Stereoselective synthesis of 2,3-epoxy alcohols mediated by a remote sulfinyl group-Reference-Cited by-同舟云学术

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Stereoselective synthesis of 2,3-epoxy alcohols mediated by a remote sulfinyl group

Published:2010-02 Issue:8 Volume:66 Page:1581-1585
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

García Ruano José Luis,Martín-Castro Ana M.,Tato Francisco,Torrente Esther,Tocco M. Giovanna,Florio Saverio,Capriati Vito

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Epoxy ketones as versatile building blocks in organic synthesis

2. Highly Enantio- and Diastereoselective One-Pot Synthesis of Acyclic Epoxy Alcohols with Three Contiguous Stereocenters

3. One-Pot Asymmetric Synthesis of Acyclic Chiral Epoxy Alcohols via Tandem Vinylation−Epoxidation with Dioxygen

4. Oxiranyl Anions and Aziridinyl Anions

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1. Lithiated oxazolinyloxiranes and oxazolinylaziridines: key players in organic synthesis;Pure and Applied Chemistry;2014-06-18

2. α-Lithiated α-Heterosubstituted 2-Alkyloxazolines: Key Players in Organic Synthesis;Synlett;2013-05-10

3. Vinylogous Aldol Reaction of a Silyloxydiene Promoted by Sulfoxides, as Lewis Bases: 1,4–asymmetric Induction Mediated by a Remote Methylsulfinyl Group;Current Organic Chemistry;2013-04-01

4. The Sulfinyl Group as a Remote Chiral Auxiliary in Stereoselective Conjugate Additions of Alkyl Groups to α-Methylidene Carbonyl Compounds Initiated by Et3B/O2;European Journal of Organic Chemistry;2013-02-07

5. Reactions of Aldehydes and Ketones and their Derivatives;Organic Reaction Mechanisms Series;2012-12-04

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