Total assignment of the proton and carbon NMR spectra of the alkaloid quindoline - utilization of HMQC-TOCSY to indirectly establish protonated carbon-protonated carbon connectivities
Author:
Publisher
Wiley
Subject
Organic Chemistry
Reference8 articles.
1. 1H-NMR and13C-NMR Assignments of Cryptolepine, A 3:4-Benz-δ-carboline Derivative Isolated fromCryptolepis sanguinolenta
2. Assignment of the proton and carbon NMR spectra of the indoloquinoline alkaloid cryptolepine
3. Constituents of West African Medicinal Plants XX: Quindoline from Cryptolepis sanguinolenta
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1. Efficient Buchwald–Hartwig and nitrene-mediated five-membered ring closure approaches to the total synthesis of quindoline. Unexpected direct conversion of a nitro group into a phosphazene;RSC Advances;2023
2. A concise Friedländer/Buchwald–Hartwig approach to the total synthesis of quindoline, a bioactive natural indoloquinoline alkaloid, and toward the unnatural 10-methylquindoline;New Journal of Chemistry;2019
3. Isolation, Synthesis, and Biological Activity of Quindoline, a Valuable Indoloquinoline Natural Product and Useful Key Intermediate;Synthesis;2018-02-26
4. Microwave-assisted Iodine-catalyzed Rapid Synthesis of 6H-indolo[2,3-b] quinolines: Formal Synthesis of Cryptotackieine;Current Microwave Chemistry;2017-09-07
5. LC–DAD–MS-based metabolite profiling of three species of Justicia (Acanthaceae);Natural Product Research;2012-11-06
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