 |
|
2019 |
Bochat AJ, Shoba VM, Takacs JM. Ligand-Controlled Regiodivergent Enantioselective Rhodium-Catalyzed Alkene Hydroboration. Angewandte Chemie (International Ed. in English). PMID 31067341 DOI: 10.1002/Anie.201903308 |
0.831 |
|
2018 |
Chakrabarty S, Takacs JM. Phosphonate-Directed Catalytic Asymmetric Hydroboration: Delivery of Boron to the More Substituted Carbon, Leading to Chiral Tertiary Benzylic Boronic Esters. Acs Catalysis. 8: 10530-10536. PMID 31134137 DOI: 10.1021/Acscatal.8B03591 |
0.776 |
|
2018 |
Hoang GL, Zhang S, Takacs JM. Rhodium-catalyzed asymmetric hydroboration of γ,δ-unsaturated amide derivatives: δ-borylated amides. Chemical Communications (Cambridge, England). PMID 29696267 DOI: 10.1039/C8Cc01563E |
0.838 |
|
2017 |
Hoang GL, Takacs JM. Enantioselective γ-borylation of unsaturated amides and stereoretentive Suzuki-Miyaura cross-coupling. Chemical Science. 8: 4511-4516. PMID 28758006 DOI: 10.1039/C7Sc01093A |
0.825 |
|
2017 |
Chakrabarty S, Takacs JM. Synthesis of Chiral Tertiary Boronic Esters: Phosphonate-Directed Catalytic Asymmetric Hydroboration of Trisubstituted Alkenes. Journal of the American Chemical Society. PMID 28414243 DOI: 10.1021/Jacs.7B02324 |
0.731 |
|
2017 |
Shoba VM, Takacs JM. Remarkably Facile Borane-Promoted, Rhodium-Catalyzed Asymmetric Hydrogenation of Tri- and Tetrasubstituted Alkenes. Journal of the American Chemical Society. PMID 28394591 DOI: 10.1021/Jacs.7B02581 |
0.813 |
|
2016 |
Marichev KO, Takacs JM. Ruthenium-Catalyzed Amination of Secondary Alcohols using Borrowing Hydrogen Methodology. Acs Catalysis. 6: 2205-2210. PMID 28936364 DOI: 10.1021/Acscatal.6B00175 |
0.389 |
|
2015 |
Shoba VM, Thacker NC, Bochat AJ, Takacs JM. Synthesis of Chiral Tertiary Boronic Esters by Oxime-Directed Catalytic Asymmetric Hydroboration. Angewandte Chemie (International Ed. in English). PMID 26662460 DOI: 10.1002/Anie.201509137 |
0.823 |
|
2015 |
Thacker NC, Shoba VM, Geis AE, Takacs JM. Surprisingly Facile C-H Activation in the Course of Oxime-Directed Catalytic Asymmetric Hydroboration. Tetrahedron Letters. 56: 3306-3310. PMID 26120214 DOI: 10.1016/J.Tetlet.2014.12.076 |
0.787 |
|
2015 |
Hoang GL, Yang ZD, Smith SM, Pal R, Miska JL, Pérez DE, Pelter LS, Zeng XC, Takacs JM. Enantioselective desymmetrization via carbonyl-directed catalytic asymmetric hydroboration and Suzuki-Miyaura cross-coupling. Organic Letters. 17: 940-3. PMID 25642639 DOI: 10.1021/Ol503764D |
0.837 |
|
2014 |
Yang ZD, Pal R, Hoang GL, Zeng XC, Takacs JM. Mechanistic Insights into Carbonyl-Directed Rhodium-Catalyzed Hydroboration: ab Initio Study of a Cyclic γ,δ-Unsaturated Amide. Acs Catalysis. 4: 763-773. PMID 24804151 DOI: 10.1021/Cs401023J |
0.799 |
|
2012 |
Thacker NC, Moteki SA, Takacs JM. Ligand scaffold optimization of a supramolecular hydrogenation catalyst: Analyzing the influence of key structural subunits on reactivity and selectivity. Acs Catalysis. 2: 2743-2752. PMID 23525350 DOI: 10.1021/Cs300465U |
