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Mechanistic Studies on Thiaminase I: 1. The Stereochemical Course of the Reaction

✍ Scribed by R. Nicewonger; A. Rammelsberg; C.A. Costello; T.P. Begley


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
262 KB
Volume
23
Category
Article
ISSN
0045-2068

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πŸ“œ SIMILAR VOLUMES


Mechanistic Studies on Thiaminase I: Ide
✍ Min Wu; Elizabeth T. Papish; Tadhg P. Begley πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 English βš– 46 KB

Thiaminase I catalyzes the decomposition of thiamin under basic conditions in the absence of the nucleophilic cosubstrate. The product of this reaction was identified as the adduct resulting from the displacement of the thiazole moiety of thiamin by the ring opened form of thiamin.

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## Abstract The stereochemical course of __Ξ²__‐oxygen elimination of an organorhodium(I) complex was investigated through the Rh‐catalyzed addition of phenylboronic acid to a chiral propargyl acetate to produce an allene. The degree of chirality transfer suggests that the __Ξ²__‐oxygen elimination t