Alkylation of 2, 3-Dimethylindole in Liquid Ammonia
M Nakazaki
Index: Nakazaki Bulletin of the Chemical Society of Japan, 1959 , vol. 32, p. 838
Full Text: HTML
Citation Number: 13
Abstract
In the previous paper0, formation of both 9-alkyltetrahydrocarbazoles (IIa, b, c) and 11- alkyltetrahydrocarbazolenines (Ilia, b, c) by the alkylation of tetrahydrocarbazole (I) in liquid ammonia with sodium amide and alkyl halides was reported. But, when isopropyl iodide was employed as alkylation reagent, 11-isopropyltetrahydrocarbazolenine (Hid) was a sole product isolated. These 11-alkyltetrahydrocarbazolenines could be also prepared by the ...
Related Articles:
Palladium-Catalyzed Decarboxylative Allylation and Benzylation of N-Alloc and N-Cbz Indoles
[Montgomery, Thomas D.; Zhu, Ye; Kagawa, Natsuko; Rawal, Viresh H. Organic Letters, 2013 , vol. 15, # 5 p. 1140 - 1143]
N-Indolyltriethylborate: A Useful Reagent for Synthesis of C3-Quaternary Indolenines
[Lin, Aijun; Yang, Jiong; Hashim, Mohamed Organic Letters, 2013 , vol. 15, # 8 p. 1950 - 1953]
[Zimmermann, Thomas; Hennig, Lothar Journal of Heterocyclic Chemistry, 2002 , vol. 39, # 2 p. 263 - 269]