A one-pot diastereoselective synthesis of 1,3-diols and 1,3,5-triols via cascade reactions of arylalkynyl Grignard reagents with enol esters

Author:

Jiao Yinchun123,Zhao Wenjing1,Deng Shuang1,Tang Zilong123,Liu Wanqiang123ORCID,Wan Yichao123,Zhong Fuqi1

Affiliation:

1. School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan, P.R. China

2. Key Laboratory of Theoretical Organic Chemistry and Functional Molecular, Ministry of Education, Hunan University of Science and Technology, Xiangtan, P.R. China

3. Hunan Provincial Key Laboratory of Controllable Preparation and Functional Application of Fine Polymers, Hunan University of Science and Technology, Xiangtan, P.R. China

Abstract

An efficient cascade reaction has been developed to synthesize a series of 1,3-diols and 1,3,5-triols via reactions of arylalkynyl Grignard reagents with enol esters. The stereoselectivity of reactions and the molecular configurations of the products were confirmed by nuclear magnetic resonance, X-ray diffraction, and high-performance liquid chromatography analysis. A possible reaction mechanism was analyzed with the results indicating that it proceeded through a 1,2-addition/rearrangement and reverse O-acylation to produce the 1,3-diol and via C-acylation to form the 1,3,5-triol.

Funder

innovative research group project of the national natural science foundation of china

natural science foundation of hunan province

Publisher

SAGE Publications

Subject

General Chemistry

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