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Synthesis of the tetracyclic core of the neomangicols using a late-stage indene alkylation.

ABSTRACT: A general approach to the tetracyclic core of the neomangicol natural products via a late-stage indene alkylation reaction is presented. This strategy sets the stage for access to the neomangicol family and, in addition, provides a potential biogenetically inspired entry to the mangicol natural products.

SUBMITTER: Wood JL

PROVIDER: S-EPMC2720047 | biostudies-literature | 2009 Jul

REPOSITORIES: biostudies-literature

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Synthesis of the tetracyclic core of the neomangicols using a late-stage indene alkylation.

Wood Jessica L JL Pujanauski Brian G BG Sarpong Richmond R

Organic letters 20090701 14

A general approach to the tetracyclic core of the neomangicol natural products via a late-stage indene alkylation reaction is presented. This strategy sets the stage for access to the neomangicol family and, in addition, provides a potential biogenetically inspired entry to the mangicol natural products. ...[more]

PMID: 19527042

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