Barbara Zajc to Stereoisomerism
This is a "connection" page, showing publications Barbara Zajc has written about Stereoisomerism.
Connection Strength
0.958
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Wei W, Khangarot RK, Stahl L, Veresmortean C, Pradhan P, Yang L, Zajc B. Generating Stereodiversity: Diastereoselective Fluorination and Highly Diastereoselective Epimerization of a-Amino Acid Building Blocks. Org Lett. 2018 06 15; 20(12):3574-3578.
Score: 0.137
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Kumar R, Singh G, Todaro LJ, Yang L, Zajc B. E- or Z-Selective synthesis of 4-fluorovinyl-1,2,3-triazoles with fluorinated second-generation Julia-Kocienski reagents. Org Biomol Chem. 2015 Feb 07; 13(5):1536-49.
Score: 0.109
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Chowdhury M, Mandal SK, Banerjee S, Zajc B. Synthesis of regiospecifically fluorinated conjugated dienamides. Molecules. 2014 Apr 10; 19(4):4418-32.
Score: 0.103
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Singh G, Kumar R, Swett J, Zajc B. Modular synthesis of N-vinyl benzotriazoles. Org Lett. 2013 Aug 16; 15(16):4086-9.
Score: 0.098
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Kumar R, Zajc B. Stereoselective synthesis of conjugated fluoro enynes. J Org Chem. 2012 Oct 05; 77(19):8417-27.
Score: 0.092
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Ghosh AK, Zajc B. Fluorinated 1-phenyl-1H-tetrazol-5-yl sulfone derivatives as general reagents for fluoroalkylidene synthesis. J Org Chem. 2009 Nov 20; 74(22):8531-40.
Score: 0.076
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del Solar M, Ghosh AK, Zajc B. Fluoro-Julia olefination as a mild, high-yielding route to alpha-fluoro acrylonitriles. J Org Chem. 2008 Nov 07; 73(21):8206-11.
Score: 0.070
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Ghosh AK, Lagisetty P, Zajc B. Direct synthesis of 8-fluoro purine nucleosides via metalation-fluorination. J Org Chem. 2007 Oct 26; 72(22):8222-6.
Score: 0.065
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Zajc B, Kake S. Exceptionally mild, high-yield synthesis of alpha-fluoro acrylates. Org Lett. 2006 Sep 28; 8(20):4457-60.
Score: 0.061
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Ghosh AK, Zajc B. High-yield synthesis of fluorinated benzothiazolyl sulfones: general synthons for fluoro-julia olefinations. Org Lett. 2006 Apr 13; 8(8):1553-6.
Score: 0.059
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Zajc B, Grahek R, Kocijan A, Lakshman MK, Kosmrlj J, Lah J. Evaluation of the enantiomeric resolution of 7,8-dihydroxy-7,8-dihydrobenzo[a]-pyrene and its 6-fluoro and 6-bromo derivatives on polysaccharide-derived stationary phases. J Org Chem. 2003 Apr 18; 68(8):3291-4.
Score: 0.048
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Lakshman MK, Keeler JC, Ngassa FN, Hilmer JH, Pradhan P, Zajc B, Thomasson KA. Highly diastereoselective synthesis of nucleoside adducts from the carcinogenic benzo[a]pyrene diol epoxide and a computational analysis. J Am Chem Soc. 2007 Jan 10; 129(1):68-76.
Score: 0.016
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Okazaki T, Laali KK, Zajc B, Lakshman MK, Kumar S, Baird WM, Dashwood WM. Stable ion study of benzo[a]pyrene (BaP) derivatives: 7,8-dihydro-BaP, 9,10-dihydro-BaP and its 6-halo derivatives, 1- and 3-methoxy-9,10-dihydro-BaP-7(8H)-one, as well as the proximate carcinogen BaP 7,8-dihydrodiol and its dibenzoate, combined with a comparative DNA binding study of regioisomeric (1-, 4-, 2-) pyrenylcarbinols. Org Biomol Chem. 2003 May 07; 1(9):1509-16.
Score: 0.012
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Kramata P, Zajc B, Sayer JM, Jerina DM, Wei CS. A single site-specific trans-opened 7,8,9,10-tetrahydrobenzo[a]pyrene 7,8-diol 9,10-epoxide N2-deoxyguanosine adduct induces mutations at multiple sites in DNA. J Biol Chem. 2003 Apr 25; 278(17):14940-8.
Score: 0.012