N-propargyl aza-Claisen rearrangement in the synthesis of heterocycles

Pericyclic reactions present a convenient tool for constructing heterocyclic systems. They make possible to obtain quite complex structures in one step with high yields and stereoselectivity. A special position in this series is assigned to the named reactions of [3,3]-sigmatropic transformations, including the aza-Claisen one. This rearrangement lately found its brilliant continuation in N-propargyl variant. In the present short review we have tried to provide an overview of the practical application of N-propargyl aza-Claisen rearrangement in the construction of pyrrole, pyridine and medium aza-heterocycle derivatives focusing mainly on literature data on the XXI century. © 2022 Elsevier Ltd

Авторы
Listratova A.V. , Titov A.A. , Obydennik A.Y. , Varlamov A.V.
Журнал
Язык
Английский
Статус
Опубликовано
Номер
132914
Том
121
Год
2022
Организации
  • 1 Organic Chemistry Department, Рeoples’ Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
Ключевые слова
Medium azacyclic allenes; N-propargyl aza-Claisen rearrangement, Pyrroles; Pericyclic reaction; Pyridines
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