Synthesis of the new triheterocyclic system C3N-C4N-C6N.: 3-aryl-2,5,5-trimethyl-9a-methylsulfanyl-9-phenoxy-4,5,6,8,9,9a-hexahydro-3H-azeto[1,2-a]pyrrolo[3,2-c]azepin-8-ones

被引:5
作者
Martínez, R
Avila-Zárraga, JG
López-López, G
Nava-Salgado, VO
机构
[1] Univ Nacl Autonoma Mexico, Inst Quim, Mexico City 04510, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Quim, Mexico City 04510, DF, Mexico
关键词
D O I
10.3987/COM-99-8662
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The regio- and stereoselective synthesis of the cis-3-aryl-2,5,5-trimethyl-9a-methylsulfanyl-9-phenoxy-4,5,6,8,9,9a-hexahydro-3H-azeto[1,2-a]pyrrolo[3,2-c]azepin-8-ones (1) was performed. A four-step sequence, which yields are good, constitutes the first synthetic way for the preparation of the first member of this new C3N-C4N-C6N series.
引用
收藏
页码:557 / +
页数:15
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共 36 条
[1]   Origins of the stereodivergent outcome in the Staudinger reaction between acyl chlorides and imines [J].
Arrieta, A ;
Lecea, B ;
Cossío, FP .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (17) :5869-5876
[2]  
Asseline U, 1997, NEW J CHEM, V21, P5
[3]   ACYCLIC STEREOSELECTION - ERYTHROSELECTIVE ALDOL CONDENSATION OF 4-ACYL-2,3-DIHYDRO-4H-1,4-BENZOTHIAZINE AND 10-ACYLPHENOTHIAZINE [J].
BABUDRI, F ;
DINUNNO, L ;
FLORIO, S .
TETRAHEDRON LETTERS, 1983, 24 (36) :3883-3886
[4]   ENEHYDRAZINES .22. LACTAMS FROM 1,5,6,7-TETRAHYDRO-4H-INDOL-4-ONES [J].
BARDAKOS, V ;
SUCROW, W .
CHEMISCHE BERICHTE-RECUEIL, 1978, 111 (05) :1780-1788
[5]  
BRESLIN HJ, 1995, J MED CHEM, V38, P771, DOI 10.1021/jm00005a005
[6]   ACYCLIC STEREOSELECTION .48. REVERSAL OF STEREOCHEMISTRY IN THE ALDOL REACTIONS OF A CHIRAL BORON ENOLATE [J].
DANDA, H ;
HANSEN, MM ;
HEATHCOCK, CH .
JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (01) :173-181
[7]   ENANTIOSELECTIVE ALDOL CONDENSATIONS .2. ERYTHRO-SELECTIVE CHIRAL ALOL CONDENSATIONS VIA BORON ENOLATES [J].
EVANS, DA ;
BARTROLI, J ;
SHIH, TL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (08) :2127-2129
[8]   INVITRO ASSESSMENT OF N-[2-(DIMETHYLAMINO)ETHYL]ACRIDINE-4-CARBOXAMIDE, A DNA-INTERCALATING ANTITUMOR DRUG WITH REDUCED SENSITIVITY TO MULTIDRUG RESISTANCE [J].
FINLAY, GJ ;
MARSHALL, E ;
MATTHEWS, JHL ;
PAULL, KD ;
BAGULEY, BC .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1993, 31 (05) :401-406
[9]   The novel cyclopropapyrroloindole (CPI) bisalkylators bearing 3,3′-(1,4-phenylene)diacryloyl group as a linker [J].
Fukuda, Y ;
Seto, S ;
Furuta, H ;
Ebisu, H ;
Oomori, Y .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (15) :2003-2004
[10]  
GAJDA T, 1979, SYNTHESIS-STUTTGART, P549