Synthesis of a cyclic urea as a nonnatural biopolymer scaffold

Authors
Kim, JMWilson, TENorman, TCSchultz, PG
Issue Date
1996-07-22
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON LETTERS, v.37, no.30, pp.5309 - 5312
Abstract
A cyclic urea trimer was synthesized from readily available amino acid derivatives using a simple, iterative approach. A selective amide reduction using borane (BH3-THF) and a triphosgens-mediated cyclization are the key features in a synthesis of the cyclic urea trimer 2. Copyright (C) 1996 Elsevier Science Ltd
Keywords
PEPTIDE COMBINATORIAL LIBRARIES; VINYLOGOUS SULFONYL PEPTIDES; SOLID-PHASE SYNTHESIS; UNNATURAL BIOPOLYMERS; DRUG DISCOVERY; PEPTIDE COMBINATORIAL LIBRARIES; VINYLOGOUS SULFONYL PEPTIDES; SOLID-PHASE SYNTHESIS; UNNATURAL BIOPOLYMERS; DRUG DISCOVERY
ISSN
0040-4039
URI
https://pubs.kist.re.kr/handle/201004/144382
DOI
10.1016/0040-4039(96)01101-X
Appears in Collections:
KIST Article > Others
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE