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Volumn 75, Issue 12, 2010, Pages 1033-1038

Chlorotrimethylsilane-promoted one-pot synthesis of steroidal[17,16-d] pyrimidines

Author keywords

Biginelli type reaction; Pyrimidine; Steroid 17 ones; Steroidal 17,16 d pyrimidines; TMSCl

Indexed keywords

10 HYDROXY 12 (4 METHOXYPHENYL) 6A,8A DIMETHYL 2,2A,3,4,5,6,6A,6B,7,8,8A,13,13A,13B TETRADECAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 10 HYDROXY 6A,8A DIMETHYL 12 (2 NITROPHENYL) 2,2A,3,4,5,6,6A,6B,7,8,8A,13,13A,13B TETRADECAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 10 HYDROXY 6A,8A DIMETHYL 12 (3 NITROPHENYL) 2,2A,3,4,5,6,6A,6B,7,8,8A,13,13A,13B TETRADECAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 10 HYDROXY 6A,8A DIMETHYL 2 PHENYL 3,4,5,6,6A,6B,7,8,8A,13,13A,13B DODECAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 10 HYDROXY DIMETHYL 12 PHENYL 2,2A,3,4,5,6,6A,6B,7,8,8A,13,13A,13B TETRADECAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 10 HYDROXY0 12 (4 METHOXYPHENYL) 6A,8A DIMETHYL 3,4,5,6,6A,6B,7,8,8A,13,13A,13B DODECAHYDRO 1H-NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 12 (4 FLUOROPHENYL) 10 HYDROXY 6A,8A DIMETHYL 2,2A,3,4,5,6,6A,6B,7,8,8A,13,13A,13B TETRADECAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 12 (4 FLUOROPHENYL) 10 HYDROXY 6A,8A DIMETHYL 3,4,5,6,6A,6B,7,8,8A,13,13A,13B DODECAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 4 YL ACETATE; 4 METHOXY 12 (4 METHOXYPHENYL) 8A METHYL 2,6B,7,8,8A,13,13A,13B OCTAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 10 OL; 4 METHOXY 8A METHYL 12 PHENYL 2,6B,7,8,8A,13,13A,13B OCTAHYDRO 1H NAPHTHO[2',1':4,5]INDENO[1,2 D]PYRIMIDIN 10 OL; ACETONITRILE; ALDEHYDE; CHLOROTRIMETHYLSILANE; HYDROXYL GROUP; N,N DIMETHYLFORMAMIDE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG; UREA;

EID: 77955925038     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2010.06.007     Document Type: Article
Times cited : (18)

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