Thianaphtheno [3, 2-c] pyridine and Certain Derivatives
DB Capps, CS Hamilton
Index: Capps; Hamilton Journal of the American Chemical Society, 1953 , vol. 75, p. 697
Full Text: HTML
Citation Number: 3
Abstract
2-Thianaphthenyl sodium was treated with ethylene oxide, giving 2-thianaphthene-ethanol. The alcohol was converted to its chloro analog and the latter to the iodo compound, which gave 2-thianaphthene-ethylamine by Gabriel's phthalimide reaction. 2-Thianaphthene- ethylamine was benzoylated and acetylated yielding amides which were converted to the corresponding dihydroisoquinoline-like compounds by the Bischler-Napieralski reaction. ...
Related Articles:
[Kennis, Ludo E.J.; Bischoff, Francois P.; Mertens, Carolus J.; Love, Christopher J.; Van den Keybus, Frans A.F.; Pieters, Serge; Braeken, Mirielle; Megens, Anton A.H.P.; Leysen, Josee E. Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 1 p. 71 - 74]
[Kennis, Ludo E.J.; Bischoff, Francois P.; Mertens, Carolus J.; Love, Christopher J.; Van den Keybus, Frans A.F.; Pieters, Serge; Braeken, Mirielle; Megens, Anton A.H.P.; Leysen, Josee E. Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 1 p. 71 - 74]
[Kennis, Ludo E.J.; Bischoff, Francois P.; Mertens, Carolus J.; Love, Christopher J.; Van den Keybus, Frans A.F.; Pieters, Serge; Braeken, Mirielle; Megens, Anton A.H.P.; Leysen, Josee E. Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 1 p. 71 - 74]
[Shevchenko, Nikolay E.; Nenajdenko, Valentine G.; Balenkova, Elizabeth S. Synthesis, 2003 , # 8 p. 1191 - 1200]