Five-Step Total Synthesis of (±)-Aspidospermidine by a Lactam Strategy via an Azomethine Ylide-Reference-Cited by-同舟云学术

Five-Step Total Synthesis of (±)-Aspidospermidine by a Lactam Strategy via an Azomethine Ylide

Author:

Katahara Seiya¹,Sugiyama Yasukazu¹,Yamane Mina¹,Komiya Yukinori¹,Sato Takaaki¹^ORCID,Chida Noritaka¹^ORCID

Affiliation:

1. Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1, Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

Reference90 articles.

1. aSaxton, J. E. In The Alkaloids: Chemistry and Biology; Cordell, G. A., Ed. Academic Press: San Diego, CA, 1998; Vol. 50, pp 343–376.

2. bLopchuk, J. M. In Progress in Heterocyclic Chemistry; Gribble, G. W., Joule, J. A., Eds. Elsevier: Oxford, U.K., 2011; Vol. 23, pp 1–25.

3. aSaxton, J. E. Chemistry of Heterocyclic Compounds; Wiley-Interscience: New York, 1983; Vol. 25, pp 331–437.

4. bSaxton, J. E. In The Alkaloids: Chemistry and Biology; Cordell, G. A., Ed. Academic Press: San Diego, 1998; Vol. 51, pp 1–197.

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