Literature DB >> 1421811

4-Methyltrityl (Mtt): a new protecting group for the side chain protection of Asn and Gln in solid-phase peptide synthesis.

B Sax1, F Dick, R Tanner, J Gosteli.   

Abstract

The trityl group was recently introduced for the protection of the side chain carboxamide function of asparagine and glutamine. The 4-methyltrityl (Mtt) group, a structural modification of trityl, is presented here and allows more rapid cleavage from the protected peptides. Procedures for the introduction of the group and comparative cleavage reactions are also presented.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1421811

Source DB:  PubMed          Journal:  Pept Res        ISSN: 1040-5704


  3 in total

1.  Facile Semisynthesis of Ubiquitylated Peptides with the Ligation Auxiliary 2-Aminooxyethanethiol.

Authors:  Caroline E Weller; Champak Chatterjee
Journal:  Methods Mol Biol       Date:  2020

2.  Facile synthesis of native and protease-resistant ubiquitylated peptides.

Authors:  Caroline E Weller; Wei Huang; Champak Chatterjee
Journal:  Chembiochem       Date:  2014-05-18       Impact factor: 3.164

3.  Understanding acid lability of cysteine protecting groups.

Authors:  Iván Ramos-Tomillero; Lorena Mendive-Tapia; Miriam Góngora-Benítez; Ernesto Nicolás; Judit Tulla-Puche; Fernando Albericio
Journal:  Molecules       Date:  2013-05-06       Impact factor: 4.411

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.