CP-225,917 and CP-263,114 synthesis support studies: Testing a radical cyclization strategy for installation of the side-chains.
Author(s)
Banwell, MG
Coster, MJ
Edwards, AJ
Vogtle, M
Griffith University Author(s)
Year published
2003
Metadata
Show full item recordAbstract
The selenocarbonate (I) has been prepd. and shown to react with hexabutyldistannane hydride/allyltributylstannane to give, via a radical cyclization/allylation sequence, the lactone (II) embodying vicinal and trans-related functionality likely to be appropriate for elaboration to the side-chains assocd. with the title compds., a.k.a. phomoidride A and phomoidride B, resp.The selenocarbonate (I) has been prepd. and shown to react with hexabutyldistannane hydride/allyltributylstannane to give, via a radical cyclization/allylation sequence, the lactone (II) embodying vicinal and trans-related functionality likely to be appropriate for elaboration to the side-chains assocd. with the title compds., a.k.a. phomoidride A and phomoidride B, resp.
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Journal Title
Australian Journal of Chemistry
Volume
56
Issue
6
Subject
Chemical sciences