Showing papers by "Ernest Wenkert published in 2000"
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TL;DR: The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), α-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 as discussed by the authors.
Abstract: The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), α-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.
6 citations
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TL;DR: The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), α-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.
Abstract: The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), α-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.