Enantioselective synthesis of indanone spiro-isochromanone derivatives via a dinuclear zinc-catalyzed Michael/transesterification tandem reaction-Reference-Cited by-同舟云学术

Enantioselective synthesis of indanone spiro-isochromanone derivatives via a dinuclear zinc-catalyzed Michael/transesterification tandem reaction

Published:2020 Issue:20 Volume:18 Page:3917-3926
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yang Xiao-Chao¹²³⁴,Xu Meng¹²³⁴,Wang Jin-Bao¹²³⁴,Liu Meng-Meng¹²³⁴,Mathey François¹²³⁴^ORCID,Hua Yuan-Zhao¹²³⁴,Wang Min-Can¹²³⁴^ORCID

Affiliation:

1. College of Chemistry and Institute of Green catalysis

2. Zhengzhou University

3. Zhengzhou

4. P. R. China

Abstract

A series of enantiomerically pure indanone spiro-isochromanones are obtained via a dinuclear zinc catalyzed asymmetric tandem Michael addition/transesterification reaction of α-hydroxy indanones with ortho-ester chalcones.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00541J

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