A One-Pot Direct Iodination of the Fischer–Borsche Ring Using Molecular Iodine and Its Utility in the Synthesis of 6‑Oxygenated Carbazole Alkaloids

An efficient regioselective iodination of the Fischer–Borsche ring has been achieved using molecular iodine, in a one-pot synthesis. The acid-, metal-, and oxidant-free conditions of the present method are highly convenient and practical. Furthermore, the one-pot direct iodination process is extende...

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Bibliographic Details
Published in:Journal of organic chemistry 2015-02, Vol.80 (4), p.2392-2396
Main Authors: Naykode, Mahavir S, Humne, Vivek T, Lokhande, Pradeep D
Format: Article
Language:English
Subjects:
alkaloids
Alkaloids - chemical synthesis
Alkaloids - chemistry
Carbazoles - chemical synthesis
Carbazoles - chemistry
iodination
iodine
Iodine - chemistry
moieties
Molecular Structure
organic chemistry
Oxygen - chemistry
regioselectivity
Stereoisomerism
synthesis
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