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High yield synthesis of tentoxin, a cyclic tetrapeptide
Author(s) -
Loiseau Nicolas,
Cavelier Florine,
Noel JeanPierre,
Gomis JeanMarie
Publication year - 2002
Publication title -
journal of peptide science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 66
eISSN - 1099-1387
pISSN - 1075-2617
DOI - 10.1002/psc.393
Subject(s) - tetrapeptide , chemistry , yield (engineering) , reagent , cyclic peptide , stereochemistry , total synthesis , amino acid , combinatorial chemistry , organic chemistry , peptide , biochemistry , materials science , metallurgy
Abstract Tentoxin is a naturally occurring phytotoxic cyclic tetrapeptide excreted by fungi of the Alternaria alternata family. The four total syntheses of tentoxin published to date give poor total yields, mainly owing to two difficulties, the introduction of the dehydro amino acid and more especially the cyclization step. Here we describe a method that stereospecifically introduces Z‐dehydrophenylalanine (Δ Z Phe) by a modified Erlenmeyer aldolization reaction. The linear tetrapeptide, Boc‐R 1 Ala‐Leu‐R 2 Δ Z Phe‐Gly‐OMe (R 1 , R 2 : CH 3 , 14 CH 3 ), the precursor of tentoxin, was obtained in a 72% yield from Boc‐Leu‐Gly‐OH. This linear tetrapeptide, labelled with carbon‐14, was used for a comparative study of four cyclization reagents DPPA, DCC–PfpOH, HBTU and HATU. This last was the most effective and gave tentoxin in a 81% cyclization yield. The activated ester formed with this reagent displayed an enhanced capacity for cyclization, permitting cyclization in concentrated medium (10 m M ). This new synthetic route gave tentoxin in a 60% yield from Boc‐Leu‐Gly‐OH and offers a means of achieving the synthesis of hitherto elusive analogues. Copyright © 2002 European Peptide Society and John Wiley & Sons, Ltd.