0.798 |
|
2012 |
Smith SM, Hoang GL, Pal R, Bani Khaled MO, Pelter LS, Zeng XC, Takacs JM. γ-Selective directed catalytic asymmetric hydroboration of 1,1-disubstituted alkenes. Chemical Communications (Cambridge, England). 48: 12180-2. PMID 23145431 DOI: 10.1039/C2Cc36199J |
0.835 |
|
2012 |
Moteki SA, Toyama K, Liu Z, Ma J, Holmes AE, Takacs JM. Two-stage optimization of a supramolecular catalyst for catalytic asymmetric hydroboration. Chemical Communications (Cambridge, England). 48: 263-5. PMID 22089694 DOI: 10.1039/C1Cc16146F |
0.721 |
|
2012 |
Thacker NC, Molnár-Tóth J, Miska JL, Barletta RG, Takacs JM. Preparation of D-cycloserine and 13C-labeled D-cycloserine Heterocycles. 86: 1575-1582. DOI: 10.3987/Com-12-12553 |
0.737 |
|
2011 |
Smith SM, Uteuliyev M, Takacs JM. Catalytic asymmetric hydroboration of β,γ-unsaturated Weinreb amides: striking influence of the borane. Chemical Communications (Cambridge, England). 47: 7812-4. PMID 21637887 DOI: 10.1039/C1Cc11746G |
0.621 |
|
2010 |
Smith SM, Takacs JM. Remarkable levels of enantioswitching in catalytic asymmetric hydroboration. Organic Letters. 12: 4612-5. PMID 20863120 DOI: 10.1021/Ol101932Q |
0.649 |
|
2010 |
Smith SM, Takacs JM. Amide-directed catalytic asymmetric hydroboration of trisubstituted alkenes. Journal of the American Chemical Society. 132: 1740-1. PMID 20092272 DOI: 10.1021/Ja908257X |
0.694 |
|
2010 |
Smith SM, Takacs JM. Asymmetric Hydroboration of Trisubstituted Alkenes Synfacts. 2010: 546-546. DOI: 10.1055/S-0029-1219697 |
0.68 |
|
2008 |
Smith SM, Thacker NC, Takacs JM. Efficient amide-directed catalytic asymmetric hydroboration. Journal of the American Chemical Society. 130: 3734-5. PMID 18311977 DOI: 10.1021/Ja710492Q |
0.827 |
|
2008 |
Zhang Q, Takacs JM. Click-connected ligand scaffolds: macrocyclic chelates for asymmetric hydrogenation. Organic Letters. 10: 545-8. PMID 18189407 DOI: 10.1021/Ol702890S |
0.413 |
|
2008 |
Moteki SA, Takacs JM. Exploiting self-assembly for ligand-scaffold optimization: substrate-tailored ligands for efficient catalytic asymmetric hydroboration. Angewandte Chemie (International Ed. in English). 47: 894-7. PMID 18098260 DOI: 10.1002/Anie.200703127 |
0.693 |
|
2008 |
Smith SM, Thacker NC, Takacs JM. Rhodium-Catalyzed Asymmetric Hydroboration Synfacts. 2008: 623-623. DOI: 10.1055/S-2008-1078388 |
0.846 |
|
2008 |
Takacs JM, Moteki SA, Reddy DS. Chirality-Directed Self-Assembly: An Enabling Strategy for Ligand Scaffold Optimization Supramolecular Catalysis. 235-253. DOI: 10.1002/9783527621781.ch9 |
0.654 |
|
2006 |
Moteki SA, Wu D, Chandra KL, Reddy DS, Takacs JM. TADDOL-derived phosphites and phosphoramidites for efficient rhodium-catalyzed asymmetric hydroboration. Organic Letters. 8: 3097-100. PMID 16805561 DOI: 10.1021/Ol061117G |
0.762 |
|
2006 |
