Preparation of medium- and large-ring lactones. SmI2-induced cyclization of ω-(α-bromoacyloxy) aldehydes-Reference-Cited by-同舟云学术

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Preparation of medium- and large-ring lactones. SmI2-induced cyclization of ω-(α-bromoacyloxy) aldehydes

Published:1986-01 Issue:33 Volume:27 Page:3889-3890
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tabuchi Takanori,Kawamura Kisa,Inanaga Junji,Yamaguchi Masaru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Synthesis of macrolides

2. Tetrahedron report number 190

3. Ring-closure reactions. I. Kinetics of lactone formation in the range of seven- to twelve-membered rings

4. A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-ring Lactonization

5. A translactonization route to macrocyclic lactones

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1. Recent Applications of Kagan's Reagent (SmI2) in Natural Product Synthesis;Efficiency in Natural Product Total Synthesis;2018-08-06

2. Formation of Alcohols and Phenols by Alkylation of Carbonyl Compounds;Comprehensive Organic Transformations;2018-02-28

3. Enantioselective Medium-Ring Lactone Synthesis through an NHC-Catalyzed Intramolecular Desymmetrization of Prochiral 1,3-Diols;ACS Catalysis;2017-10-09

4. Samarium( II ) iodide;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-21

5. Samarium( II ) iodide;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-20

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