Asymmetric [4 + 3] Cycloadditions between Vinylcarbenoids and Dienes: Application to the Total Synthesis of the Natural Product (−)-5-epi-Vibsanin E-Reference-Cited by-同舟云学术

Asymmetric [4 + 3] Cycloadditions between Vinylcarbenoids and Dienes: Application to the Total Synthesis of the Natural Product (−)-5-epi-Vibsanin E

Published:2009-05-15 Issue:23 Volume:131 Page:8329-8332
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Schwartz Brett D.¹,Denton Justin R.¹,Lian Yajing¹,Davies Huw M. L.¹,Williams Craig M.¹

Affiliation:

1. School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane 4072, Queensland, Australia, Department of Chemistry, University at Buffalo, The State University of New York, Buffalo, New York 14260-3000, and Department of Chemistry, Emory University, 1515 Dickey Drive, Atlanta, Georgia 30322

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9019484

Reference36 articles.

1. aKawazu, K.In11th International Symposium on Chemistry of Natural Products;Golden Sands, Bulgaria, Sept 17−23, 1978;International Union of Pure and Applied Chemistry:Research Park Triangle, NC, 1978; Vol. 2, p101.

2. Structure and absolute configuration of vibsanine E isolated from leaves of Viburnum odoratissimum Ker

3. Seven-Membered Vibsane-Type Diterpenes with a 5,10-cis Relationship from Viburnum awabuki.

4. Expedient Construction of the Vibsanin E Core without the Use of Protecting Groups

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