Literature DB >> 21463003

Optically active 1,1'-spirobiindane-7,7'-diol (SPINOL)-based phosphoric acids as highly enantioselective catalysts for asymmetric organocatalysis.

Chun-Hui Xing1, Yuan-Xi Liao, Jaclynn Ng, Qiao-Sheng Hu.   

Abstract

The synthesis and application of a series of optically active 1,1'-spirobiindane-7,7'-diol (SPINOL)-based phosphoric acids are described. These SPINOL-based phosphoric acids were prepared from (R)-SPINOL in three steps and exhibited excellent enantioselectivities for the reactions of indoles with aldimines and β,γ-unsaturated-α-ketoesters. Our study provides a family of promising chiral phosphoric acids to the asymmetric organocatalysis toolbox.

Entities:  

Year:  2011        PMID: 21463003     DOI: 10.1021/jo200302x

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


  3 in total

1.  Selecting Chiral BINOL-Derived Phosphoric Acid Catalysts: General Model To Identify Steric Features Essential for Enantioselectivity.

Authors:  Jolene P Reid; Jonathan M Goodman
Journal:  Chemistry       Date:  2017-09-14       Impact factor: 5.236

2.  Permanent porous hydrogen-bonded frameworks with two types of Brønsted acid sites for heterogeneous asymmetric catalysis.

Authors:  Wei Gong; Dandan Chu; Hong Jiang; Xu Chen; Yong Cui; Yan Liu
Journal:  Nat Commun       Date:  2019-02-05       Impact factor: 14.919

3.  Gold and BINOL-phosphoric acid catalyzed enantioselective hydroamination/N-sulfonyliminium cyclization cascade.

Authors:  Alex W Gregory; Pavol Jakubec; Paul Turner; Darren J Dixon
Journal:  Org Lett       Date:  2013-08-28       Impact factor: 6.005

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.