Regio- and diastereoselective addition of allylic thioethers to aldehydes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Diastereoselective Synthesis of Protected syn 1,3-Diols: Preparation of the C16−C24 Portion of Dolabelides
2. Synthesis of protected syn 1,3-diols by intramolecular conjugate addition to vinyl sulfones
3. Condensation of β-hydroxy sulfones and vinyl sulfones with aldehydes and ketones using phenyllithium as base
4. Tandem Conjugate Addition−Elimination for the Diastereoselective Synthesis of 4E-Alkenyl syn-1,3-Diols
5. Regional convergence in the reaction of heterosubstituted allylic carbanions via allylic aluminum and boron ate complexes
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1. Pummerer-Type Reactions as Powerful Tools in Organic Synthesis;Molecular Rearrangements in Organic Synthesis;2015-10-02
2. Reactions of Aldehydes and Ketones and their Derivatives;Organic Reaction Mechanisms Series;2011-12-06
3. Synthesis of Modified Methyl Furanosides by Intramolecular Oxa-Michael Reaction followed by Pummerer Rearrangement;The Journal of Organic Chemistry;2010-04-12
4. A two-step synthesis of allylic syn 1,3-diols via an intramolecular oxa-Michael reaction followed by a modified Julia olefination;Tetrahedron Letters;2010-01
5. ChemInform Abstract: Regio- and Diastereoselective Addition of Allylic Thioethers to Aldehydes.;ChemInform;2009-06-02
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