Asymmetric synthesis using α-sulfinylcarbanions. I. Synthesis of optically active alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Chemistry of sulfoxides and related compounds. XXXIV. Mechanism of sulfonium ylide reactions. Synthesis of cyclopropanes and oxiranes of high optical purity
2. The sterochemistry of the reaction of α-lithio-sulphoxides (α-sulphinyl carbanions) with ketones
3. Asymmetric Reductions. VII. the Action of the Grignard Reagent from (+)-1-chloro-2-methylbutane on a Series of Alkyl Phenyl Ketones1-3
4. Optical Rotatory Dispersion Studies. LXIX.1 The Absolute Configuration of the 2-Methylcyclohexanols and Some Observations on a Twist Form in the Conformational Equilibrium of 2-Methylcyclohexanone
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1. Access towards enantiopure α,α-difluoromethyl alcohols by means of sulfoxides as traceless chiral auxiliaries;Chemical Communications;2018
2. On the nature of the chain-extending species in organolithium initiated stereospecific reagent-controlled homologation reactions using α-chloroalkyl aryl sulfoxides;Tetrahedron Letters;2015-06
3. 3.20 Stoichiometric Auxiliary Ligands for Metals and Main Group Elements: Ligands for Lithium;Comprehensive Chirality;2012
4. Enantioselective Organocatalytic Rearrangement of α-Acyloxy- β-keto Sulfides to α-Acyloxy Thioesters;Advanced Synthesis & Catalysis;2010-11-16
5. p-Tolylsulfinylmethyllithium;Encyclopedia of Reagents for Organic Synthesis;2008-09-15
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