| Literature DB >> 16928100 |
Takayuki Doi1, Masahito Yoshida, Kazuo Shin-ya, Takashi Takahashi.
Abstract
We have achieved a total synthesis of telomestatin, and its absolute configuration was determined to be (R). Coupling of cysteine-containing trisoxazole amine and serine-containing trisoxazole carboxylic acid, followed by macrocyclization, provided a 24-membered diamide. The seventh oxazole ring was formed by a Shin's procedure via dehydroamide. Cyclodehydration of a modified (R)-cysteine-(S-(t)Bu) moiety using Kelly's method (PPh3(O)-Tf2O) with anisole furnished (R)-telomestatin, whose CD spectrum was in good agreement with that of the natural product.Entities:
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Year: 2006 PMID: 16928100 DOI: 10.1021/ol061793i
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005