A Mechanistic Study on the Catalytic, Asymmetric α-Bromination of Acid Chlorides

Autor:	Cajetan Dogo-Isonagie, Tefsit Bekele, Stefan France, Jamison Wolfer, Anthony Weatherwax, Andrew E. Taggi, Daniel H. Paull, Travis Dudding, Thomas Lectka
Rok vydání:	2007
Předmět:	Molecular model Chemistry Organic Chemistry Enantioselective synthesis Halogenation Transition state Catalysis Kinetic resolution chemistry.chemical_compound Computational chemistry Organic chemistry Physical and Theoretical Chemistry Enantiomeric excess Derivatization
Zdroj:	European Journal of Organic Chemistry. 2007:1091-1100
ISSN:	1099-0690 1434-193X
DOI:	10.1002/ejoc.200600819
Popis:	The mechanism of the catalytic, asymmetric α-bromination of acid chlorides is probed through a series of crossover experiments, ion-pairing tests, and kinetic resolution studies to shed light on the factors that contribute to, and limit the production of, optically-active α-bromo esters. In order to understand better the observed sense of induction, as well as the high degree of enantiomeric excess exhibited by these products, extensive molecular modeling is employed on the relevant transition states. Finally, the usefulness of the α-bromo ester products is demonstrated by their simple derivatization into chiral epoxides.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
Databáze:	OpenAIRE
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