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A Domino 10-Step Total Synthesis of FR252921 and Its Analogues, Complex Macrocyclic Immunosuppressants
Author(s) -
Yong Chen,
Guilhem Coussanes,
Caroline Souris,
Paul Aillard,
Dainis Kaldre,
Kathrin Runggatscher,
Stefan Kubicek,
Giovanni Di Mauro,
Boris Maryasin,
Nuno Maulide
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b07185
Subject(s) - chemistry , domino , moiety , polyene , stereoselectivity , stereochemistry , total synthesis , combinatorial chemistry , ring (chemistry) , organic chemistry , catalysis
FR252921, FR252922, and FR256523 are a family of potent macrocyclic polyene immunosuppressive agents with a novel mode of action. However, the lack of an efficient and flexible synthesis has hindered further biological studies, mostly due to the fact that the natural products appear to be kinetic isomers regarding the triene moiety. Herein, we report the development and application of an unprecedented, unique domino Suzuki-Miyaura/4π-electrocyclic ring-opening macrocyclization, resulting in a concise, unified, and stereoselective synthetic route to these complex targets in only 10 steps. This in turn enables ready access to a range of unnatural analogues, among which several compounds showed inhibition of T-lymphocyte proliferation at levels equal or superior to those of the natural products themselves.

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