Literature DB >> 20830335

Efficient and chemoselective alkylation of amines/amino acids using alcohols as alkylating reagents under mild conditions.

Chu-Pei Xu1, Zhen-Hua Xiao, Bi-Qin Zhuo, Yu-Huang Wang, Pei-Qiang Huang.   

Abstract

We report a mild and environmentally benign method for the synthesis of tertiary amines using alcohols as the alkylating reagents. Not only secondary amines such as piperazines but also amino acids and amino alcohols can be N-alkylated selectively. For N,O-benzyl protected amino alcohols, both N,O-de-benzylation and N-methylation were achieved in one-pot.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20830335     DOI: 10.1039/c0cc01487g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

1.  Obstacles and solutions for chemical synthesis of syndecan-3 (53-62) glycopeptides with two heparan sulfate chains.

Authors:  Weizhun Yang; Keisuke Yoshida; Bo Yang; Xuefei Huang
Journal:  Carbohydr Res       Date:  2016-10-20       Impact factor: 2.104

2.  Ph3P/CCl4 as a highly efficient reagent for one-pot N-alkylation of sulfonamides from alcohols: a rapid route to N-alkyl sulfonamides synthesis.

Authors:  Mohammad Navid Soltani Rad; Somayeh Behrouz
Journal:  Mol Divers       Date:  2013-08-14       Impact factor: 2.943

3.  Direct N-alkylation of unprotected amino acids with alcohols.

Authors:  Tao Yan; Ben L Feringa; Katalin Barta
Journal:  Sci Adv       Date:  2017-12-08       Impact factor: 14.136

4.  Efficient and selective N-alkylation of amines with alcohols catalysed by manganese pincer complexes.

Authors:  Saravanakumar Elangovan; Jacob Neumann; Jean-Baptiste Sortais; Kathrin Junge; Christophe Darcel; Matthias Beller
Journal:  Nat Commun       Date:  2016-10-06       Impact factor: 14.919

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.