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Stereoselective synthesis of a model C(18)-C(35) spiroketal fragment of integramycin.

ABSTRACT: A highly stereoselective synthesis of a model C(18)-C(35) spiroketal unit (7) of integramycin has been accomplished via an enantioselective stannyl-crotylboration reaction and an N-iodosuccinimide-mediated spiroketalization of 19a.

SUBMITTER: Sun H

PROVIDER: S-EPMC3094501 | biostudies-literature | 2011 May

REPOSITORIES: biostudies-literature

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Stereoselective synthesis of a model C(18)-C(35) spiroketal fragment of integramycin.

Sun Huikai H Abbott Jason R JR Roush William R WR

Organic letters 20110421 10

A highly stereoselective synthesis of a model C(18)-C(35) spiroketal unit (7) of integramycin has been accomplished via an enantioselective stannyl-crotylboration reaction and an N-iodosuccinimide-mediated spiroketalization of 19a. ...[more]

PMID: 21510632

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