A highly diastereoselective tandem Michael-Michael addition reaction in a rotameric ring system: steric acceleration due to conformation locking
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Solutions 51 – 100;Strategies and Solutions to Advanced Organic Reaction Mechanisms;2019
2. Acid-mediated coupling of γ-hydroxybutenolides and aldehydes: synthesis of a new class of spirocyclic ketal-lactones;Tetrahedron Letters;2012-12
3. ChemInform Abstract: A Highly Diastereoselective Tandem Michael-Michael Addition Reaction in a Rotameric Ring System: Steric Acceleration Due to Conformation Locking.;ChemInform;2010-08-19
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