120106-18-5Relevant academic research and scientific papers
Total synthesis of (-)-serotobenine
Koizumi, Yasuaki,Kobayashi, Hideki,Wakimoto, Toshiyuki,Furuta, Takumi,Fukuyama, Tohru,Kan, Toshiyuki
supporting information; experimental part, p. 16854 - 16855 (2009/04/13)
The efficient total synthesis of (?)-serotobenine (1) has been achieved by constructing an optically active dihydrobenzofuran ring via a rhodium carbenoid mediated intramolecular C?H insertion reaction, which was developed by our group. Then the possibili
The synthesis of pyrano[3,2-e]indoles and pyrano[2,3-f]indoles as rotationally restricted phenolic analogs of the neurotransmitter serotonin
Macor,Ryan,Newman
, p. 1039 - 1052 (2007/10/02)
The synthesis of two rotationally restricted phenolic analogs (1a and 1b) of the neurotransmitter serotonin have been accomplished. The syntheses of 8,9-dihydropyrano[3,2-e]indole (13a) and 7,8-dihydropyrano[2,3-f]indole (13b), which formed the template f
CHEMISTRY OF 6H-PYRIDOCARBAZOLES. PART 13. SYNTHESES OF RING-A- AND RING-D-SUBSTITUTED ELLIPTICINES
Sainsbury, Malcolm,Smith, Andrew D.,Vong, Kuok K.,Scopes, David I. C.
, p. 2945 - 2954 (2007/10/02)
The syntheis of 3-hydroxymethyl-5,11-dimethyl-6H-pyridocarbazole is described, and uses a modified Cranwell-Saxton approach to ellipticines.The rearrangement of 9-allyl-6-methoxy-1,4-dimethylcarbazole to the 8-allyl isomer has been employed as the
