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.
β¦ LIBER β¦
Mechanistic Studies on Thiaminase I: 1. The Stereochemical Course of the Reaction
β 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
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Mechanistic Studies on Thiaminase I: Ide
β
Min Wu; Elizabeth T. Papish; Tadhg P. Begley
π
Article
π
2000
π
Elsevier Science
π
English
β 46 KB
Control of the steric course of the Witt
β
L.D. Bergelson; M.M. Shemyakin
π
Article
π
1963
π
Elsevier Science
π
French
β 648 KB
On the stereochemical aspects of the 1,1
β
Albert Padwa; Auguste Rodriguez
π
Article
π
1981
π
Elsevier Science
π
French
β 175 KB
A Study of the Stereochemical Course of
β
Masahiro Murakami; Hideyuki Igawa
π
Article
π
2002
π
John Wiley and Sons
π
German
β 79 KB
## Abstract The stereochemical course of __Ξ²__βoxygen elimination of an organorhodium(I) complex was investigated through the Rhβcatalyzed addition of phenylboronic acid to a chiral propargyl acetate to produce an allene. The degree of chirality transfer suggests that the __Ξ²__βoxygen elimination t
Mechanistic studies on the rhodium compl
β
A.M. Trzeciak; J.J. ZiΓ³Εkowski
π
Article
π
1983
π
Elsevier Science
β 943 KB
Stereochemical Course of the Allylic Hyd
β
Gyoosoon Park; Jang Cheol Hwang; Woo Sik Jung; Choon Sup Ra
π
Article
π
2006
π
John Wiley and Sons
β 14 KB