Second approach to the construction of a pentacyclic ring system for neosurugatoxin

DOI: 10.1248/cpb.40.1110

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1110 - 1115 (1992)

Update date:2022-08-04

Topics:

Authors:

Okada Okada

Mizuno Mizuno

Tanino Tanino

Kakoi Kakoi

Inoue Inoue

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Article abstract of DOI:10.1248/cpb.40.1110

The Diels-Alder adduct obtained from (E)-6-bromo-3-ethoxycarbonylmethylene-2-oxoindoline and trans-1,3-pentadiene was successfully transformed into the diacetate of the aglycone of neosurugatoxin, which is the key intermediate in our first total synthesis

Full text of DOI:10.1248/cpb.40.1110

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