Practical synthesis of amides from in situ generated copper(I) acetylides and sulfonyl azides

Michael P. Cassidy, Jessica Raushel, Valery V. Fokin

Результат исследований: Материалы для журналаСтатья

220 Цитирования (Scopus)

Выдержка

(Chemical Equation Presented) A direct, simple, and efficient route from terminal alkynes to amides is achieved by their copper(I)-catalyzed reaction with sulfonyl azides (see scheme). The reaction proceeds with the in situ generation of copper(I) acetylides and represents a one-step formal oxidative hydration of a triple bond.

Язык оригиналаАнглийский
Страницы (с-по)3154-3157
Число страниц4
ЖурналAngewandte Chemie - International Edition
Том45
Номер выпуска19
DOI
СостояниеОпубликовано - 5 мая 2006
Опубликовано для внешнего пользованияДа

Отпечаток

Azides
Amides
Copper
Alkynes
Hydration

ASJC Scopus subject areas

  • Chemistry(all)

Цитировать

Practical synthesis of amides from in situ generated copper(I) acetylides and sulfonyl azides. / Cassidy, Michael P.; Raushel, Jessica; Fokin, Valery V.

В: Angewandte Chemie - International Edition, Том 45, № 19, 05.05.2006, стр. 3154-3157.

Результат исследований: Материалы для журналаСтатья

Cassidy, Michael P. ; Raushel, Jessica ; Fokin, Valery V. / Practical synthesis of amides from in situ generated copper(I) acetylides and sulfonyl azides. В: Angewandte Chemie - International Edition. 2006 ; Том 45, № 19. стр. 3154-3157.
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