Synthesis of sulfolanooctahydrochromenones from 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides

Standard

Synthesis of sulfolanooctahydrochromenones from 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides. / Savelev, Igor I.; Efremova, Irina E.; Lapshina, Lidiya V.; Gurzhiy, Vladislav V.; Baichurin, Ruslan I.

в: Chemistry of Heterocyclic Compounds, Том 58, № 1, 01.2022, стр. 58-63.

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

Author

Savelev, Igor I. ; Efremova, Irina E. ; Lapshina, Lidiya V. ; Gurzhiy, Vladislav V. ; Baichurin, Ruslan I. / Synthesis of sulfolanooctahydrochromenones from 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides. в: Chemistry of Heterocyclic Compounds. 2022 ; Том 58, № 1. стр. 58-63.

BibTeX

@article{747a90e90db94abe990cac075eee8819,

title = "Synthesis of sulfolanooctahydrochromenones from 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides",

abstract = "[Figure not available: see fulltext.] The reactions of 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides with dimedone were used to synthesize a series of tricyclic compounds containing fused nitrosulfolane and octahydrochromenone rings. The structural features of the obtained polycyclic compounds were established on the basis of IR and NMR spectra, as well as X-ray structural analysis.",

keywords = "2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides, enolizable cyclic СН acids, sulfolenes, tandem process",

author = "Savelev, {Igor I.} and Efremova, {Irina E.} and Lapshina, {Lidiya V.} and Gurzhiy, {Vladislav V.} and Baichurin, {Ruslan I.}",

note = "Publisher Copyright: {\textcopyright} 2022, Springer Science+Business Media, LLC, part of Springer Nature.",

year = "2022",

month = jan,

doi = "10.1007/s10593-022-03056-z",

language = "English",

volume = "58",

pages = "58--63",

journal = "Chemistry of Heterocyclic Compounds",

issn = "0009-3122",

publisher = "Springer Nature",

number = "1",

}

RIS

TY - JOUR

T1 - Synthesis of sulfolanooctahydrochromenones from 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides

AU - Savelev, Igor I.

AU - Efremova, Irina E.

AU - Lapshina, Lidiya V.

AU - Gurzhiy, Vladislav V.

AU - Baichurin, Ruslan I.

PY - 2022/1

Y1 - 2022/1

N2 - [Figure not available: see fulltext.] The reactions of 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides with dimedone were used to synthesize a series of tricyclic compounds containing fused nitrosulfolane and octahydrochromenone rings. The structural features of the obtained polycyclic compounds were established on the basis of IR and NMR spectra, as well as X-ray structural analysis.

AB - [Figure not available: see fulltext.] The reactions of 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides with dimedone were used to synthesize a series of tricyclic compounds containing fused nitrosulfolane and octahydrochromenone rings. The structural features of the obtained polycyclic compounds were established on the basis of IR and NMR spectra, as well as X-ray structural analysis.

KW - 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides

KW - enolizable cyclic СН acids

KW - sulfolenes

KW - tandem process

UR - http://www.scopus.com/inward/record.url?scp=85123991048&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/5c08c735-3acc-3ab6-abae-bf454d22d475/

U2 - 10.1007/s10593-022-03056-z

DO - 10.1007/s10593-022-03056-z

M3 - Article

AN - SCOPUS:85123991048

VL - 58

SP - 58

EP - 63

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 1

ER -

ID: 98952836