1,1′-Carbonyldiimidazole as a cyclodehydrating agent for the Castagnoli–Cushman reaction of dicarboxylic acids and imines

Результат исследований: Научные публикации в периодических изданияхстатья

Выдержка

A novel protocol for the Castagnoli–Cushman reaction of dicarboxylic acids and imines comprises the use of 1,1′-carbonyldiimidazole as the cyclodehydrating agent to in situ produce the intermediate anhydrides. In contrast to previously developed procedure involving the use of acetic anhydride, the current protocol allows one to utilize substrates prone to acylation or acid-promoted transformations, which significantly broadens the reaction scope of lactams to be obtained.

Язык оригиналаанглийский
Страницы (с-по)292-293
ЖурналMendeleev Communications
Том29
Номер выпуска3
DOI
СостояниеОпубликовано - 1 мая 2019

Отпечаток

Lactams
Acylation
Dicarboxylic Acids
Imines
Anhydrides
Acids
Substrates
acetic anhydride

Предметные области Scopus

  • Химия (все)

Цитировать

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abstract = "A novel protocol for the Castagnoli–Cushman reaction of dicarboxylic acids and imines comprises the use of 1,1′-carbonyldiimidazole as the cyclodehydrating agent to in situ produce the intermediate anhydrides. In contrast to previously developed procedure involving the use of acetic anhydride, the current protocol allows one to utilize substrates prone to acylation or acid-promoted transformations, which significantly broadens the reaction scope of lactams to be obtained.",
author = "Chupakhin, {Evgeny G.} and Bakulina, {Olga Yu} and Dar'in, {Dmitry V.} and Mikhail Krasavin",
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1,1′-Carbonyldiimidazole as a cyclodehydrating agent for the Castagnoli–Cushman reaction of dicarboxylic acids and imines. / Chupakhin, Evgeny G.; Bakulina, Olga Yu; Dar'in, Dmitry V.; Krasavin, Mikhail.

В: Mendeleev Communications , Том 29, № 3, 01.05.2019, стр. 292-293.

Результат исследований: Научные публикации в периодических изданияхстатья

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AU - Krasavin, Mikhail

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