Asymmetric Synthesis of Cyclohexenone-Fused Isochromans via Quinidine-Catalyzed Domino Peroxyhemiacetalization/Oxa-Michael Addition/Desymmetrization Sequence-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Cyclohexenone-Fused Isochromans via Quinidine-Catalyzed Domino Peroxyhemiacetalization/Oxa-Michael Addition/Desymmetrization Sequence

Published:2022-04-19 Issue:9 Volume:87 Page:6397-6402
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Tamanna ¹,Hussain Yaseen¹,Sharma Deepak¹,Chauhan Pankaj¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Jammu, Jagti, NH-44, Nagrota Bypass, Jammu 181221, J&K, India

Funder

University Grants Commission

Science and Engineering Research Board

Indian Institute of Technology Jammu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00215

Reference45 articles.

1. An Alkaloid with a Novel Skeleton from the Roots ofStephania excentrica

2. (S)-(−)-4-[4-[2-(Isochroman-1-yl)ethyl]piperazin-1-yl]benzenesulfonamide, a Selective Dopamine D4 Antagonist

3. 2-N-Methylexcentricine, a New Alkaloid from Roots of Stephania excentrica

4. Isochroman-6-carboxamides as Highly Selective 5-HT1D Agonists: Potential New Treatment for Migraine without Cardiovascular Side Effects

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