Stereospecific Redox Reaction Directed by a Sulfinyl Group-Reference-Cited by-同舟云学术

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Stereospecific Redox Reaction Directed by a Sulfinyl Group

Published:1997-01-01 Issue:1 Volume:120 Page:445-446
ISSN:1042-6507
Container-title:Phosphorus, Sulfur, and Silicon and the Related Elements
language:en
Short-container-title:Phosphorus, Sulfur, and Silicon and the Related Elements

Author:

Yamazaki Norimasa¹²³⁴⁵,Okamura Mutsuo¹²³⁴⁵,Kawai Yasushi¹²³⁴⁵,Mikata Yuji¹²³⁴⁵,Ohno Atsuyoshi¹²³⁴⁵

Affiliation:

1. a Institute for Chemical Research , Kyoto University , Uji, Kyoto 611, Japan

2. b Department of Chemistry, Faculty of Science , Niigata University , Niigata 950-21, Japan

3. c Institute for Chemical Research , Kyoto University , Uji, Kyoto 611, Japan

4. d Department of Chemistry, Faculty of Science , Nara Women's University , Nara 630, Japan

5. e Institute for Chemical Research , Kyoto University , Uji, Kyoto 611, Japan

Publisher

Informa UK Limited

Subject

Inorganic Chemistry,Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10426509708545590

Reference3 articles.

1. NAD(P+/NAD(P)H Models. 83. Molecular Asymmetry with a Carbonyl Group: Electronically Controlled Stereochemistry in the Reaction of NAD(P)+/NAD(P)H Analogs

2. NAD(P)+-NAD(P)H models. 61. An interconversion between central and axial chiralities as evidence for a functional model of chemical evolution of an enzyme

3. NAD(P)+-NAD(P)H models. 84. Stereochemistry controlled by the electronic effect from a sulfinyl group

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