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Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine. / Gladkova, E. D.; Luzina, O. A.; Salakhutdinov, N. F.

в: Chemistry of Natural Compounds, Том 57, № 6, 18.11.2021, стр. 1062-1065.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Gladkova, ED, Luzina, OA & Salakhutdinov, NF 2021, 'Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine', Chemistry of Natural Compounds, Том. 57, № 6, стр. 1062-1065. https://doi.org/10.1007/s10600-021-03550-4

APA

Gladkova, E. D., Luzina, O. A., & Salakhutdinov, N. F. (2021). Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine. Chemistry of Natural Compounds, 57(6), 1062-1065. https://doi.org/10.1007/s10600-021-03550-4

Vancouver

Gladkova ED, Luzina OA, Salakhutdinov NF. Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine. Chemistry of Natural Compounds. 2021 нояб. 18;57(6):1062-1065. doi: 10.1007/s10600-021-03550-4

Author

Gladkova, E. D. ; Luzina, O. A. ; Salakhutdinov, N. F. / Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine. в: Chemistry of Natural Compounds. 2021 ; Том 57, № 6. стр. 1062-1065.

BibTeX

@article{b90d231d8da5427b9184fe2ce41d3aa9,
title = "Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine",
abstract = "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.",
keywords = "alkanesulfonyl chloride, berberine, cycloaddition, dihydroberberine, sulfone",
author = "Gladkova, {E. D.} and Luzina, {O. A.} and Salakhutdinov, {N. F.}",
note = "Funding Information: We thank Khimiya Center for Common Use, SB, RAS, for making the spectral and analytical measurements. Publisher Copyright: {\textcopyright} 2021, Springer Science+Business Media, LLC, part of Springer Nature.",
year = "2021",
month = nov,
day = "18",
doi = "10.1007/s10600-021-03550-4",
language = "English",
volume = "57",
pages = "1062--1065",
journal = "Chemistry of Natural Compounds",
issn = "0009-3130",
publisher = "Springer New York",
number = "6",

}

RIS

TY - JOUR

T1 - Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine

AU - Gladkova, E. D.

AU - Luzina, O. A.

AU - Salakhutdinov, N. F.

N1 - Funding Information: We thank Khimiya Center for Common Use, SB, RAS, for making the spectral and analytical measurements. Publisher Copyright: © 2021, Springer Science+Business Media, LLC, part of Springer Nature.

PY - 2021/11/18

Y1 - 2021/11/18

N2 - 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.

AB - 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.

KW - alkanesulfonyl chloride

KW - berberine

KW - cycloaddition

KW - dihydroberberine

KW - sulfone

UR - http://www.scopus.com/inward/record.url?scp=85119184941&partnerID=8YFLogxK

U2 - 10.1007/s10600-021-03550-4

DO - 10.1007/s10600-021-03550-4

M3 - Article

AN - SCOPUS:85119184941

VL - 57

SP - 1062

EP - 1065

JO - Chemistry of Natural Compounds

JF - Chemistry of Natural Compounds

SN - 0009-3130

IS - 6

ER -

ID: 34679702