Concise synthesis of fused polycyclic quinolines

Tetrahedron Letters

Volumn 42, Issue 22, 2001, Pages 3705-3708

  Rossi, Elisabetta ^a   Abbiati, Giorgio ^a   Arcadi, Antonio ^b   Marinelli, Fabio ^b  

^a UNIVERSITY OF MILAN   (Italy)

^b UNIVERSITY OF L'AQUILA   (Italy)

Author keywords

2+2 cycloadditions; Polycyclic quinolines; Tandem reactions

Indexed keywords

BETA (2 AMINOPHENYL) ALPHA,BETA YNONE DERIVATIVE; BICYCLO[4.2.0]OCTANE[7,8 C] 2 QUINOLINE DERIVATIVE; ENAMINE; KETONE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; REACTION ANALYSIS; STOICHIOMETRY; SYNTHESIS;

EID: 0035963062     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)00553-6     Document Type: Article

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23. 3): δ 18.90 and 19.53 (C3′/C4′), 24.40 (2C, N-C-C̄), 25.49 (C2′/C5′), 29.88 (C2′/C5′), 40.98 (C6′), 47.94 (2C, N-C), 70.11 (C1′), 123.08 (C7), 124.69 (quat. C), 126.78 (C6), 129.34 (C2′′, C6′′ and C5), 130.50 (C3′′ and C5′′), 131.41 (C8), 136.08, 136.31, 148.27, 151.83 and 153.34 (quat. C).
24. 3): δ 23.25 (C9), 24.94 (2C, N-C-C̄), 25.98 (C10), 34.97 (C11), 48.03 (2C, N-C), 98.53 (C8), 124.22 (C1), 126.83 (C2/C3), 127.73 (2C, C3′, C5′), 129.50 (C2/C3), 130.13 (2C, C2′, C6′), 130.64 (C4), 126.52, 129.32, 134.26, 140.41, 144.57, 147.50, 148.19, 156.06 (quat. C).
25. Cook, A. G. In Enamines: Synthesis, Structure, and Reaction, 2nd ed.; Cook, A. G. Ed.; Marcel Dekker: New York, 1988; Chapter 1, pp. 1-27.