[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles

Ilya V. Efimov; Maria D. Matveeva; Rafael Luque; Vasiliy A. Bakulev; Leonid G. Voskressensky

doi:10.1002/ejoc.201901776

[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles

Ilya V. Efimov, Maria D. Matveeva, Rafael Luque, Vasiliy A. Bakulev, Leonid G. Voskressensky

Результат исследований: Вклад в журнал › Статья

Язык оригинала	Английский
Страницы (с-по)	1108-1113
Число страниц	6
Журнал	European Journal of Organic Chemistry
Том	2020
Номер выпуска	9
DOI	https://doi.org/10.1002/ejoc.201901776
Состояние	Опубликовано - 8 мар 2020

Предметные области ASJC Scopus

Physical and Theoretical Chemistry
Organic Chemistry

Предметные области WoS

Химия, Органическая

Ссылки

10.1002/ejoc.201901776

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Упоминания в прессе

Chemists propose a new method for the synthesis of pyrroles

I. V. Efimov & V. A. Bakulev

05/10/2020

1 Материалы средств информации

Пресса/СМИ: другое

Цитировать

Efimov, I. V., Matveeva, M. D., Luque, R., Bakulev, V. A., & Voskressensky, L. G. (2020). [3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles. European Journal of Organic Chemistry, 2020(9), 1108-1113. https://doi.org/10.1002/ejoc.201901776

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title = "[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles",

keywords = "Cycloaddition, Enamines, Enaminones, Isocyanides, Potassium tert-butoxide, Pyrroles, AZIDES, OLIGOSUBSTITUTED PYRROLES, SUBSTITUTED PYRROLES, CLICK CHEMISTRY, CATALYZED REACTION, ALKYNES, PYRROLE-2-CARBOXYLATES, REGIOSELECTIVE SYNTHESIS, DERIVATIVES, CHLORIN",

author = "Efimov, {Ilya V.} and Matveeva, {Maria D.} and Rafael Luque and Bakulev, {Vasiliy A.} and Voskressensky, {Leonid G.}",

year = "2020",

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doi = "10.1002/ejoc.201901776",

language = "English",

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journal = "European Journal of Organic Chemistry",

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}

[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles. / Efimov, Ilya V.; Matveeva, Maria D.; Luque, Rafael; Bakulev, Vasiliy A.; Voskressensky, Leonid G.

В: European Journal of Organic Chemistry, Том 2020, № 9, 08.03.2020, стр. 1108-1113.

Результат исследований: Вклад в журнал › Статья

TY - JOUR

T1 - [3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles

AU - Efimov, Ilya V.

AU - Matveeva, Maria D.

AU - Luque, Rafael

AU - Bakulev, Vasiliy A.

AU - Voskressensky, Leonid G.

PY - 2020/3/8

Y1 - 2020/3/8

KW - Cycloaddition

KW - Enamines

KW - Enaminones

KW - Isocyanides

KW - Potassium tert-butoxide

KW - Pyrroles

KW - AZIDES

KW - OLIGOSUBSTITUTED PYRROLES

KW - SUBSTITUTED PYRROLES

KW - CLICK CHEMISTRY

KW - CATALYZED REACTION

KW - ALKYNES

KW - PYRROLE-2-CARBOXYLATES

KW - REGIOSELECTIVE SYNTHESIS

KW - DERIVATIVES

KW - CHLORIN

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DO - 10.1002/ejoc.201901776

M3 - Article

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SP - 1108

EP - 1113

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

SN - 1434-193X

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ER -