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Synthesis of brevetoxin sub-units by sequential ring-closing metathesis and hydroboration

✍ Scribed by J Stephen^Clark; Jason G Kettle

Publisher: Elsevier Science
Year: 1997
Tongue: French
Weight: 237 KB
Volume: 38
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(96)02232-0

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✦ Synopsis

A new strategy for the construction of polycyclic ethers by sequential ring-closing metathesis and stereoselective hydroboration has been explored. This sequence of reactions has been used to prepare bicyclic ethers corresponding to sub-units of brevetoxin B.

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## Abstract For Abstract see ChemInform Abstract in Full Text.