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Reduction by a model of NAD(P)H: XI. Stereochemistry of a lactate dehydrogenase-model reaction

✍ Scribed by A. Ohno; T. Kimura; S.G. Kim; H. Yamamoto; S. Oka; Y. Ohnishi


Book ID
107873681
Publisher
Elsevier Science
Year
1977
Tongue
English
Weight
484 KB
Volume
6
Category
Article
ISSN
0045-2068

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## 2,3-Dihydro-2,2,4-trimethylthieno[3,2-b]pyridinium I-oxide iodide (1) has been reacted with various inorganic and organic hydride donors. It has been found that the stereochemistry of reaction is controlled by the orientation of the sulfinyl dipole, and the relative bulkiness of substituents pl