Zirconocene-mediated deoxygenative ring contractions of vinyl-substituted carbohydrates: An expedient route to enantiomerically pure, densely functionalized 4-to-8-membered carbocycles
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference39 articles.
1. Zirconium-mediated, highly diastereoselective ring contraction of carbohydrate derivatives: synthesis of highly functionalized, enantiomerically pure carbocycles
2. Reaction of zirconocene dichloride with alkyllithiums or alkyl grignard reagents as a convenient method for generating a “zirconocene” equivalant and its use in zirconium-promoted cyclization of alkenes, alkynes, dienes, enynes, and diynes
3. Formation of Carbon-Carbon Bonds using Zirconocene-Butene Complex (”Cp2Zr”) as a Synthetic Tool
4. Practical zirconium-mediated deprotective method of allyl groups
5. Preparation and regio- and diastereoselective reactions of allylic zirconium reagents from allylic ether derivatives
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