13.1. Reduction of a Ketone Using Sodium Borohydride. Control of a Reaction by TLC-Reference-Cited by-同舟云学术

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13.1. Reduction of a Ketone Using Sodium Borohydride. Control of a Reaction by TLC

Published:2016-12-16 Issue: Volume: Page:776-780
ISSN:
Container-title:Comprehensive Organic Chemistry Experiments for the Laboratory Classroom
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Author:

Constantino Luis¹²,Dias Catarina¹,Valente Emília¹

Affiliation:

1. Faculty of Pharmacy, Universidade de Lisboa Av. Professor Gama Pinto 1649-003 Lisbon Portugal

2. Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa Av. Professor Gama Pinto 1649-003 Lisbon Portugal constant@ff.ulisboa.pt

Publisher

The Royal Society of Chemistry

Link

https://books.rsc.org/books/edited-volume/chapter-pdf/1688308/bk9781849739634-00776.pdf

Reference5 articles.

1. The Kinetics of 20-Keto Reduction in 11α-Acetoxypregnane-3,20-dione by Sodium Borohydride

2. Limited alkoxy group exchange in tetraalkoxyborohydrides: Evidence against the four-centre transition state in the borohydride reduction of ketones

3. Stereochemistry and mechanism of ketone reductions by hydride reagents

4. Reduction of ketones by sodium borohydride in the absence of protic solvents. Inter versus intramolecular mechanism

5. Recent progress in biocatalysis for asymmetric oxidation and reduction

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