Reaction of Aldonitrones with N-Phenyl-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboximide

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Reaction of Aldonitrones with N-Phenyl-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboximide. / Молчанов, Александр Павлович ; Ефремова, Мария Михайловна ; Степаков, Александр Владимирович ; Паникоровский, Тарас Леонидович ; Костиков, Рафаэль Равилович.

в: Russian Journal of Organic Chemistry, Том 54, № 3, 03.2018, стр. 463-468.

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

BibTeX

@article{78cfc22d6ac44078ab4b59f0e915dab7,

title = "Reaction of Aldonitrones with N-Phenyl-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboximide",

abstract = "Thermal addition of aldonitrones (C,N-diaryl- and N-aryl-C-arylcarbamoylnitrones) to the double bond of N-phenyl-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboximide yields heteropropellanes containing isoxazolidine and pyrrolidine fragments. The cycloaddition of C,N-diarylnitrones is stereoselective, and only one diastereoisomer is formed.",

keywords = "INFLUENZA-A VIRUS, INHIBITORS, M2 ION-CHANNEL, PROPELLANES, TAXANE, TAXUS-CANADENSIS NEEDLES, V27A MUTANT, WILD-TYPE",

author = "Молчанов, {Александр Павлович} and Ефремова, {Мария Михайловна} and Степаков, {Александр Владимирович} and Паникоровский, {Тарас Леонидович} and Костиков, {Рафаэль Равилович}",

note = "Funding Information: This study was performed under financial support by the Russian Foundation for Basic Research (project no. 15-03-05 319) using the facilities of the Center for X-ray Diffraction Studies, Magnetic Resonance Research Center, Chemical Analysis and Materials Research Center, and Chemistry Educational Center of the St. Petersburg State University.",

year = "2018",

month = mar,

doi = "10.1134/S1070428018030144",

language = "English",

volume = "54",

pages = "463--468",

journal = "Russian Journal of Organic Chemistry",

issn = "1070-4280",

publisher = "МАИК {"}Наука/Интерпериодика{"}",

number = "3",

}

RIS

TY - JOUR

T1 - Reaction of Aldonitrones with N-Phenyl-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboximide

AU - Молчанов, Александр Павлович

AU - Ефремова, Мария Михайловна

AU - Степаков, Александр Владимирович

AU - Паникоровский, Тарас Леонидович

AU - Костиков, Рафаэль Равилович

N1 - Funding Information: This study was performed under financial support by the Russian Foundation for Basic Research (project no. 15-03-05 319) using the facilities of the Center for X-ray Diffraction Studies, Magnetic Resonance Research Center, Chemical Analysis and Materials Research Center, and Chemistry Educational Center of the St. Petersburg State University.

PY - 2018/3

Y1 - 2018/3

N2 - Thermal addition of aldonitrones (C,N-diaryl- and N-aryl-C-arylcarbamoylnitrones) to the double bond of N-phenyl-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboximide yields heteropropellanes containing isoxazolidine and pyrrolidine fragments. The cycloaddition of C,N-diarylnitrones is stereoselective, and only one diastereoisomer is formed.

AB - Thermal addition of aldonitrones (C,N-diaryl- and N-aryl-C-arylcarbamoylnitrones) to the double bond of N-phenyl-9,10-dihydro-9,10-ethenoanthracene-11,12-dicarboximide yields heteropropellanes containing isoxazolidine and pyrrolidine fragments. The cycloaddition of C,N-diarylnitrones is stereoselective, and only one diastereoisomer is formed.

KW - INFLUENZA-A VIRUS

KW - INHIBITORS

KW - M2 ION-CHANNEL

KW - PROPELLANES

KW - TAXANE

KW - TAXUS-CANADENSIS NEEDLES

KW - V27A MUTANT

KW - WILD-TYPE

UR - http://www.scopus.com/inward/record.url?scp=85048207248&partnerID=8YFLogxK

UR - http://www.mendeley.com/research/reaction-aldonitrones-nphenyl910dihydro910ethenoanthracene1112dicarboximide

U2 - 10.1134/S1070428018030144

DO - 10.1134/S1070428018030144

M3 - Article

VL - 54

SP - 463

EP - 468

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 3

ER -

ID: 34615821