Tandem transformations of tetrahydropyrrolo[3,2-c]pyridines under the action of dimethyl acetylenedicarboxylate. A novel route to pyrrolo[2,3-d] azocines

Reactions of substituted tetrahydropyrrolo[3,2-c]pyridines with dimethyl acetylene-dicarboxylate in protic and aprotic solvents were studied. A novel single-step method for the synthesis of pyrrolo[2,3-d]azocine derivatives was developed. © 2005 Springer Science+Business Media, Inc.

Номер выпуска
11
Язык
Английский
Страницы
2594-2601
Статус
Опубликовано
Том
54
Год
2005
Организации
  • 1 Peoples Friendship University, 6 ul. Miklukho-Maklaya, 117198 Moscow, Russian Federation
Ключевые слова
Pyrrolo[2,3-d]azocines; Tandem opening; Tetrahydropyrrolo[3,2-c]pyridines
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