An Efficient Ecofriendly Enantioselective Organocatalytic Ring-Closing Reaction of 2-Hydroxychalcone via Intramolecular Oxa-Michael Reaction-Reference-Cited by-同舟云学术

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An Efficient Ecofriendly Enantioselective Organocatalytic Ring-Closing Reaction of 2-Hydroxychalcone via Intramolecular Oxa-Michael Reaction

Published:2017-12-01 Issue:34 Volume:2 Page:11160-11163
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Singh Ashawani Kumar¹,Mangawa Shrawan Kumar¹,Kumar Arvind¹,Dixit A. K.²,Awasthi Satish Kumar¹

Affiliation:

1. Chemical Biology Laboratory, Department of Chemistry; University of Delhi; India-110007 India

2. Department of Chemistry; VSSD College; Kanpur India

Funder

CSIR, India

IUPAC

DST New Delhi, India

University of Delhi, Delhi, India

USIC, University of Delhi

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201701047/fullpdf

Reference79 articles.

1. Evolution of the chalcone-isomerase fold from fatty-acid binding to stereospecific catalysis

2. Stereoselective synthesis of monomeric flavonoids

3. Synthese des Flavanons

4. Conjugate addition to 3-(ptolylsulphinyl)chromone: a route to 2-substituted chromones and chiral substituted chroman-4-ones

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Research Progress on Asymmetric Synthesis of Flavanones;Chinese Journal of Organic Chemistry;2022

2. Catalytic Asymmetric Syntheses of 2‐Aryl Chromenes;Asian Journal of Organic Chemistry;2019-08-12

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