Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine

Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine Full article

Journal

Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388

Output data

Year: 2021, Volume: 57, Number: 6, Pages: 1062–1065 Pages count : DOI: 10.1007/s10600-021-03550-4

Tags

alkanesulfonyl chloride; berberine; cycloaddition; dihydroberberine; sulfone

Authors

Gladkova E.D. ^1,2 , Luzina O.A. ¹ , Salakhutdinov N.F. ¹

Affiliations

1	N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, 9 Prosp. Lavrent’eva, Novosibirsk, 630090, Russian Federation
2	Novosibirsk State University, Pirogova St, Novosibirsk, 630090, Russian Federation

Novel berberine derivatives with annelated four-membered sulfone rings were synthesized. Cycloaddition of alkanesulfonyl chlorides to dihydroberberine occurred with high stereoselectivity and formed a single stereoisomer. © 2021, Springer Science+Business Media, LLC, part of Springer Nature.

Gladkova E.D. , Luzina O.A. , Salakhutdinov N.F.
Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine
Chemistry of Natural Compounds. 2021. V.57. N6. P.1062–1065. DOI: 10.1007/s10600-021-03550-4 WOS Scopus

Web of science	WOS:000719736400008
Scopus	2-s2.0-85119184941
OpenAlex	W4200355586