Role of the Heteroatoms in the Complex Metal Hydride Reduction of 2-t-Butyl-1,3-dioxan-5-one and 3-Oxoquinolizidine: Comparison of Their Reactivity and Stereochemistry with Those of the Corresponding Carbocyclic Compounds-Reference-Cited by-同舟云学术

Role of the Heteroatoms in the Complex Metal Hydride Reduction of 2-t-Butyl-1,3-dioxan-5-one and 3-Oxoquinolizidine: Comparison of Their Reactivity and Stereochemistry with Those of the Corresponding Carbocyclic Compounds

Published:1999-02 Issue:2 Volume:72 Page:285-288
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Senda Yasuhisa,Sakurai Hiroshi,Itoh Hiroki

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/72/2/72_2_285/_pdf

Reference21 articles.

1. Diastereofacial selection in nucleophilic additions to unsymmetrically substituted trigonal carbons

2. An electronic interpretation of the stereochemistry of the reduction of cyclohexanones

3. Electronic effects on the stereochemistry of attack on trigonal atoms in six membered rings

4. Stereochemistry of nucleophilic addition to cyclohexanone. The importance of two-electron stabilizing interactions

5. Origin of π-facial stereoselectivity of hydride reduction of cyclohexanones. A new interpretation based on quantitative analysis of exterior frontier orbital extension

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