Atkins JM, Moteki SA, Dimagno SG, Takacs JM. Single enantiomer, chiral donor-acceptor metal complexes from bisoxazoline pseudoracemates. Organic Letters. 8: 2759-62. PMID 16774250 DOI: 10.1021/Ol060836S |
0.764 |
|
2006 |
Takacs JM, Chaiseeda K, Moteki SA, Reddy DS, Wu D, Chandra K. Rhodium-catalyzed asymmetric hydrogenation using self-assembled chiral bidentate ligands Pure and Applied Chemistry. 78: 501-509. DOI: 10.1351/Pac200678020501 |
0.726 |
|
2006 |
Takacs J, Moteki S, Wu D, Chandra K, Reddy D. Efficient Rhodium-Catalyzed Asymmetric Hydroboration Synfacts. 2006: 0923-0923. DOI: 10.1055/S-2006-949270 |
0.749 |
|
2005 |
Takacs JM, Hrvatin PM, Atkins JM, Reddy DS, Clark JL. The selective formation of neutral, heteroleptic zinc(II) complexes via self-discrimination of chiral bisoxazoline racemates and pseudoracemates New Journal of Chemistry. 29: 263-265. DOI: 10.1039/B413439G |
0.615 |
|
2005 |
Takacs JM, Venkataraman S, Andrews RN, Pelter LSW. N-heterocyclic carbene-palladium catalysts for the bisdiene cyclization-trapping reaction with sulfonamides under thermal and microwave conditions Journal of Organometallic Chemistry. 690: 6205-6209. DOI: 10.1016/J.Jorganchem.2005.08.048 |
0.453 |
|
2005 |
Takacs JM, Layek S, Palencia H, Andrews RN. Improved turnover numbers in palladium-catalyzed bisdiene cyclization-trapping using N-heterocyclic carbene ligands Advanced Synthesis and Catalysis. 347: 1937-1942. DOI: 10.1002/Adsc.200505136 |
0.816 |
|
2004 |
Takacs JM, Han J. Improving catalyst scope: use of multiple aniline substrates to optimize a palladium-catalyzed bisdiene cyclization. Organic Letters. 6: 3099-102. PMID 15330597 DOI: 10.1021/Ol0488791 |
0.498 |
|
2004 |
Takacs JM, Reddy DS, Moteki SA, Wu D, Palencia H. Asymmetric catalysis using self-assembled chiral bidentate P,P-ligands. Journal of the American Chemical Society. 126: 4494-5. PMID 15070348 DOI: 10.1021/Ja049873+ |
0.789 |
|
2004 |
Palencia H, Garcia-Jimenez F, Takacs JM. Suzuki-Miyaura coupling with high turnover number using an N-acyl-N-heterocyclic carbene palladacycle precursor Tetrahedron Letters. 45: 3849-3853. DOI: 10.1016/J.Tetlet.2004.03.138 |
0.778 |
|
2003 |
Dumitru R, Palencia H, Schroeder SD, DeMontigny BA, Takacs JM, Rasche ME, Miner JL, Ragsdale SW. Targeting methanopterin biosynthesis to inhibit methanogenesis. Applied and Environmental Microbiology. 69: 7236-41. PMID 14660371 DOI: 10.1128/Aem.69.12.7236-7241.2003 |
0.741 |
|
2003 |
Takacs JM, Leonov AP. Palladium-catalyzed bisdiene carbocyclizations: a facile [3 + 2] cycloaddition reaction mode. Organic Letters. 5: 4317-20. PMID 14601989 DOI: 10.1021/Ol035569U |
0.697 |
|
2003 |
Takacs JM, Schroeder SD, Han J, Gifford M, Jiang XT, Saleh T, Vayalakkada S, Yap AH. Controlling mode selectivity in palladium-catalyzed bisdiene carbocyclizations: optimizing for cyclization-trapping over cycloisomerization. Organic Letters. 5: 3595-8. PMID 14507181 DOI: 10.1021/Ol035253M |
0.43 |
|
