Literature DB >> 19954140

Efficient synthesis of functionalized aziridinium salts.

Hyun-Soon Chong1, Hyun A Song, Mamta Dadwal, Xiang Sun, Inseok Sin, Yunwei Chen.   

Abstract

Various aziridinium salts were efficiently prepared from bromination of a series of backbone substituted N,N-bisubstituted beta-amino alcohols and isolated via flash column chromatography. The effect of C-substitution, N-substitution, solvent, leaving group, and counteranions on formation of the isolable aziridinium salts was investigated.

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Year:  2010        PMID: 19954140     DOI: 10.1021/jo901893n

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Application of aziridinium ring opening for preparation of optically active diamine and triamine analogues: Highly efficient synthesis and evaluation of DTPA-based MRI contrast enhancement agents.

Authors:  Xiang Sun; Yunwei Chen; Ningjie Wu; Chi Soo Kang; Hyun A Song; Shengnan Jin; Yao Fu; Henry Bryant; Joseph A Frank; Hyun-Soon Chong
Journal:  RSC Adv       Date:  2015-11-03       Impact factor: 3.361

2.  An increase in side-group hydrophobicity largely improves the potency of ritonavir-like inhibitors of CYP3A4.

Authors:  Eric R Samuels; Irina F Sevrioukova
Journal:  Bioorg Med Chem       Date:  2020-01-31       Impact factor: 3.641

  2 in total

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