Stereoselective Synthesis of Polysubstituted Tetrahydrofurans by Radical Cyclization of Epoxides Using a Transition-Metal Radical Source. Application to the Total Synthesis of (±)-Methylenolactocin and (±)-Protolichesterinic Acid-Reference-Cited by-同舟云学术

Stereoselective Synthesis of Polysubstituted Tetrahydrofurans by Radical Cyclization of Epoxides Using a Transition-Metal Radical Source. Application to the Total Synthesis of (±)-Methylenolactocin and (±)-Protolichesterinic Acid

Published:1998-04-15 Issue:9 Volume:63 Page:2829-2834
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mandal Pijus Kumar¹,Maiti Gourhari¹,Roy Subhas Chandra¹

Affiliation:

1. Department of Organic Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Calcutta-700 032, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971526d

Reference21 articles.

1. Intramolecular free radical cyclisations onto vinyl ethers. A method for the synthesis of β-oxy-γ-butyrolactones

2. Homolytic carbocyclization by use of a heterogeneous supported organotin catalyst. A new synthetic route to 2-alkoxytetrahydrofurans and .gamma.-butyrolactones

3. Recent advances in the preparation and synthetic applications of oxiranes

4. Selective Generation of Free Radicals from Epoxides Using a Transition-Metal Radical. A Powerful New Tool for Organic Synthesis

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