Kinetics, stereochemistry, and mechanism of the sodium borohydride reduction of alkyl-substituted cyclohexanones-Reference-Cited by-同舟云学术

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Kinetics, stereochemistry, and mechanism of the sodium borohydride reduction of alkyl-substituted cyclohexanones

Published:1970-11 Issue:23 Volume:92 Page:6894-6904
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Rickborn Bruce,Wuesthoff Michael T.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00726a028

Cited by 114 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Peroxygenase-Catalyzed Allylic Oxidation Unlocks Telescoped Synthesis of (1S,3R)-3-Hydroxycyclohexanecarbonitrile;ACS Catalysis;2024-02-13

2. Unravelling the underlying mechanism of the reduction of aldehydes/ketones with metal borohydride in an aprotic solvent;Chemical Communications;2024

3. Static to inducibly dynamic stereocontrol: The convergent use of racemic β-substituted ketones;Science;2020-08-28

4. Stereoselective Reductions of 3-Substituted Cyclobutanones: A Comparison between Experiment and Theory;The Journal of Organic Chemistry;2020-05-22

5. Hidden Boron Catalysis: Nucleophile-Promoted Decomposition of HBpin;Organic Letters;2020-05-07

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