3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines

Igor B. Kutyashev; Alexey Yu Barkov; Vladislav Yu Korotaev; Vyacheslav Ya Sosnovskikh

doi:10.1007/s10593-019-02490-w

3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines

Igor B. Kutyashev, Alexey Yu Barkov, Vladislav Yu Korotaev, Vyacheslav Ya Sosnovskikh

Результат исследований: Вклад в журнал › Статья › рецензирование

Язык оригинала	Английский
Страницы (с-по)	529-540
Число страниц	12
Журнал	Chemistry of Heterocyclic Compounds
Том	55
Номер выпуска	6
DOI	https://doi.org/10.1007/s10593-019-02490-w
Состояние	Опубликовано - 15 июн 2019

Предметные области ASJC Scopus

Organic Chemistry

Предметные области WoS

Химия, Органическая

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10.1007/s10593-019-02490-w

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Научная лаборатория «Контролируемого синтеза сложных молекулярных систем»
Сосновских, В. Я., Барков, А. Ю., Коротаев, В. Ю., Мошкин, В. С., Обыденнов, Д. Л., Кутяшев, И. Б. & Усачев, С. А.
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Kutyashev, I. B., Barkov, A. Y., Korotaev, V. Y., & Sosnovskikh, V. Y. (2019). 3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines. Chemistry of Heterocyclic Compounds, 55(6), 529-540. https://doi.org/10.1007/s10593-019-02490-w

Kutyashev, Igor B. ; Barkov, Alexey Yu ; Korotaev, Vladislav Yu ; Sosnovskikh, Vyacheslav Ya. / 3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines. В: Chemistry of Heterocyclic Compounds. 2019 ; Том 55, № 6. стр. 529-540.

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title = "3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines",

keywords = "1,3-dipolar cycloaddition, 3-nitro-2H-chromenes, isatins, N-unsubstituted α-amino acids, spirochromeno[3,4-c]pyrrolidines, stabilized azomethine ylides, NATURAL-PRODUCTS, 3-dipolar cycloaddition, DISCOVERY, SPIROOXINDOLES, spirochromeno[3, 1, N-unsubstituted alpha-amino acids, FACILE SYNTHESIS, HETEROCYCLES, 4-c]pyrrolidines, 1,3-DIPOLAR CYCLOADDITION, CONSTRUCTION, 3,3,3-TRIHALOGENO-1-NITROPROPENES SYNTHESIS, MICROWAVE-ASSISTED SYNTHESIS, DERIVATIVES",

author = "Kutyashev, {Igor B.} and Barkov, {Alexey Yu} and Korotaev, {Vladislav Yu} and Sosnovskikh, {Vyacheslav Ya}",

year = "2019",

month = jun,

day = "15",

doi = "10.1007/s10593-019-02490-w",

language = "English",

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journal = "Chemistry of Heterocyclic Compounds",

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Kutyashev, IB , Barkov, AY , Korotaev, VY & Sosnovskikh, VY 2019, '3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines', Chemistry of Heterocyclic Compounds, том. 55, № 6, стр. 529-540. https://doi.org/10.1007/s10593-019-02490-w

3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines. / Kutyashev, Igor B.; Barkov, Alexey Yu ; Korotaev, Vladislav Yu ; Sosnovskikh, Vyacheslav Ya.

В: Chemistry of Heterocyclic Compounds, Том 55, № 6, 15.06.2019, стр. 529-540.

Результат исследований: Вклад в журнал › Статья › рецензирование

TY - JOUR

T1 - 3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines

AU - Kutyashev, Igor B.

AU - Barkov, Alexey Yu

AU - Korotaev, Vladislav Yu

AU - Sosnovskikh, Vyacheslav Ya

PY - 2019/6/15

Y1 - 2019/6/15

KW - 1,3-dipolar cycloaddition

KW - 3-nitro-2H-chromenes

KW - isatins

KW - N-unsubstituted α-amino acids

KW - spirochromeno[3,4-c]pyrrolidines

KW - stabilized azomethine ylides

KW - NATURAL-PRODUCTS

KW - 3-dipolar cycloaddition

KW - DISCOVERY

KW - SPIROOXINDOLES

KW - spirochromeno[3

KW - 1

KW - N-unsubstituted alpha-amino acids

KW - FACILE SYNTHESIS

KW - HETEROCYCLES

KW - 4-c]pyrrolidines

KW - 1,3-DIPOLAR CYCLOADDITION

KW - CONSTRUCTION

KW - 3,3,3-TRIHALOGENO-1-NITROPROPENES SYNTHESIS

KW - MICROWAVE-ASSISTED SYNTHESIS

KW - DERIVATIVES

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DO - 10.1007/s10593-019-02490-w

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JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 6

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Kutyashev IB , Barkov AY , Korotaev VY , Sosnovskikh VY. 3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines. Chemistry of Heterocyclic Compounds. 2019 Июнь 15;55(6):529-540. https://doi.org/10.1007/s10593-019-02490-w

3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines

Предметные области ASJC Scopus

Предметные области WoS

Ссылки

Другие файлы и ссылки

Fingerprint

Проекты

Научная лаборатория «Контролируемого синтеза сложных молекулярных систем»

Цитировать