Literature DB >> 34358424

SPHENOL, A New Chiral Framework for Asymmetric Synthesis.

Ronghua Zhang1, Shulin Ge1, Jianwei Sun1,2.   

Abstract

Privileged chiral catalysts have found tremendous applications and thus immensely advanced asymmetric synthesis in the past few decades. However, truly privileged chiral frameworks are still extremely limited. Thus, the search for and development of new versatile members remain in high demand but challenging. Herein we report the design, synthesis, and application of a new chiral framework, SPHENOL, which features combined advantages of BINOL and SPINOL. This unique feature enables SPHENOL to serve as a new platform for the development of chiral ligands and catalysts. Its superior performance has been demonstrated in mechanistically unrelated reactions, including asymmetric hydrogenation, hydroacylation, and spirocyclization for the practical asymmetric synthesis of SPHENOL itself. These results indicated the great potential of SPHENOL as a useful chiral framework.

Entities:  

Year:  2021        PMID: 34358424     DOI: 10.1021/jacs.1c05709

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Optical resolution of 1,16-dihydroxytetraphenylene by chiral gold(iii) complexation and its applications as chiral ligands in asymmetric catalysis.

Authors:  Jia Guo; Wen-Bin Xiong; Hao-Ran Ma; Luoyi Fan; You-Yun Zhou; Henry N C Wong; Jian-Fang Cui
Journal:  Chem Sci       Date:  2022-03-24       Impact factor: 9.969

2.  Stereoselective Synthesis of Atropisomeric Acridinium Salts by the Catalyst-Controlled Cyclization of ortho-Quinone Methide Iminiums.

Authors:  Xingxing Wu; Christof Sparr
Journal:  Angew Chem Int Ed Engl       Date:  2022-02-25       Impact factor: 16.823

  2 in total

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