A Concise Approach for the Synthesis of the ABCD Ring System of Alpkinidine

A two step synthesis of a benzo analog of alpkinidine is described via Negishi coupling followed by a base mediated annulation reaction strategy. The organozinc compound prepared from ethyl 2-iodobenzoate was coupled with 4-chloro-2-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]quinolin-1-one to obtain ethyl 2-(2-methyl-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]quinolin-4-yl)-benzoate which on further treatment with a base provided ABCD ring system of alpkinidine. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Authors
Volvoikar P.S.1 , Tilve S.G. 1 , Zubkov F.I. 2
Journal
Publisher
Wiley-Blackwell
Number of issue
24
Language
English
Pages
7187-7189
Status
Published
Volume
4
Year
2019
Organizations
  • 1 School of Chemical Sciences, Goa University, Taleigao Plateau, Goa 403206, India
  • 2 Organic Chemistry Department, RUDN University, 6 Miklukcho-Maklaya str., Moscow, 117198, Russian Federation
Keywords
Alpkinidine; Heterocycles; Marine alkaloid; Marine alkaloid; Negishi; Pyrroloacridine
Date of creation
19.07.2019
Date of change
19.07.2019
Short link
https://repository.rudn.ru/en/records/article/record/38575/
Share

Other records