Hydrazine sulphate: a cheap and efficient catalyst for the regioselective ring-opening of epoxides. A metal-free procedure for the preparation of β-alkoxy alcohols-Reference-Cited by-同舟云学术

Hydrazine sulphate: a cheap and efficient catalyst for the regioselective ring-opening of epoxides. A metal-free procedure for the preparation of β-alkoxy alcohols

Published:2008-03 Issue:10 Volume:49 Page:1694-1697
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Leitão Alcino J.L.,Salvador Jorge A.R.,Pinto Rui M.A.,Sá e Melo M. Luísa

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference36 articles.

1. Synthetically Useful Reactions of Epoxides

2. The Logic of Chemical Synthesis;Corey,1989

3. Enantiospecific synthesis of an aziridinobenzazocinone, an advanced intermediate containing the core nucleus of FR900482 and FK973

4. An Effective Strategy for the Synthesis of 6-O-(2-Amino-2-deoxy-.alpha.-D-glucopyranosyl)-D-chiro- and -D-myo-inositol 1-Phosphate Related to Putative Insulin Mimetics

5. Efficient procedures for the large-scale preparation of (1S,2S)-trans-2-methoxycyclohexanol, a key chiral intermediate in the synthesis of tricyclic β-lactam antibiotics

Cited by 24 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. Visible photons for the regioselective nucleophilic ring opening of epoxides;Green Chemistry;2024

2. Exposed Zinc Sites on Hybrid ZnIn₂S₄@CdS Nanocages for Efficient Regioselective Photocatalytic Epoxide Alcoholysis;Angewandte Chemie International Edition;2023-04-19

3. Exposed Zinc Sites on Hybrid ZnIn₂S₄@CdS Nanocages for Efficient Regioselective Photocatalytic Epoxide Alcoholysis;Angewandte Chemie;2023-04-19

4. Synthesis of Carvone Derivatives and In Silico and In Vitro Screening of Anti-Inflammatory Activity in Murine Macrophages;International Journal of Molecular Sciences;2023-01-23

5. Enzymatic synthesis and chemical inversion provide both enantiomers of bioactive epoxydocosapentaenoic acids;Journal of Lipid Research;2018-11