Cp2TiCl-Mediated Selective Reduction of α,β-Epoxy Ketones-Reference-Cited by-同舟云学术

Cp2TiCl-Mediated Selective Reduction of α,β-Epoxy Ketones

Published:2001-01-11 Issue:3 Volume:66 Page:1046-1048
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hardouin Christophe¹,Chevallier Floris¹,Rousseau Bernard¹,Doris Eric¹

Affiliation:

1. CEA/Saclay, Service des Molécules Marquées, Bât. 547, Département de Biologie Cellulaire et Moléculaire, 91191 Gif sur Yvette Cedex, France eric.doris@cea.fr

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001358g

Reference20 articles.

1. An asymmetric synthesis of enantiomerically pure (S)-(+)-linalool (3,7-dimethyl-1,6-octadien-3-ol) and a formal synthesis of (R)-(-)-linalool

2. Stereochemistry of the reductive alkylation of .alpha.,.beta.-epoxy ketones

Cited by 67 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. Electrooxidative α-hydroxymethylation of ketones with dimethylformamide as the carbon source;Green Chemistry;2023

2. Ring‐Opening Reactions of Epoxides With Titanium(III) Reagents;Organic Reactions;2022-12-29

3. The reaction of β,γ−epoxy alcohols with titanium(III) reagents. A proposed role for intramolecular hydrogen bonding;Tetrahedron;2019-11

4. Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin;Angewandte Chemie International Edition;2018-05-30

5. Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin;Angewandte Chemie;2018-05-30