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- W2209374013 abstract "Publisher Summary This chapter discusses the interpretation of enzyme reaction stereochemistry. Examples have been selected from the literature to illustrate broad principles that may be applicable to large classes of enzymes. Particular emphasis is given to enzyme systems for which X-ray crystallographic measurements provide a structural context in which to evaluate possible mechanistic interpretations of stereochemical trends. The chapter uses the Cahn–Ingold–Prelog convention for assigning absolute configuration to chiral centers. Chemically identical substituents at prochiral centers are designated according to Hanson's convention. Since 1970, there has been a dramatic increase in the number of enzymes of known stereochemistry, owing to the broad application of numerous elegant methods of stereochemical analysis. An important challenge facing bioorganic chemists is to distinguish between those cases in which the stereochemical features of an enzymic reaction are functionally neutral and the cases that reflect underlying mechanistic advantages unavailable through alternative stereochemical modes." @default.
- W2209374013 created "2016-06-24" @default.
- W2209374013 creator A5006517302 @default.
- W2209374013 creator A5018293878 @default.
- W2209374013 date "1990-01-01" @default.
- W2209374013 modified "2023-10-10" @default.
- W2209374013 title "7 Stereochemistry of Enzyme -Catalyzed Reactions at Carbon" @default.
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