2003 |
Takacs JM, Jiang XT. The Wacker reaction and related alkene oxidation reactions Current Organic Chemistry. 7: 369-396. DOI: 10.2174/1385272033372851 |
0.392 |
|
2003 |
Takacs JM, Jiang XT, Leonov AP. Palladium-catalyzed regiocontrolled and stereoselective alkylations of bis(trifluoroethyl) malonates with dienyl alcohols Tetrahedron Letters. 44: 7075-7079. DOI: 10.1016/S1268-7731(03)00074-2 |
0.67 |
|
2002 |
Takacs JM, Xu Z, Jiang XT, Leonov AP, Theriot GC. Carbon nucleophiles in the Mitsunobu reaction. Mono- and dialkylation of bis(2,2,2-trifluoroethyl) malonates. Organic Letters. 4: 3843-5. PMID 12599473 DOI: 10.1021/Ol0266626 |
0.69 |
|
2002 |
Takacs JM, Vayalakkada S, Mehrman SJ, Kingsbury CL. Iron-catalyzed enediene carbocyclizations. The total synthesis of (-)-gibboside Tetrahedron Letters. 43: 8417-8420. DOI: 10.1016/S0040-4039(02)01662-3 |
0.375 |
|
1999 |
Bai J, Ducharme S, Leonov A, Liu L, Takacs JM. New organic photorefractive material composed of a charge-transporting dendrimer and a stilbene chromophore Proceedings of Spie - the International Society For Optical Engineering. 3799: 22-30. |
0.507 |
|
1998 |
Takacs JM, Jaber MR, Clement F, Walters C. A Useful Procedure for the Preparation of (E,E)-2,4-Dienoates: Lithium Hydroxide-Promoted Dienylation by 4-Phosphonocrotonate Journal of Organic Chemistry. 63: 6757-6760. DOI: 10.1021/Jo980841C |
0.532 |
|
1998 |
Takacs JM, Jaber MR, Swanson BJ, Mehrman SJ. Regio- and diastereoselective boron-mediated aldol reactions of chiral α,β,γ,δ-unsaturated N-acyloxazolidinones Tetrahedron Asymmetry. 9: 4313-4324. DOI: 10.1016/S0957-4166(98)00459-5 |
0.482 |
|
1998 |
Takacs JM, Jaber MR, Strakhov AV, Athalye RV. Palladium-catalyzed bisdiene carbocyclizations: Cycloisomerizations of bisdienes bearing an ester substituent Tetrahedron Letters. 39: 5003-5006. DOI: 10.1016/S0040-4039(98)00979-4 |
0.484 |
|
1998 |
Bai J, Ducharme S, Goonesekera A, Leonov AP, Lu L, Takacs JM. Synthesis and characterization of dendrimers for potential photorefractive applications American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. 39: 991. |
0.584 |
|
1998 |
Takacs JM, Boito SC, Myoung YC. Recent applications of catalytic metal-mediated carbocyclizations in asymmetric synthesis Current Organic Chemistry. 2: 233-254. |
0.74 |
|
1997 |
Takacs JM, Clement F, Zhu J, Chandramouli SV, Gong X. Catalytic palladium-mediated bisdiene carbocyclizations: Bisdiene to enediene cycloisomerizations Journal of the American Chemical Society. 119: 5804-5817. DOI: 10.1021/Ja962748G |
0.792 |
|
1997 |
Takacs JM, Lawson EC, Clement F. On the Nature of the Catalytic Palladium-Mediated Elimination of Allylic Carbonates and Acetates To Form 1,3-Dienes Journal of the American Chemical Society. 119: 5956-5957. DOI: 10.1021/Ja962313T |
0.636 |
|
1997 |
