Construction of the tetracyclic ring system of diterpene alkaloids via cationic [5 + 2] cycloaddition

Author:

Mizuno Kosuke1,Nishiyama Yoshitake1,Yokoshima Satoshi1ORCID

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Nagoya University, Nagoya 464-8601, Japan

Abstract

The ABCD ring system of C18/C19 diterpene alkaloids was constructed via cationic [5 + 2] cycloaddition and an intramolecular aldol reaction.

Funder

Japan Agency for Medical Research and Development

Naito Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference38 articles.

1. F.-P.Wang , Q.-H.Chen and X.-T.Liang , in The Alkaloids: Chemistry and Biology , ed. G. A. Cordell , Academic Press , 2009 , vol. 67 , p. 1

2. F.-P.Wang and Q.-H.Chen , in The Alkaloids: Chemistry and Biology , ed. G. A. Cordell , Academic Press , 2010 , vol. 69 , p. 1

3. X.-Y.Liu , B.-W.Ke , Y.Qin and F.-P.Wang , in The Alkaloids: Chemistry and Biology , ed. H.-J. Knölker , Academic Press , 2022 , vol. 87 , p. 1

4. Total synthesis of talatisamine, a delphinine type alkaloid

5. A new stereospecific total synthesis of chasmanine and 13-desoxydelphonine

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