An enantiospecific synthesis of the tricyclic guanidine segment of the anti-HIV marine alkaloid batzelladine A

Rama Rao, A. V. ; Gurjar, Mukund K. ; Vasudevan, Jayasree (1995) An enantiospecific synthesis of the tricyclic guanidine segment of the anti-HIV marine alkaloid batzelladine A Journal of the Chemical Society, Chemical Communications (13). pp. 1369-1370. ISSN 0022-4936

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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/1995...

Related URL: http://dx.doi.org/10.1039/C39950001369

Abstract

An enantiospecific synthesis of the tricyclic guanidine segment 19 of the new anti-HIV alkaloid batzelladine A, isolated from a marine sponge of genus batzella, starting from [3R(1'R,4R)]-4-acetoxy-3-[1-(ferf-butyldimethylsilyloxy)ethyl]-2-azetidinone 3 is described.

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