Takacs JM, Quincy DA, Shay W, Jones BE, Ross CR. Enantioselective Diels-Alder reactions: Novel constrained bis(oxazoline) ligand-metal triflate catalysts Tetrahedron Asymmetry. 8: 3079-3087. DOI: 10.1016/S0957-4166(97)00323-6 |
0.489 |
|
1997 |
Takacs JM, Lawson EC, Reno MJ, Youngman MA, Quincy DA. Enantioselective Diels-Alder reactions: Room temperature bis(oxazoline)-zinc, -magnesium, and -copper triflate catalysts Tetrahedron Asymmetry. 8: 3073-3078. DOI: 10.1016/S0957-4166(97)00322-4 |
0.465 |
|
1996 |
Takacs JM, Mehrman SJ. Catalytic cobalt-mediated reductive carbocyclizations Tetrahedron Letters. 37: 2749-2752. DOI: 10.1016/0040-4039(96)00421-2 |
0.54 |
|
1995 |
Takacs JM, Weidner JJ, Newsome PW, Takacs BE, Chidambaram R, Shoemaker R. Catalytic Iron-Mediated Enediene Carbocyclizations: Investigations into the Stereoselective Formation of Bicyclic Ring Systems Journal of Organic Chemistry. 60: 3473-3486. DOI: 10.1021/Jo00116A039 |
0.387 |
|
1995 |
Takacs JM, Boito SC. Catalytic iron-mediated enediene carbocyclizations: The enantioselective synthesis of a homologue of the alkaloid (-)-protoemetinol Tetrahedron Letters. 36: 2941-2944. DOI: 10.1016/0040-4039(95)00443-G |
0.477 |
|
1995 |
Takacs JM, Weidner JJ, Newsome PW, Takacs BE, Chidambaram R, Shoemaker R. Catalytic iron-mediated enediene carbocyclizations: Investigations into the stereoselective formation of bicyclic ring systems Journal of Organic Chemistry. 60: 3473-3486. |
0.78 |
|
1994 |
Takacs JM, Lawson EC. Catalytic rhodium-mediated tetraene carbocyclizations Organometallics. 13: 4787-4793. DOI: 10.1021/Om00024A025 |
0.457 |
|
1994 |
Takacs JM, Myoung YC, Anderson LG. Catalytic iron-mediated triene carbocyclizations: Stereoselective five-membered ring forming carbocyclizations Journal of Organic Chemistry. 59: 6928-6942. DOI: 10.1021/Jo00102A016 |
0.772 |
|
1994 |
Takacs JM, Weidner JJ. Reaction of pentadienyltrimethylsilane with N-acyliminium ion intermediates. A convenient route to pentadienyl-substituted lactams Journal of Organic Chemistry. 59: 6480-6483. DOI: 10.1021/Jo00100A064 |
0.368 |
|
1994 |
Takacs JM, Chandramouli SV. Catalytic palladium-mediated tetraene carbocyclizations: The efficient stereochemical control of newly formed methyl-bearing stereocenters Tetrahedron Letters. 35: 9165-9168. DOI: 10.1016/0040-4039(94)88455-2 |
0.706 |
|
1994 |
Takacs JM, Chandramouli SV, Shoemaker R. Catalytic palladium-mediated tetraene carbocyclizations: diastereoselective deuteration and its convenient analysis by a difference spin polarization transfer (DSPT) NMR experiment Tetrahedron Letters. 35: 9161-9164. DOI: 10.1016/0040-4039(94)88454-4 |
0.621 |
|
1993 |
Eckhardt CJ, Peachey NM, Swanson DR, Takacs JM, Khan MA, Gong X, Kim JH, Wang J, Uphaus RA. Separation of chiral phases in monolayer crystals of racemic amphiphiles Nature. 362: 614-616. DOI: 10.1038/362614A0 |
0.305 |
|
1993 |
Takacs JM, Chandramouli SV. Catalytic palladium-mediated tetraene carbocyclizations: 1,2- and 1,4-stereochemical control in a polycyclization reaction Journal of Organic Chemistry. 58: 7315-7317. DOI: 10.1021/Jo00078A001 |
