The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), alpha-methylation, subsequent conversion into the diazoethanone 14, and, finally, treatment with dirhodium tetraacetate of which furnished the hydrindanone 1 of the steroid C-D ring structure.

A New Hydrindanone Synthesis

EPIFANO, Francesco;
2000-01-01

Abstract

The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), alpha-methylation, subsequent conversion into the diazoethanone 14, and, finally, treatment with dirhodium tetraacetate of which furnished the hydrindanone 1 of the steroid C-D ring structure.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/109451
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