A solution to the component instability problem in the preparation of peptides containing C2-substituted cis-cyclobutane β-aminoacids: synthesis of a stable …
O Roy, S Faure, DJ Aitken
Index: Roy, Olivier; Faure, Sophie; Aitken, David J. Tetrahedron Letters, 2006 , vol. 47, # 33 p. 5981 - 5984
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Citation Number: 33
Abstract
Despite the inherent instability of C2-substituted cis-cyclobutane β-aminoacids, incorporation of such residues into peptides is shown to be possible through use of a 1- amino-2-(hydroxymethyl) cyclobutane derivative as a stable β-aminoacid surrogate. This synthetic strategy was validated by the synthesis of a rhodopeptin analogue.
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