Convenient Synthesis of 3,4-methano-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acid and Its Derivatives as Doubly Constrained Nonproteinogenic Amino Acid Derivatives-Reference-Cited by-同舟云学术

Convenient Synthesis of 3,4-methano-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acid and Its Derivatives as Doubly Constrained Nonproteinogenic Amino Acid Derivatives

Published:2000-08-10 Issue:18 Volume:65 Page:5469-5475
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Czombos József¹,Aelterman Wim¹,Tkachev Alexey¹,Martins José C.¹,Tourwé Dirk¹,Péter Antal¹,Tóth Géza¹,Fülöp Ferenc¹,De Kimpe Norbert¹

Affiliation:

1. Department of Organic Chemistry, Faculty of Agricultural and Applied Biological Sciences, University of Gent, Coupure Links 653, B-9000 Gent, Belgium, Novosibirsk Institute of Organic Chemistry, Novosibirsk, 630090 Russia, HNMR Center (HNMR) and Laboratory of Organic Chemistry (ORGC), Free University of Brussels, Pleinlaan 2, B-1050 Brussels, Belgium, Department of Inorganic and Analytical Chemistry, University of Szeged, P.O. Box 440, H-6701 Szeged, Hungary, Biological Research Center, Hungarian Academy...

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9917994

Reference34 articles.

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2. Conformational restriction of the phenylalanine residue in a cyclic opioid peptide analog: effects on receptor selectivity and stereospecificity

3. Conformational restriction of Tyr and Phe side chains in opioid peptides: Information about preferred and bioactive side‐chain topology

4. Book Reviews

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