0.7 |
|
1993 |
Takacs JM, Weidner JJ, Takacs BE. Catalytic iron-mediated ene carbocyclizations of trienes: Investigations into the stereoselective formation of some bicyclic lactams and amines. Tetrahedron Letters. 34: 6219-6222. DOI: 10.1016/S0040-4039(00)73714-2 |
0.464 |
|
1992 |
Takacs JM, Zhu J, Chandramouli S. Catalytic palladium-mediated tetraene carbocyclizatioos: The cycloisomerizations of acyclic tetraenes to cyclized trienes Journal of the American Chemical Society. 114: 773-774. DOI: 10.1021/Ja00028A061 |
0.713 |
|
1992 |
Takacs JM, Myoung YC. Catalytic iron-mediated ene carbocyclizations of trienes: enantioselective syntheses of the iridoid monoterpenes (-)-mitsugashiwalactone and (+)-isoiridomyrmecin Tetrahedron Letters. 33: 317-320. DOI: 10.1016/S0040-4039(00)74120-7 |
0.775 |
|
1990 |
Takacs JM, Chandramouli S. Catalytic transition-metal-mediated tetraene carbocyclizations. A new carbocyclization via hydrosilylation? Organometallics. 9: 2877-2880. DOI: 10.1021/Om00161A013 |
0.692 |
|
1990 |
Evans DA, Dow RL, Shih TL, Takacs JM, Zahler R. Total synthesis of the polyether antibiotic ionomycin Journal of the American Chemical Society. 112: 5290-5313. DOI: 10.1021/Ja00169A042 |
0.438 |
|
1990 |
Takacs JM, Helle MA, Sanyal BJ, Eberspacher TA. The magnitude of the stereodirecting effect of an allylic alkoxy-substituent in an amidomercuration cyclization Tetrahedron Letters. 31: 6765-6768. DOI: 10.1016/S0040-4039(00)97166-1 |
0.665 |
|
1990 |
Takacs JM, Zhu J. Catalytic palladium-mediat{approaches the limit}d tetraene carbocyclizations: Enamine trapping reagents Tetrahedron Letters. 31: 1117-1120. DOI: 10.1016/S0040-4039(00)88740-7 |
0.529 |
|
1990 |
Takacs JM, Newsome PW, Kuehn C, Takusagawa F. Catalytic iron-mediated ene carbocyclizations: formal [4+4]-ene reactions of triene esters Tetrahedron. 46: 5507-5522. DOI: 10.1016/S0040-4020(01)87749-8 |
0.818 |
|
1990 |
Takacs BE, Takacs JM. Catalytic iron-mediated ene carbocyclizations of trienes: The stereoselecitve preparation of N-acylpiperidines Tetrahedron Letters. 31: 2865-2868. DOI: 10.1016/0040-4039(90)80168-L |
0.421 |
|
1989 |
Takacs JM, Zhu J. Catalytic palladium-mediated tetraene carbocyclizations The Journal of Organic Chemistry. 54: 5193-5195. DOI: 10.1021/Jo00283A002 |
0.528 |
|
1989 |
Takacs JM, Helle MA, Yang L. A removable auxiliary for amidomercuration reactions: The stereocontrolled preparation of vicinal aminoalcohols Tetrahedron Letters. 30: 1777-1780. DOI: 10.1016/S0040-4039(00)99577-7 |
0.624 |
|
1989 |
Takacs JM, Helle MA, Takusagawa F. A removable auxiliary for amidomercuration reactions: The stereoselective preparation of substituted n-acyl pyrrolidines and piperidines Tetrahedron Letters. 30: 7321-7324. DOI: 10.1016/S0040-4039(00)70687-3 |
0.674 |
|
1987 |
