Bioinspired cyclization of in situ generated γ-indolyl β,γ-unsaturated α-keto esters via an oxidative enamine process: facile approaches to pyrano[2,3-b]indoles
Author:
Affiliation:
1. Key Laboratory of Optic-electric Sensing and Analytic Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science & Technology, Qingdao 266042, China
Abstract
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00996F
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1. Hyrtimomines A–C, New Heteroaromatic Alkaloids from a Sponge Hyrtios sp.
2. Goniomedines A and B: Unprecedented Bisindole Alkaloids Formed through Fusion of Two Indole Moieties via a Dihydropyran Unit
3. Bipleiophylline, an Unprecedented Cytotoxic Bisindole Alkaloid Constituted from the Bridging of Two Indole Moieties by an Aromatic Spacer Unit
4. Tryptophan derived natural marine alkaloids and synthetic derivatives as promising antimicrobial agents
5. Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted chromeno[2,3-b]indoles
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3. Efficient radical C(sp3)–H α-oxyamination of carbonyls adjacent to the carbon chalcogen bond;Organic Chemistry Frontiers;2022
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