Highly Chemoselective Reductive Amination of Carbonyl Compounds Promoted by InCl3/Et3SiH/MeOH System
Author:
Affiliation:
1. Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, People's republic of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo8016082
Reference52 articles.
1. Reduction of activated conjugated alkenes by the InCl3–NaBH4 reagent system
2. Remarkably Selective Reduction of the α,β-Carbon−Carbon Double Bond in Highly Activated α,β,γ,δ-Unsaturated Alkenes by the InCl3−NaBH4 Reagent System
3. Use of indium hydride (Cl2InH) for chemoselective reduction of the carboncarbon double bond in conjugated alkenes
4. Indium(III) Chloride−Sodium Borohydride System: A Convenient Radical Reagent for an Alternative to Tributyltin Hydride System
5. Selective reductive cleavage of 2,3-epoxybromides by the InCl3–NaBH4 reagent system
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