Molecules structurally analogous to dipeptides, containing an oxirane ring in the place of the peptidic bond, can be prepared by oxidative conversion of beta-hydroxyselenides obtained by Mukaiyama aldol type reaction of N-protected beta-amino alpha-selenyl aldehydes derived from naturally occurring amino acids. Copyright (C) 1996 Elsevier Science Ltd
Mann, A., Quaranta, L., Reginato, G., Taddei, M. (1996). A general synthesis of oligopeptides containing an oxirane ring in the place of a peptidic bond. TETRAHEDRON LETTERS, 37(15), 2651-2654 [10.1016/0040-4039(96)00352-8].
A general synthesis of oligopeptides containing an oxirane ring in the place of a peptidic bond
Taddei, Maurizio
1996-01-01
Abstract
Molecules structurally analogous to dipeptides, containing an oxirane ring in the place of the peptidic bond, can be prepared by oxidative conversion of beta-hydroxyselenides obtained by Mukaiyama aldol type reaction of N-protected beta-amino alpha-selenyl aldehydes derived from naturally occurring amino acids. Copyright (C) 1996 Elsevier Science Ltd
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https://hdl.handle.net/11365/31387
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