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Enantioselective total synthesis of polyoxygenated cyclohexanoids: (+)-streptol, ent-RKTS-33 and putative ‘(+)-parasitenone’. Identity of parasitenone with (+)-epoxydon by Goverdhan Mehta; Shashikant R. Pujar; Senaiar S. Ramesh; Kabirul Islam is a Chemistry article available to read on EtoBox.

What is Enantioselective total synthesis of polyoxygenated cyclohexanoids: (+)-streptol, ent-RKTS-33 and putative ‘(+)-parasitenone’. Identity of parasitenone with (+)-epoxydon about?

Short, simple and enantioselective syntheses of the natural product (+)-streptol, the non-peptide apoptosis inhibitor ent-RKTS-33 and the putative structure of ÔparasitenoneÕ have been accomplished from the readily available chiral building block. ÔParasitenoneÕ has been shown to be identical with the known natural product epoxydon.

Who reads Enantioselective total synthesis of polyoxygenated cyclohexanoids: (+)-streptol, ent-RKTS-33 and putative ‘(+)-parasitenone’. Identity of parasitenone with (+)-epoxydon?

Author

Goverdhan Mehta; Shashikant R. Pujar; Senaiar S. Ramesh; Kabirul Islam

Publisher

Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4039)

Published

2005

Language

EN

Field

Chemistry (Physical Sciences)