Organocatalytic, Enantioselective, Intramolecular Oxa-Michael Reaction of Alkoxyboronate: A New Strategy for Enantioenriched 1-Substituted 1,3-Dihydroisobenzofurans-Reference-Cited by-同舟云学术

Organocatalytic, Enantioselective, Intramolecular Oxa-Michael Reaction of Alkoxyboronate: A New Strategy for Enantioenriched 1-Substituted 1,3-Dihydroisobenzofurans

Published:2014-10-22 Issue:21 Volume:16 Page:5580-5583
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ravindra Barnala¹,Das Braja Gopal¹,Ghorai Prasanta¹

Affiliation:

1. Department of Chemistry, Indian Institute of Science Education and Research Bhopal, Bhauri, Bhopal 462066, India

Funder

Council of Scientific and Industrial Research

Indian Institute of Science Education and Research Bhopal

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol502614n

Reference62 articles.

1. Pestacin: a 1,3-dihydro isobenzofuran from Pestalotiopsis microspora possessing antioxidant and antimycotic activities

2. A synthetic route to 1,3-dihydroisobenzofuran natural products: the synthesis of methyl ethers of pestacin

3. The selective serotonin reuptake inhibitor citalopram relieves the symptoms of diabetic neuropathy

4. Citalopram Therapy for Depression

5. Improved One-Pot Synthesis of Citalopram Diol and Its Conversion to Citalopram

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