Arylation of Phe and Tyr Side Chains of Unprotected Peptides by a Suzuki−Miyaura Reaction in Water-Reference-Cited by-同舟云学术

Arylation of Phe and Tyr Side Chains of Unprotected Peptides by a Suzuki−Miyaura Reaction in Water

Published:2008-07-04 Issue:15 Volume:10 Page:3243-3245
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Vilaró Maria¹,Arsequell Gemma¹,Valencia Gregorio¹,Ballesteros Alfredo¹,Barluenga José¹

Affiliation:

1. Instituto de Investigacions Quimicas y Ambientales de Barcelona, Jordi Girona 18-26 E08034, Barcelona, Spain, and Instituto Universitario de Química Organometálica “Enrique Moles” Unidad Asociada al C.S.I.C., Universidad de Oviedo, Julián Clavería, 8; 33006 Oviedo, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol801009z

Reference38 articles.

1. Peptides: Chemistry and Biology

2. A Versatile Tandem Catalysis Procedure for the Preparation of Novel Amino Acids and Peptides

3. Dicarba Analogues of the Cyclic Enkephalin Peptides H-Tyr-c[d-Cys-Gly-Phe-d(or l)-Cys]NH2 Retain High Opioid Activity

4. Structure−Activity Relationships of Bifunctional Peptides Based on Overlapping Pharmacophores at Opioid and Cholecystokinin Receptors

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