메뉴 건너뛰기




Volumn 66, Issue 34, 2010, Pages 6832-6841

Divergent base-induced reactivity of cycloalkenyl-1-diazenes

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXY HYDROCINNOLINE DERIVATIVE; 4 ALLYL 4A ETHYL 2 (ANILINOCARBONYL) 3 HYDROXY 3 METHYL 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLATE; 4 ALLYL 4A ETHYL 2 (ANILINOCARBONYL) 3 METHYL 5,6,7,8 TETRAHYDROCINNOLINE 4,4A(2H) DICARBOXYLATE; 4 BENZYL 4A ETHYL 2 (AMINOCARBONYL) 3 HYDROXY 3 METHYL 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLATE; 4 BENZYL 4A ETHYL 2 (ANILINOCARBONYL) 3 HYDROXY 3 METHYL 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLATE; 4 BENZYL 4A ETHYL 2 (ANILINOCARBONYL) 3 METHYL 5,6,7,8 TETRAHYDROCINNOLINE 4,4A(2H) DICARBOXYLATE; 4 TERT BUTYL 4A ETHYL 2 (ANILINOCARBONYL) 3 HYDROXY 3 METHYL 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLATE; 4 TERT BUTYL 4A ETHYL 2 (ANILINOCARBONYL) 3 METHYL 5,6,7,8 ETRAHYDROCINNOLINE 4,4A(2H) DICARBOXYLATE; 4A ETHYL 4 (2 METHOXYETHYL) 2 (AMINOCARBONYL) 3 HYDROXY 3 METHYL 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLATE; 4A ETHYL 4 METHYL 2 (AMINOCARBONYL) 3 HYDROXY 3 METHYL 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLAT; 4A ETHYL 4 METHYL 2 (AMINOCARBONYL) 3 HYDROXY 3,7 DIMETHYL 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLATE; ALKENYL GROUP; ALLYL 2 (ANILINOCARBONYL) 3 HYDROXY 3 METHYL 2,3,4,4A,5,6,7,8 OCTAHYDROCINNOLINE 4 CARBOXYLATE; ALLYL 2 (ANILINOCARBONYL) 3 METHYL 2,4A,5,6,7,8 HEXAHYDROCINNOLINE 4 CARBOXYLATE; ALLYL 3 METHYL 2,4A,5,6,7,8 HEXAHYDROCINNOLINE 4 CARBOXYLATE; ALLYL 3 METHYL 5,6,7,8 TETRAHYDROCINNOLINE 4 CARBOXYLATE; BETA OXOCARBOXYLIC ACID ESTER; CYCLOALKENYL 1 DIAZENE DERIVATIVE; DIETHYL 2 (ANILINOCARBONYL) 3 ETHYL 5,6,7,8 TETRAHYDROCINNOLINE 4,4A(2H) DICARBOXYLATE; DIETHYL 2 (ANILINOCARBONYL) 3 HYDROXY 3 (4 NITROPHENYL) 3,4,5,6,7,8 HEXAHYDROCINNOLINE 4 4A(2H) DICARBOXYLATE; DIETHYL 2 (ANILINOCARBONYL) ETHYL 3 HYDROXY 3,4,5,6,7,8 HEXAHYDROCINNOLINE; ETHYL 2 (ANILINOCARBONYL) 3 HYDROXY 3 METHYL 2,3,4,4A,5,6,7,8 OCTAHYDROCINNOLINE 4 CARBOXYLATE; ETHYL 2 (ANILINOCARBONYL) 3 METHYL 2,4A,5,6,7,8 HEXAHYDROCINNOLINE 4 CARBOXYLATE; ETHYL 2 [2 (AMINOCARBONYL)HYDRAZONO] 1 {1 [(2 METHOXYETHYLCARBONYL]-2-OXOPROPYL}CYCLOPENTANECARBOXYLATE; ETHYL 3 METHYL 2,4A,5,6,7,8 HEXAHYDROCINNOLINE 4 CARBOXYLATE; METHYL 2 (ANILINOCARBONYL) 3 HYDROXY 3 METHYL 2,3,4,4A,5,6,7,8 OCTAHYDROCINNOLINE 4 CARBOXYLATE; METHYL 2 (ANILINOCARBONYL) 3 METHYL 2,4A,5,6,7,8 HEXAHYDROCINNOLINE 4 CARBOXYLATE; METHYL 3 METHYL 2,4A,5,6,7,8 HEXAHYDROCINNOLINE 4 CARBOXYLATE; METHYL 3 METHYL 5,6,7,8 TETRAHYDROCINNOLINE 4 CARBOXYLATE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 77955467598     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.06.061     Document Type: Article
Times cited : (7)

References (56)
  • 1
    • 84944056338 scopus 로고    scopus 로고
    • Pyridazines and their Benzo Derivatives
    • W.J. Coates Pyridazines and their Benzo Derivatives A.R. Katrizky, C.W. Rees, E.F.V. Scriven, Comprehensive Heterocyclic Chemistry II Vol. 6 1996 Pergamon Oxford 1 91
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.6 , pp. 1-91
    • Coates, W.J.1
  • 6
    • 0027028719 scopus 로고
    • Pharmacologically Active Pyridazine Derivatives. Part 2
    • G. Heinisch, and H. Kopelent-Frank Pharmacologically Active Pyridazine Derivatives. Part 2 G.P. Ellis, D.K. Luscombe, Progress in Medicinal Chemistry Vol. 29 1992 Elsevier Science B.V. Amsterdam 141 183
    • (1992) Progress in Medicinal Chemistry , vol.29 , pp. 141-183
    • Heinisch, G.1    Kopelent-Frank, H.2
  • 14
    • 0001021307 scopus 로고
    • J.G. Schantl H. Kropf, E. Schaumann, Houben-Weyl Vol. E15 1990 Thieme Stuttgart 909 1100
    • (1990) Houben-Weyl , vol.15 , pp. 909-1100
    • Schantl, J.G.1
  • 32
    • 77955466398 scopus 로고    scopus 로고
    • note
    • 23 Both compounds crystallize in the triclinic crystal system, P-1 space group, with one molecule that constitutes the asymmetric unit. CCDC-761530 and CCDC-761531 contain the supplementary crystallographic data for compounds 5h and 5a, respectively, described in this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.