Synthesis of a cyclic urea as a nonnatural biopolymer scaffold
- Authors
- Kim, JM; Wilson, TE; Norman, TC; Schultz, 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
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