A Computationally Designed Rh(I)-Catalyzed Two-Component [5+2+1] Cycloaddition of Ene-vinylcyclopropanes and CO for the Synthesis of Cyclooctenones-Reference-Cited by-同舟云学术

A Computationally Designed Rh(I)-Catalyzed Two-Component [5+2+1] Cycloaddition of Ene-vinylcyclopropanes and CO for the Synthesis of Cyclooctenones

Published:2007-07-27 Issue:33 Volume:129 Page:10060-10061
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wang Yuanyuan¹,Wang Jingxin¹,Su Jiachun¹,Huang Feng¹,Jiao Lei¹,Liang Yong¹,Yang Dazhi¹,Zhang Shiwei¹,Wender Paul A.¹,Yu Zhi-Xiang¹

Affiliation:

1. Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China, and Departments of Chemistry and of Chemical and Systems Biology, Stanford University, Stanford, California 94305-5080

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja072505w

Reference26 articles.

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2. Selective Construction of Carbocyclic Eight-Membered Rings by Ring-Closing Metathesis of Acyclic Precursors

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

4. Progress in the Construction of Cyclooctanoid Systems: New Approaches and Applications to Natural Product Syntheses

5. (e) Wender, P. A.; Croatt, M. P.; Deschamps, N. M. inComprehensiveOrganometallic Chemistry III; Ojima, I., Ed.; Elsevier Ltd: 2007; Vol. 10, pp 603−648.

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