The stereochemistry and absolute configuration of abienol

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Synthesis, stereochemistry and absolute configuration of deodarols and deodarones

The stereochemistry and absolute configuration of the four deodarols and two deodarones derived from R-(+)-limonene is described. © 2002 Elsevier Science Ltd. All rights reserved.

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The absolute configuration of methylmalonyl coenzyme A and stereochemistry of the methymalonyl coenzyme A mutase reaction.

Rropionyl coenzyme A was carboxylated with epimerasefree carboxylase, and the resulting methylmalonyl coenzyme A (a) was reduced with Raney nickel. Isolation of (-)(R)-P-hydroxyisobutyric acid N-phenylcarbamate (11) from the reaction mixture showed that methylmalonyl coenzyme A (a) has the (S) configuration. Propionyl coenzyme A was also converted to deuteriosuccinate with a DrO extract of a be...

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The Absolute Configuration of Methylmalonyl Coenzyme A and Stereochemistry of the Methylmalonyl Coenzyme A Mutase Reaction*

Rropionyl coenzyme A was carboxylated with epimerasefree carboxylase, and the resulting methylmalonyl coenzyme A (a) was reduced with Raney nickel. Isolation of (-)(R)-P-hydroxyisobutyric acid N-phenylcarbamate (11) from the reaction mixture showed that methylmalonyl coenzyme A (a) has the (S) configuration. Propionyl coenzyme A was also converted to deuteriosuccinate with a DrO extract of a be...

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ژورنال

عنوان ژورنال: Australian Journal of Chemistry

سال: 1966

ISSN: 0004-9425

DOI: 10.1071/ch9661535