Synfacts 2020; 16(03): 0351
DOI: 10.1055/s-0039-1691664
Peptide Chemistry
© Georg Thieme Verlag Stuttgart · New York

Cyclic Peptides Synthesis with the Assistance of a Removable Activating Group

Contributor(s):
Hisashi Yamamoto
,
An Wu
Ben-Lulu M, Gaster E, Libman A, Pappo D. * Ben-Gurion University of the Negev, Beer Sheva, Israel
Synthesis of Biaryl-Bridged Cyclic Peptides via Catalytic Oxidative Cross-Coupling Reactions.

Angew. Chem. Int. Ed. 2020;
Further Information

Publication History

Publication Date:
18 February 2020 (online)

 

Significance

Biaryl-bridged cyclic peptides are becoming more and more important due to their biological activity. The authors have developed an efficient strategy to synthesize these peptides by introducing a removable activating group to increase reactivity in the oxidative cross-coupling step that forms the biaryl unit.


#

Comment

Although the authors have prepared some natural and nonnatural biaryl-bridged cyclic peptides in moderate total yields, this approach with a remarkable activating group (t-Bu) might have more synthetic uses.


#
#