Computational Study on the Reaction Mechanism of the Key Thermal [4 + 4] Cycloaddition Reaction in the Biosynthesis of Epoxytwinol A-Reference-Cited by-同舟云学术

Computational Study on the Reaction Mechanism of the Key Thermal [4 + 4] Cycloaddition Reaction in the Biosynthesis of Epoxytwinol A

Published:2006-02-18 Issue:6 Volume:8 Page:1041-1044
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shiina Isamu¹,Uchimaru Tadafumi¹,Shoji Mitsuru¹,Kakeya Hideaki¹,Osada Hiroyuki¹,Hayashi Yujiro¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Science, and Department of Industrial Chemistry, Faculty of Engineering, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan, Research Institute for Computational Sciences, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8568, Japan, and Antibiotics Laboratory, Discovery Research Institute, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol052916m

Reference47 articles.

1. The [4 + 4] cycloaddition and its strategic application in natural product synthesis

2. Nickel-catalyzed intramolecular [4 + 4]-cycloadditions: a new method for the synthesis of polycycles containing eight-membered rings

3. Preparation of 2,3-dimethylene-2,3-dihydrofurans by the flash vacuum pyrolysis of substituted furylmethyl esters

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