Acid-catalyzed aldol-Meerwein–Ponndorf–Verley-etherification reactions—access to defined configured quaternary stereogenic centers
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference99 articles.
1. Highly diastereoselective acetal cleavages using novel reagents prepared from organoaluminum and pentafluorophenol
2. Highly Diastereoselective Catalytic Meerwein−Ponndorf−Verley Reductions
3. A Two-Directional Approach to a (−)-Dictyostatin C11−C23 Segment: Development of a Highly Diastereoselective, Kinetically-Controlled Meerwein−Ponndorf−Verley Reduction
4. Asymmetric 1,7-Hydride Shift: The Highly Asymmetric Reduction of α,β-Unsaturated Ketones to Secondary Alcohols via a Novel Tandem Michael Addition−Meerwein−Ponndorf−Verley Reduction
5. Highly enantioselective synthesis of 1,3-mercapto alcohols from α,β-unsaturated ketones: asymmetric bifunctional group exchange reaction
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