Synthesis of Peptides and Pseudopeptides Incorporating an endo-(2S,3R)-Norborn-5-ene Residue as a Turn Inducer-Reference-Cited by-同舟云学术

Synthesis of Peptides and Pseudopeptides Incorporating an endo-(2S,3R)-Norborn-5-ene Residue as a Turn Inducer

Published:1998-02-18 Issue:5 Volume:63 Page:1496-1504
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hibbs David E.¹,Hursthouse Michael B.¹,Jones Iwan G.¹,Jones Wyn¹,Abdul Malik K. M.¹,North Michael¹

Affiliation:

1. Department of Chemistry, University of Wales, Bangor, Gwynedd LL57 2UW, U.K. Peboc Division of Eastman Chemical (UK) Ltd., Industrial Estate, Llangefni, Anglesey, Gwynedd LL77 7YQ, U.K., and Department of Chemistry, University of Wales, Cardiff, P.O. Box 912, Park Place, Cardiff CF1 3TB, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9717651

Reference32 articles.

1. Studies of N-terminal templates for .alpha.-helix formation. Synthesis and conformational analysis of peptide conjugates of (2S,5S,8S,11S)-1-acetyl-1,4-diaza-3-keto-5-carboxy-10-thiatricyclo[2.8.1.04,8]tridecane (Ac-Hel1-OH)

2. Hydrophobic Cluster Formation Is Necessary for Dibenzofuran-Based Amino Acids to Function as .beta.-Sheet Nucleators

3. De Novo Design, Synthesis, and X-ray Crystal Structures of Pyrrolinone-Based .beta.-Strand Peptidomimetics

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