A Free Radical Method for Reduction of Cyclohexanones—Preferential Formation of Equatorial Alcohols
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1081/SCC-120020210
Reference12 articles.
1. Formal Synthesis of d-myo-Inositol 1,4,5-Tris(dihydrogen phosphate): Cyclization by an Unusual Ene Reaction and Use of the Bu2SnCl2/Bu2SnH2 Reagent for Generating an Equatorial Alcohol
2. Cyclopentane synthesis and annulation: Intramolecular radical cyclization of acetals
3. Cyclopentane synthesis and annulation II: Radical cyclizations of oxathiolanones
4. Free-radical based cycloalkanol synthesis and annulation from thioacetal precursors
5. Diastereofacial selectivity in reactions of substituted cyclohexyl radicals. An experimental and theoretical study
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