Rhodium-catalyzed C–H activation/annulation of amidines with 4-diazoisochroman-3-imines toward isochromeno[3,4-c]isoquinolines
Author:
Affiliation:
1. School of Petrochemical Engineering
2. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology
3. and Jiangsu Province Key Laboratory of Fine Petrochemical Engineering
4. Changzhou University
5. Changzhou
Abstract
Rhodium-catalyzed C–H activation/annulation of amidines with 4-diazoisochroman-3-imines toward 8-amino-5H-isochromeno[3,4-c]isoquinolines with good functional group tolerance.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Jiangsu Province
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology Department
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB01612K
Reference58 articles.
1. Anticancer and Reversing Multidrug Resistance Activities of Natural Isoquinoline Alkaloids and their Structure-activity Relationship
2. Selective inhibition of monoamine oxidase A by chelerythrine, an isoquinoline alkaloid
3. Six-Membered Ring Systems
4. Effective Synthetic Strategies for the Construction of Isoquinoline Scaffold Found in Biologically Active Natural Products
5. Isoquinoline Alkaloids and Their Antiviral, Antibacterial, and Antifungal Activities and Structure-activity Relationship
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