An asymmetry induced azepine-ring formation through the ene reactions at the periphery of heterocyclic systems

Tetrahedron

Volumn 52, Issue 41, 1996, Pages 13111-13120

  Noguchi, Michihiko ^a   Mizukoshi, Takashi ^a   Nakagawa, Shinya ^a   Kakehi, Akikazu ^b  

^a YAMAGUCHI UNIVERSITY   (Japan)

^b SHINSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 OXAZINE DERIVATIVE; AZEPINE DERIVATIVE;

ARTICLE; CALCULATION; CHIRALITY; DRUG SYNTHESIS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0030272309     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00773-9     Document Type: Article

References (14)

1. (1) Noguchi, M.; Mizukoshi, T.; Kakehi, A. Tetrahedron in the preceeding paper.
2. (2) Noguchi, M.; Mizukoshi, T.; Uchida, T.; Kuroki, Y. Tetrahedron in the preceding paper.
3. (3) Kuroki, Y.; Akao, R.; Inazumi, T.; Noguchi, M. Tetrahedron 1994, 50, 1063.
4. -1 would be required to recoil the helical structure of the "Intermediate".
5. (5) Mile, N. J.; Sammes, P. G. J. Chem. Soc., Perkin Trans. 1 1985, 2299; Fujii, T.; Ohba, M.; Sakari, M.; Matsubara, S. Chem. Pharm. Bull. 1990, 38, 2702; Schmidt, C.; Chishti, N. H.; Brening, T. Synthesis 1982, 391.
6. (5) Mile, N. J.; Sammes, P. G. J. Chem. Soc., Perkin Trans. 1 1985, 2299; Fujii, T.; Ohba, M.; Sakari, M.; Matsubara, S. Chem. Pharm. Bull. 1990, 38, 2702; Schmidt, C.; Chishti, N. H.; Brening, T. Synthesis 1982, 391.
7. (5) Mile, N. J.; Sammes, P. G. J. Chem. Soc., Perkin Trans. 1 1985, 2299; Fujii, T.; Ohba, M.; Sakari, M.; Matsubara, S. Chem. Pharm. Bull. 1990, 38, 2702; Schmidt, C.; Chishti, N. H.; Brening, T. Synthesis 1982, 391.
8. (6) George, T.; Mehta, D. V.; Dabholkar, D. A. J. Org. Chem. 1971, 36, 2192.
9. (7) Butt, M. A.; Elvidge, J. A. J. Chem. Soc. 1963, 4483.
10. (8) Senda, S.; Hirota, G.; Yang, G. N.; Shiraishi, M. Yakugaku Zasshi 1971, 91, 1372.
11. (9) The authors have deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained on request from the Director, Cambridge Crystallographic Centre, University Chemical Labratory, Lensfield Road, Cambridge CB2 1EW, U. K.
12. (10) TEXSAN TEXRAY, Structure Analysis Package, Molecular Structures Corporation, 1985.
13. (11) Gilmore, C. J. J. Appl. Crystallogr. 1984, 17, 42.
14. (12) Johnson, C. K.; ORTEP II, Report ORNL-5138, Oak Ridge National Laboratory, Oak Ridge, Tennessee, 1976.