An effective protocol for the synthesis enantiomerically pure 4-substituted oxetane-2-ones-Reference-Cited by-同舟云学术

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An effective protocol for the synthesis enantiomerically pure 4-substituted oxetane-2-ones

Published:2013-06 Issue:24 Volume:69 Page:4990-4993
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bałakier Tomasz,Chaładaj Wojciech,Jurczak Janusz,Adamus Grażyna,Kowalczuk Marek

Funder

European Regional Development Fund

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Novel polymerization of β-butyrolactone initiated by potassium naphthalenide in the presence of a crown ether or a cryptand

2. Anionic Ring-Opening Polymerization of β-Alkoxymethyl-Substituted β-Lactones

3. Drent, E.; Kragtwijk, E. Shell Internationale Research, European Patent Application EP 577206; Chem. Abstr. 1994, 120, 191517c.

4. Synthesis of β-Lactones: A Highly Active and Selective Catalyst for Epoxide Carbonylation

5. [Lewis Acid]+[Co(CO)4] Complexes: A Versatile Class of Catalysts for Carbonylative Ring Expansion of Epoxides and Aziridines

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4. Diversifying Polyhydroxyalkanoates – End-Group and Side-Chain Functionality;Current Organic Synthesis;2017-09-28

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