88368-15-4Relevant academic research and scientific papers
Syntheses of N-alkylated carbazolones via Pd(OAc)2-mediated intramolecular coupling of N-substituted 3-(arylamino)cyclohex-2-enones
Bi, Wenying,Yun, Xiliu,Fan, Yanfeng,Qi, Xiuxiang,Du, Yunfei,Huang, Jianhui
supporting information; experimental part, p. 2899 - 2904 (2011/02/25)
A variety of functionalized N-alkylated carbazolones were prepared via N-alkylation of 3-(arylamino)cyclohex-2-enones followed by an intramolecular oxidative coupling mediated by Pd(OAc)2 under an oxygen atmosphere. This approach adopts an inverted sequence, consisting of the conventional annulation and subsequent N-alkylation. Georg Thieme Verlag Stuttgart - New York.
Synthese de Dihydro-6,7 5H-pyrimidinocarbazoles et de 7H-Pyrimidinocarbazoles
Lancelot, Jean-Charles,Gazengel, Jean-Marie,Robba, Max
, p. 2652 - 2661 (2007/10/02)
The synthesis of 6,7-dihydro-5H-pyrimidinocarbazoles (3) was achived by cyclisation of 1,2,3,4-tetrahydrocarbazol-4-ones with triformamidomethane.The oxydation with potassium permanganate of 6,7-dihydro-5H-pyrimidinocarbazoles gave the 7H-pyrimidinocarbazoles (4).The reactions of the pyrimidinocarbazoles (4a) and (4e) with lithium organic compounds afforded 4-substituted derivatives (6).The structure of the derivatives was determined by (1)H-NMR and Overhauser effect.Keywords - 1,2,3,4-tetrahydrocarbazol-4-one; 6,7-dihydro-5H-pyrimidinocarbazole; 7H-pyrimidinocarbazole; (1)H-NMR; Overhauser effect
