Barbara Zajc to Stereoisomerism
This is a "connection" page, showing publications Barbara Zajc has written about Stereoisomerism.
Connection Strength
1.100
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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: 0.154
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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: 0.123
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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: 0.116
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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: 0.111
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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: 0.104
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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: 0.086
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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: 0.079
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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: 0.074
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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: 0.069
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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: 0.067
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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: 0.054
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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: 0.018
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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: 0.014
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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: 0.013
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Custer L, Zajc B, Sayer JM, Cullinane C, Phillips DR, Cheh AM, Jerina DM, Bohr VA, Mazur SJ. Stereospecific differences in repair by human cell extracts of synthesized oligonucleotides containing trans-opened 7,8,9, 10-tetrahydrobenzo[a]pyrene 7,8-diol 9,10-epoxide N2-dG adduct stereoisomers located within the human K-ras codon 12 sequence. Biochemistry. 1999 Jan 12; 38(2):569-81.
Score: 0.010
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Page JE, Zajc B, Oh-hara T, Lakshman MK, Sayer JM, Jerina DM, Dipple A. Sequence context profoundly influences the mutagenic potency of trans-opened benzo[a]pyrene 7,8-diol 9,10-epoxide-purine nucleoside adducts in site-specific mutation studies. Biochemistry. 1998 Jun 23; 37(25):9127-37.
Score: 0.010