SNAr-based cycloetherification methodology: application in the synthesis of heterodectic macrocyclic peptides with endo aryl-aryl and aryl-alkyl ether bonds
A review with 42 refs. on the synthesis of heterodectic macrocyclic peptides, focusing on ring closure by formation of aryl-aryl and aryl-alkyl ether bonds via the intramol. SNAr reaction. [on SciFinder (R)]
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Zhu, J. (1999). SNAr-based cycloetherification methodology: application in the synthesis of heterodectic macrocyclic peptides with endo aryl-aryl and aryl-alkyl ether bonds. In Peptidomimetics Protocols (pp. 293–320). https://doi.org/10.1385/0-89603-517-4:293
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1999
0-89603-517-4
293
320
Methods in Molecular Medicine; 23
CAN 132:334735
34-0
Amino Acids, Peptides, and Proteins
Institute de Chimie des Substances Naturelles, CNRS,Gif-sur-Yvette,Fr.
REVIEWED
OTHER