Transannular Diels–Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Total Synthesis of a Unique Set of Vinblastine Analogues-Reference-Cited by-同舟云学术

Transannular Diels–Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Total Synthesis of a Unique Set of Vinblastine Analogues

Published:2013-10-02 Issue:20 Volume:15 Page:5306-5309
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Campbell Erica L.¹,Skepper Colin K.¹,Sankar Kuppusamy¹,Duncan Katharine K.¹,Boger Dale L.¹

Affiliation:

1. Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States

Funder

National Institutes of Health

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol402549n

Reference49 articles.

1. Neuss, N.; Neuss, M. N.InThe Alkaloids;Brossi, A., Suffness, M., Eds.Academic:San Diego, 1990; Vol.37, p229.

2. ROLE OF CHANCE OBSERVATIONS IN CHEMOTHERAPY:VINCA ROSEA*

3. Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.) V.**Organic Chemical Development and Lilly Research Laboratories, Eli Lilly and Co., Indianapolis, Ind.

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