Microwave-accelerated coupling-isomerization-enamine addition-aldol condensation sequences to 1-acetyl-2-amino-cyclohexa-1,3-dienes

Synlett

Volumn , Issue 12, 2006, Pages 1841-1846

  Schramm, Oana G ^a   Müller, Thomas J J ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Alkynes; Condensations; Cross couplings; Cyclizations; Microwave reactions

Indexed keywords

1 ACETYL 2 AMINO CYCLOHEXA 1,3 DIENE DERIVATIVE; CYCLOHEXANE DERIVATIVE; ENAMINE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; ELECTRON; ISOMERIZATION;

EID: 33747061572     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-947352     Document Type: Article

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40. 3O (457.6): C, 81.40; H, 5.91; N, 9.19. Found: C, 81.02; H, 6.05; N, 9.09.
41. All compounds have been fully characterized spectroscopically and by correct elemental analysis or HRMS, respectively.
42. Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication nos. CCDC-605608 (7a), and CCDC-605609 (9d). Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [Fax: +44 (1223)336-033; email: deposit@ccdc.cam.ac.uk].
43. 2 (344.4): C, 76.72; H, 5.85; N, 8.13. Found: C, 76.96; H, 5.89; N, 8.15.