The most reactive amide as a transition-state mimic for cis - Trans interconversion

Journal of the American Chemical Society

Volumn 137, Issue 2, 2015, Pages 926-930

  Komarov, Igor V ^a   Yanik, Stanislav ^a   Ishchenko, Aleksandr Yu ^a,b   Davies, John E ^c   Goodman, Jonathan M ^c   Kirby, Anthony J ^c  

^a TARAS SHEVCHENKO NATIONAL UNIVERSITY OF KYIV   (Ukraine)

^b ENAMINE LTD   (Ukraine)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ENZYME ACTIVITY; FUNCTIONAL GROUPS;

AMIDE GROUPS; INTERCONVERSIONS; METHYL GROUP; PARENT COMPOUNDS; RARE CLASS; SUBSTITUTION PATTERNS; TRANSITION STATE; TWISTED AMIDES;

AMIDES;

1 AZATRICYCLO[3.3.1.1 ]DECAN 2 ONE; AMIDE; METHYL GROUP; UNCLASSIFIED DRUG; 1-AZATRICYCLO(3.3.1.1(3,7))DECAN-2-ONE; FUSED HETEROCYCLIC RINGS; HETEROCYCLIC COMPOUND;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CIS TRANS INTERCONVERSION; CONFORMATION; CRYSTAL STRUCTURE; PROTEIN FOLDING; PROTEIN FUNCTION; PYROLYSIS; SUBSTITUTION REACTION; SYNTHESIS; CHEMISTRY; STEREOISOMERISM;

AMIDES; AZA COMPOUNDS; HETEROCYCLIC COMPOUNDS, 3-RING; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 84921512347     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja511460a     Document Type: Article

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