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Assembly of the isoindolinone core of muironolide A by asymmetric intramolecular Diels-Alder cycloaddition.

ABSTRACT: The hexahydro-1H-isoindolin-1-one core of muironolide A was prepared by asymmetric intramolecular Diels-Alder cycloaddition using a variant of the MacMillan organocatalyst which sets the C4,C5 and C11 stereocenters.

SUBMITTER: Flores B

PROVIDER: S-EPMC4000739 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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Assembly of the isoindolinone core of muironolide A by asymmetric intramolecular Diels-Alder cycloaddition.

Flores Beatris B Molinski Tadeusz F TF

Organic letters 20110713 15

The hexahydro-1H-isoindolin-1-one core of muironolide A was prepared by asymmetric intramolecular Diels-Alder cycloaddition using a variant of the MacMillan organocatalyst which sets the C4,C5 and C11 stereocenters. ...[more]

PMID: 21751773

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