The preference for anti over gauche migration in the Baeyer-Villiger reaction

Journal of Organic Chemistry

Volumn 69, Issue 21, 2004, Pages 7148-7156

  Snowden, Michelle ^a   Bermudez, Amy ^a   Kelly, David R ^b   Radkiewicz Poutsma, Jennifer L ^a  

^a OLD DOMINION UNIVERSITY   (United States)

^b CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ENERGY GAP; OPTIMIZATION; STEREOCHEMISTRY;

ENERGY BARRIERS; GAUCHE MIGRATION; STEREOSELECTIVITY; TRANSITION STRUCTURES;

CHEMICAL REACTIONS;

ACETALDEHYDE; ANION; CARBONYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CATION; COBALT; COPPER; FLAVOPROTEIN; FORMALDEHYDE; FORMIC ACID; HYDROGEN PEROXIDE; HYDROXYL GROUP; KETONE DERIVATIVE; LACTONE DERIVATIVE; PALLADIUM; PEROXIDE; SELENIUM;

AB INITIO CALCULATION; ARTICLE; BAEYER VILLIGER REACTION; CATALYST; CONFORMATION; ENANTIOSELECTIVITY; ENERGY; REACTION ANALYSIS; STEREOCHEMISTRY;

CYCLIZATION; KETONES; MODELS, MOLECULAR; MOLECULAR CONFORMATION; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 5444255112     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0491307     Document Type: Article

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