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Angewandte Chemie - International Edition

Volumn 51, Issue 7, 2012, Pages 1724-1727

Stereochemistry of benzylic carbon substitution coupled with ring modification of 2-nitrobenzyl groups as key determinants for fast-cleaving reversible terminators

(9) Stupi, Brian P a Li, Hong a Wang, Jinchun a Wu, Weidong a Morris, Sidney E a,b Litosh, Vladislav A a,d Muniz, Jesse b Hersh, Megan N a Metzker, Michael L a,b,c

a LaserGen Inc (United States)

b Human Genome Sequencing Center (United States)

c BAYLOR COLLEGE OF MEDICINE (United States)

d UNIVERSITY OF ILLINOIS AT CHICAGO (United States)

Author keywords

cleavage reactions; nucleotides; photochemistry; reversible terminators

Indexed keywords

2-NITROBENZYL; BENZYLIC CARBON; CLEAVAGE REACTION; KEY DETERMINANTS; PHOTOCHEMICAL CLEAVAGE; RATE INCREASE; REVERSIBLE TERMINATORS; STEREOSPECIFIC; TERT-BUTYL GROUP;

METHANOL; PHOTOCHEMICAL REACTIONS; STEREOCHEMISTRY;

NUCLEOTIDES;

BENZYL DERIVATIVE; NITROBENZENE DERIVATIVE; NUCLEOTIDE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM;

BENZYL COMPOUNDS; MOLECULAR STRUCTURE; NITROBENZENES; NUCLEOTIDES; STEREOISOMERISM;

EID: 84863020041 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201106516 Document Type: Article

Times cited : (34)

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