Difficult Macrocyclizations: New Strategies for Synthesizing Highly Strained Cyclic Tetrapeptides-Reference-Cited by-同舟云学术

Difficult Macrocyclizations: New Strategies for Synthesizing Highly Strained Cyclic Tetrapeptides

Published:2003-07-01 Issue:15 Volume:5 Page:2711-2714
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Meutermans Wim D. F.¹,Bourne Gregory T.¹,Golding Simon W.¹,Horton Douglas A.¹,Campitelli Marc R.¹,Craik David¹,Scanlon Martin¹,Smythe Mark L.¹

Affiliation:

1. Institute for Molecular Bioscience, The University of Queensland, St. Lucia, QLD 4072, Australia, Protagonist Pty. Ltd., Level 1, 11 Lang Parade, Milton, QLD 4064, Australia, and Victorian College of Pharmacy, Monash University, 381 Royal, Parade, Parkville, VIC 3052, Australia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol034907o

Reference27 articles.

1. Conformationally constrained biologically active peptides: tentative identification of the antimitogenic bioactive confomer of the naturally occurring cyclic tetrapeptides

2. Conformational analysis by NMR spectrometry of the highly substituted cyclic tetrapeptides, chlamydocin and Ala4-chlamydocin. Evidence for a unique amide bond sequence in dimethyl sulfoxide-d6

3. Structure of HC-toxin, a cyclic tetrapeptide from helminthosporium carbonum

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