Literature DB >> 22452360

4-Methoxybenzyloxymethyl group, a racemization-resistant protecting group for cysteine in Fmoc solid phase peptide synthesis.

Hajime Hibino1, Yuji Nishiuchi.   

Abstract

The 4-methoxybenzyloxymethyl (MBom) group was introduced for sulfhydryl protection of Cys in combination with Fmoc chemistry. The MBom group proved to substantially suppress racemization of Cys during its incorporation mediated by phosphonium or uronium reagents. Furthermore, this group was found to significantly reduce racemization of the C-terminal Cys linked to a hydroxyl resin during repetitive base treatment, in comparison with the usually used trityl (Trt) and acetamidomethyl (Acm) groups.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22452360     DOI: 10.1021/ol300592w

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  8 in total

1.  Malaria-infected mice live until at least day 30 after a new artemisinin-derived thioacetal thiocarbonate combined with mefloquine are administered together in a single, low, oral dose.

Authors:  Alexander M Jacobine; Jennifer R Mazzone; Rachel D Slack; Abhai K Tripathi; David J Sullivan; Gary H Posner
Journal:  J Med Chem       Date:  2012-08-27       Impact factor: 7.446

2.  Facile removal of 4-methoxybenzyl protecting group from selenocysteine.

Authors:  Kaelyn A Jenny; Emma J Ste Marie; Gracyn Mose; Erik L Ruggles; Robert J Hondal
Journal:  J Pept Sci       Date:  2019-08-13       Impact factor: 1.905

3.  Carbodiimide-Mediated Beckmann Rearrangement of Oxyma-B as a Side Reaction in Peptide Synthesis.

Authors:  Andrea Orlandin; Ivan Guryanov; Lucia Ferrazzano; Barbara Biondi; Francesca Biscaglia; Claudia Storti; Marzio Rancan; Fernando Formaggio; Antonio Ricci; Walter Cabri
Journal:  Molecules       Date:  2022-06-30       Impact factor: 4.927

Review 4.  Recent advances in the synthesis of C-terminally modified peptides.

Authors:  Christine A Arbour; Lawrence G Mendoza; Jennifer L Stockdill
Journal:  Org Biomol Chem       Date:  2020-09-30       Impact factor: 3.890

5.  Evaluation of acid-labile S-protecting groups to prevent Cys racemization in Fmoc solid-phase peptide synthesis.

Authors:  Hajime Hibino; Yasuyoshi Miki; Yuji Nishiuchi
Journal:  J Pept Sci       Date:  2013-11-28       Impact factor: 1.905

Review 6.  Understanding Tetrahydropyranyl as a Protecting Group in Peptide Chemistry.

Authors:  Anamika Sharma; Iván Ramos-Tomillero; Ayman El-Faham; Ernesto Nicolas; Hortensia Rodriguez; Beatriz G de la Torre; Fernando Albericio
Journal:  ChemistryOpen       Date:  2017-03-08       Impact factor: 2.911

7.  Epimerization-free access to C-terminal cysteine peptide acids, carboxamides, secondary amides, and esters via complimentary strategies.

Authors:  Christine A Arbour; Thilini D Kondasinghe; Hasina Y Saraha; Teanna L Vorlicek; Jennifer L Stockdill
Journal:  Chem Sci       Date:  2017-11-09       Impact factor: 9.825

Review 8.  Chemical synthesis, backbone cyclization and oxidative folding of cystine-knot peptides: promising scaffolds for applications in drug design.

Authors:  Michael Reinwarth; Daichi Nasu; Harald Kolmar; Olga Avrutina
Journal:  Molecules       Date:  2012-10-24       Impact factor: 4.411

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.