Sulfenylation of Indoles Mediated by Iodine and Its Compounds

Sulfenylation of Indoles Mediated by Iodine and Its Compounds Review

Journal

ChemistrySelect
ISSN: 2365-6549

Output data

Year: 2021, Volume: 6, Number: 38, Pages: 10369-10378 Pages count : 10 DOI: 10.1002/slct.202102227

Authors

Mulina Olga M. ¹ , Ilovaisky Alexey I. ^1,2 , Terent'ev Alexander O. ¹

Affiliations

1	Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prospect, 119991 Moscow, Russian Federation
2	All Russian Research Institute for Phytopathology, B. Vyazyomy, 143050 Moscow Region, Russian Federation

Indole represents one of the most common and important heterocyclic scaffolds omnipresent in a plenty of natural products and medicinal agents. Development of the synthetic routes to 3-substituted indoles attracts a considerable attention due to a huge amount of biologically relevant molecules containing 3-substituted indole moiety. Reactions of indoles halogenation, nitration, acylation, and alkylation at the 3d position have been known for several decades and continue developing now. Processes of indoles sulfenylation are much less studied. However, 3-sulfenylated derivatives possess promising biological properties. This review summarizes nearly 100 references from the middle of the 20th century to 2021, concerning reactions of indoles sulfenylation mediated by iodine and its compounds. The manuscript is divided into the sections according to the classes of compounds used as sulfenylating agents.

Mulina O.M. , Ilovaisky A.I. , Terent'ev A.O.
Sulfenylation of Indoles Mediated by Iodine and Its Compounds
ChemistrySelect. 2021. V.6. N38. P.10369-10378. DOI: 10.1002/slct.202102227 WOS Scopus OpenAlex

Web of science:	WOS:000706994200030
Scopus:	2-s2.0-85117131585
OpenAlex:	W3205073967

DB	Citing
OpenAlex	3
Scopus	5