Literature DB >> 11506621

The application of chiral aminonaphthols in the enantioselective addition of diethylzinc to aryl aldehydes.

D X Liu1, L C Zhang, Q Wang, C S Da, Z Q Xin, R Wang, M C Choi, A S Chan.   

Abstract

[reaction: see text]. Optically active aminonaphthol 3 obtained by condensation of 2-naphthol, benzaldehyde, and (S)-methylbenzylamine followed by N-methylation was found to catalyze the enantioselective ethylation of aryl aldehydes to secondary alcohols with high enantioselectivities (up to 99.8%) at room temperature.

Entities:  

Year:  2001        PMID: 11506621     DOI: 10.1021/ol016341e

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


  2 in total

1.  1-{Phen-yl[1-(p-tol-yl)ethyl-amino]meth-yl}-2-naphthol.

Authors:  Yong Hua Li; Min Min Zhao; Yuan Zhang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-09-24

Review 2.  Recent advances in the synthesis and synthetic applications of Betti base (aminoalkylnaphthol) and bis-Betti base derivatives.

Authors:  Abolfazl Olyaei; Mahdieh Sadeghpour
Journal:  RSC Adv       Date:  2019-06-11       Impact factor: 4.036

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.