Photoredox-Catalyzed Isatin Reactions: Access to Dibenzo-1,7-Naphthyridine Carboxylate and Tryptanthrin
Author:
Affiliation:
1. Natural Product Microbes and ACSIR; CSIR-Indian Institute of Integrative Medicine; Jammu 180001 India
2. Department of Physics; University of Jammu; Jammu 180001 India
Funder
Department of Sceince and Technology
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Analytical Chemistry
Reference99 articles.
1. Photoinduced [2 + 2] cycloadditions (the Paterno–Büchi reaction) of 1H-1-acetylindole-2,3-dione with alkenes
2. Photoinduced [2+2] cycloadditions (the Paterno–Büchi reaction) of 1-acetylisatin with enol ethers—regioselectivity, diastereoselectivity and acid catalysed transformations of the spirooxetane productsElectronic supplementary information (ESI) available: NMR spectra and ORTEP diagrams. Crystallographic data for compounds 10, 17 and 23 are included in the ESI. CCDC numbers 175732, 175733 and 175736. See http://www.rsc.org/suppdata/p1/b1/b109697d/
3. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks
4. Recent Advances in Diversity Oriented Synthesis through Isatin-based Multicomponent Reactions
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