Stereoselective synthesis of the S- and Y-ring systems of maitotoxin

DOI: 10.1248/cpb.44.627

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 627 - 629 (1996)

Update date:2022-08-03

Topics:

Authors:

Nakata Nakata

Nomura Nomura

Matsukura

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Article abstract of DOI:10.1248/cpb.44.627

The seven-membered S- and Y-ring systems of maitotoxin (1) were stereoselectively synthesized based on the rearrangement-ring expansion of the six-membered ethers having the mesylate group on the α-side chain.

Full text of DOI:10.1248/cpb.44.627

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