Synlett 2013; 24(14): 1818-1824
DOI: 10.1055/s-0033-1339347
letter
© Georg Thieme Verlag Stuttgart · New York

Synthesis of the Cysteine Protease Inhibitors CPI-2081a and CPI-2081b Using a Controlled SPPS Byproduct Forming Reaction

Amanda M. Heapy
a   School of Chemical Sciences, The University of Auckland, 23 Symonds St, Auckland, 1010, New Zealand
b   Centre for Brain Research, The University of Auckland, 85 Park Road, Auckland, 1023, New Zealand
,
Mike Dragunow
b   Centre for Brain Research, The University of Auckland, 85 Park Road, Auckland, 1023, New Zealand
,
Margaret A. Brimble*
a   School of Chemical Sciences, The University of Auckland, 23 Symonds St, Auckland, 1010, New Zealand
b   Centre for Brain Research, The University of Auckland, 85 Park Road, Auckland, 1023, New Zealand
c   School of Biological Sciences, The University of Auckland, 3A Symonds St, Auckland, 1010, New Zealand   Fax: +64(9)3737422   eMail: m.brimble@auckland.ac.nz
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Publikationsverlauf

Received: 16. April 2013

Accepted: 10. Juni 2013

Publikationsdatum:
24. Juli 2013 (online)


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Abstract

An efficient first synthesis of the cysteine protease inhibitors CPI-2081a and CPI-2081b is described. These naturally occurring penta-peptides exhibit extensive amino acid modifications including N-terminal acylation, S-tert-butylation and C-2 ­p-hydroxy­benzyl alkylation of the tryptophan indole ring in CPI-2081b. Both compounds were synthesised by using Fmoc SPPS. In the case of CPI-2081b a SPPS side reaction was optimized to allow straightforward synthetic access to this p-hydroxybenzylated tryptophan-containing natural product.

Supporting Information