Literature DB >> 17117685

Emerging methods in amide- and peptide-bond formation.

Jeffery W Bode1.   

Abstract

Amide bonds are the key chemical connections in proteins and peptides and have a long-established presence in small-molecule therapeutics. Despite their recognized importance, amide bond synthesis relies almost solely on variants of a single reaction: the dehydrative coupling of carboxylic acids and amines. While phenomenally successful in many applications, this process requires superstoichiometric quantities of expensive reagents and precludes chemoselective ligation reactions. This review summarizes emerging chemical alternatives to amide-bond formation with particular emphasis on the development of ligation reactions that permit the coupling of unprotected peptide fragments.

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Year:  2006        PMID: 17117685

Source DB:  PubMed          Journal:  Curr Opin Drug Discov Devel        ISSN: 1367-6733


  23 in total

1.  Facile amide formation via S-nitrosothioacids.

Authors:  Jia Pan; Nelmi O Devarie-Baez; Ming Xian
Journal:  Org Lett       Date:  2011-01-27       Impact factor: 6.005

2.  A peptide derived from endostatin ameliorates organ fibrosis.

Authors:  Yukie Yamaguchi; Takahisa Takihara; Roger A Chambers; Kristen L Veraldi; Adriana T Larregina; Carol A Feghali-Bostwick
Journal:  Sci Transl Med       Date:  2012-05-30       Impact factor: 17.956

3.  Intramolecular and Intermolecular Schmidt Reactions of Alkyl Azides with Aldehydes.

Authors:  Huey-Lih Lee; Jeffrey Aubé
Journal:  Tetrahedron       Date:  2007-09-03       Impact factor: 2.457

4.  Discovery of competing anaerobic and aerobic pathways in umpolung amide synthesis allows for site-selective amide 18O-labeling.

Authors:  Jessica P Shackleford; Bo Shen; Jeffrey N Johnston
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-19       Impact factor: 11.205

5.  Umpolung reactivity in amide and peptide synthesis.

Authors:  Bo Shen; Dawn M Makley; Jeffrey N Johnston
Journal:  Nature       Date:  2010-06-24       Impact factor: 49.962

6.  Reaction of thioacids with isocyanates and isothiocyanates: a convenient amide ligation process.

Authors:  David Crich; Kaname Sasaki
Journal:  Org Lett       Date:  2009-08-06       Impact factor: 6.005

7.  Thio FCMA intermediates as strong acyl donors: a general solution to the formation of complex amide bonds.

Authors:  Yu Rao; Xuechen Li; Samuel J Danishefsky
Journal:  J Am Chem Soc       Date:  2009-09-16       Impact factor: 15.419

8.  Catalytic amide formation with alpha'-hydroxyenones as acylating reagents.

Authors:  Pei-Chen Chiang; Yoonjoo Kim; Jeffrey W Bode
Journal:  Chem Commun (Camb)       Date:  2009-07-06       Impact factor: 6.222

9.  Triblock peptide and peptide thioester synthesis with reactivity-differentiated sulfonamides and peptidyl thioacids.

Authors:  David Crich; Indrajeet Sharma
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

10.  Dechalcogenative allylic selenosulfide and disulfide rearrangements: complementary methods for the formation of allylic sulfides in the absence of electrophiles. Scope, limitations, and application to the functionalization of unprotected peptides in aqueous media.

Authors:  David Crich; Venkataramanan Krishnamurthy; Franck Brebion; Maheswaran Karatholuvhu; Venkataraman Subramanian; Thomas K Hutton
Journal:  J Am Chem Soc       Date:  2007-07-27       Impact factor: 15.419

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