Chemoselective reductive deoxygenation of α,β-unsaturated ketones and allyl alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Reductive displacement of allylic acetates by hydride transfer via catalytic activation by palladium(0) complexes
2. Ionic Hydrogenation with Triethylsilane-Trifluoroacetic Acid-Ammonium Fluoride or Triethylsilane-Pyridinium Poly(hydrogen fluoride)1
3. Selective Reduction of Diaryl or Aryl Alkyl Alcohols in the Presence of Primary Hydroxyl or Ester Groups by Etherated Boron Trifluoride-Triethylsilane System
4. Highly diastereocontrolled reduction of ketones by means of hydrosilanes. Practical synthesis of optically active 1,2-diols and 2-amino alcohols of threo or erythro configuration
5. Reduction of aldehydes and ketones to alcohols and hydrocarbons through use of the organosilane-boron trifluoride system
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