Synthesis of enantiomerically pure 1,3-diols by stereoselective reduction of β-ketosulfoxides. Influence of a stereogenic hydroxylic centre at the δ-position-Reference-Cited by-同舟云学术

Synthesis of enantiomerically pure 1,3-diols by stereoselective reduction of β-ketosulfoxides. Influence of a stereogenic hydroxylic centre at the δ-position

Published:1997-10 Issue:19 Volume:8 Page:3283-3292
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

García Ruano JoséL.,González-Vadillo Ana M.,Maestro M.Carmen

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference20 articles.

1. Reduction of β-hydroxysulfoxides: Application to the synthesis of optically active epoxides

2. Reduction of chiral .beta.-hydroxy sulfoxides: application to the synthesis of both enantiomers of 4-substituted butenolides

3. 1,3-asymmetric induction in the reduction ofα-alkyl β-Ketosulfoxides with DIBAL/ZnBr2

4. Some Applications of Chiralβ-Ketosulfoxides in Asymmetric Synthesis

5. Stereoselective reductions of 2-keto sulfoxides with hydrides

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. ChemInform Abstract: Synthesis of Enantiomerically Pure 1,3-Diols by Stereoselective Reduction of β-Ketosulfoxides. Influence of a Stereogenic Hydroxylic Center at the δ-Position.;ChemInform;2010-06-24

2. An improved method for the asymmetric protonation of enolates with chiral α-sulfinyl alcohols/trifluoroethanol;Tetrahedron: Asymmetry;2001-06

3. Highly stereoselective additions of sulfur stabilized carbanions to [(S)R]-2-(p-tolylsulfinyl)cyclohexanones;Tetrahedron: Asymmetry;2000-11

4. Synthesis of enantiomerically pure 2-amino alcohols from amino acids mediated by sulfoxides;Tetrahedron: Asymmetry;2000-08

5. Asymmetric Synthesis of Biologically Interesting Compounds Utilizing Chiral Sulfoxides;Sulfur reports;1999-09