Takacs JM, Anderson LG, Newsome PW. Asymmetric induction in the formal iron-catalyzed [4 + 4] ene reaction: The highly diastereoselective cross-coupling of 1,3-dienes to chiral cyclic acetals Journal of the American Chemical Society. 109: 2542-2544. DOI: 10.1021/Ja00242A065 |
0.808 |
|
1987 |
Takacs JM, Anderson LG. Intramolecular formal iron-catalyzed ene reactions: New and highly stereoselective iron-catalyzed carbocyclizations of triene ethers Journal of the American Chemical Society. 109: 2200-2202. DOI: 10.1021/Ja00241A059 |
0.385 |
|
1987 |
Takacs JM, Anderson LG, Creswell MW, Takacs BE. Intramolecular formal iron-catalyzed ene reactions: The stereoselective and regiocontrolled formation of substituted tetrahydropyrans Tetrahedron Letters. 28: 5627-5630. DOI: 10.1016/S0040-4039(00)96797-2 |
0.52 |
|
1987 |
Takacs JM, Anderson LG, Madhavan GVB, Seely FL. Unusual Ligand Directed Regioselectivity in the Iron Catalyzed Cross Coupling of Allylic Ethers to 2-Substituted 1,3-Dienes† Angewandte Chemie. 26: 1013-1015. DOI: 10.1002/Anie.198710131 |
0.432 |
|
1986 |
Takacs JM, Anderson LG, Madhavan GVB, Creswell MW, Seely FL, Devroy WF. Transition-metal-catalyzed carbon-carbon bond forming reactions: Regio- and chemoselective iron(0)-catalyzed diene to olefin cross-coupling reactions Organometallics. 5: 2395-2398. DOI: 10.1021/Om00142A044 |
0.435 |
|
1986 |
Takacs JM, Helle MA, Seely FL. An improved procedure for the two carbon homologation of esters to α, β-unsaturated esters Tetrahedron Letters. 27: 1257-1260. DOI: 10.1016/S0040-4039(00)84232-X |
0.593 |
|
1981 |
Evans DA, Takacs JM, McGee LR, Ennis MD, Mathre DJ, Bartroli J. Chiral enolate design Pure and Applied Chemistry. 53: 1109-1127. DOI: 10.1351/Pac198153061109 |
0.451 |
|
1980 |
Evans DA, Takacs JM. Enantioselective alkylation of chiral enolates Tetrahedron Letters. 21: 4233-4236. DOI: 10.1016/S0040-4039(00)92870-3 |
0.56 |
|
1979 |
Evans DA, Takacs JM, Hurst KM. Phosphonamide stabilized allylic carbanions. New homoenolate anion equivalents Journal of the American Chemical Society. 101: 371-378. DOI: 10.1021/Ja00496A016 |
0.56 |
|
1978 |
Hudrlik PF, Takacs JM. Reactions of ketones with sodium hydride or potassium hydride in the presence of trimethylsilyl chloride. Preparation of trimethylsilyl enol ethers Journal of Organic Chemistry. 43: 3861-3865. DOI: 10.1002/Chin.197910269 |
0.451 |
|
1978 |
Evans DA, Hurst KM, Takacs JM. New silicon-phosphorus reagents in organic synthesis. Carbonyl and conjugate addition reactions of silicon phosphite esters and related systems Journal of the American Chemical Society. 100: 3467-3477. DOI: 10.1002/Chin.197836247 |
0.505 |
|
1977 |
Evans DA, Hurst KM, Truesdale LK, Takacs JM. The carbonyl insertion reactions of mixed tervalent phosphorus-organosilicon reagents Tetrahedron Letters. 18: 2495-2498. DOI: 10.1016/S0040-4039(01)83802-8 |
0.515 |
|
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