Arylchlorocarbenes in the synthesis of heterocycles containing two nitrogen atoms

Chemical Communications

Volumn , Issue 13, 2000, Pages 1147-1148

  Romashin, Yuri N ^b   Liu, Michael T H ^b   Nijjar, Satnam S ^b   Attanasi, Orazio A ^a  

^a UNIVERSITY OF URBINO   (Italy)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROCARBON; CARBENE; HETEROCYCLIC COMPOUND; NITROGEN DERIVATIVE; PYRAZOLE DERIVATIVE; PYRROLOPYRIMIDINE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; SYNTHESIS;

EID: 0034617023     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b002940h     Document Type: Article

References (19)

1. M. T. H. Liu, Yu. N. Romashin and R. Bonneau, Int. J. Chem. Kinet., 1994, 26, 1179; R. Bonneau, Yu. N. Romashin, M. T. H. Liu and S. E. MacPherson, J. Chem. Soc., Chem. Commun., 1994, 509.
2. M. T. H. Liu, Yu. N. Romashin and R. Bonneau, Int. J. Chem. Kinet., 1994, 26, 1179; R. Bonneau, Yu. N. Romashin, M. T. H. Liu and S. E. MacPherson, J. Chem. Soc., Chem. Commun., 1994, 509.
3. Yu. N. Romashin, M. T. H. Liu and R. Bonneau, Chem. Commun., 1999, 447; R. Bonneau, Yu. N. Romashin and M. T. H. Liu, J. Photochem. Photobiol., A, 1999, 126, 31; Yu. N. Romashin, M. T. H. Liu, W. Ma and R. A. Moss, Tetrahedron Lett., 1999, 40, 7163.
4. Yu. N. Romashin, M. T. H. Liu and R. Bonneau, Chem. Commun., 1999, 447; R. Bonneau, Yu. N. Romashin and M. T. H. Liu, J. Photochem. Photobiol., A, 1999, 126, 31; Yu. N. Romashin, M. T. H. Liu, W. Ma and R. A. Moss, Tetrahedron Lett., 1999, 40, 7163.
5. Yu. N. Romashin, M. T. H. Liu and R. Bonneau, Chem. Commun., 1999, 447; R. Bonneau, Yu. N. Romashin and M. T. H. Liu, J. Photochem. Photobiol., A, 1999, 126, 31; Yu. N. Romashin, M. T. H. Liu, W. Ma and R. A. Moss, Tetrahedron Lett., 1999, 40, 7163.
6. E. L. Moyano, G.I. Yranzo and J. Elguero, J. Org. Chem., 1998, 63, 8188.
7. D. A. Maiboroda, E. V. Babaev and K. Jug, J. Org. Chem., 1997, 62, 7100.
8. J. M. Minguez, M. I. Castellote, J. J. Vaquero, J. L. Garcia-Navio, J. Alvarez-Builla, O. Castaño and J. L. Andres, J. Org. Chem., 1996, 61, 4655.
9. J. L. Wong, S. M. Brown and H. Rapoport, J. Org. Chem, 1965, 30, 2398.
10. W. H. Graham, J. Am. Chem. Soc., 1965, 87, 4396.
11. B. F. Bonini, G. Maccagnani, G. Mazzanti, G. Rosini and E. Foresti, J. Chem. Soc., Perkin Trans. 1, 1981, 2322.
12. O. A. Attanasi and P. Filippone, Synlett, 1977, 1128; A. Attanasi, P. Filippone, C. Fiorucci, E. Foresti and F. Mantellini, J. Org. Chem., 1998, 63, 9880; O. A. Attanasi, P. Filippone, C. Fiorucci and F. Mantellini, Tetrahedron Lett., 1999, 40, 3891.
13. O. A. Attanasi and P. Filippone, Synlett, 1977, 1128; A. Attanasi, P. Filippone, C. Fiorucci, E. Foresti and F. Mantellini, J. Org. Chem., 1998, 63, 9880; O. A. Attanasi, P. Filippone, C. Fiorucci and F. Mantellini, Tetrahedron Lett., 1999, 40, 3891.
14. O. A. Attanasi and P. Filippone, Synlett, 1977, 1128; A. Attanasi, P. Filippone, C. Fiorucci, E. Foresti and F. Mantellini, J. Org. Chem., 1998, 63, 9880; O. A. Attanasi, P. Filippone, C. Fiorucci and F. Mantellini, Tetrahedron Lett., 1999, 40, 3891.
15. C. G. Overberger and I. C. Kogon, J. Am. Chem. Soc., 1954, 76, 1879.
16. H.-H. Perkampus and Th. Bluhm, Tetrahedron, 1972, 28, 2099.
17. pyr); MS: m/z 306 (33), 304 (100).
18. M. E. Kuehne, S. J. Weaver and P. Franz, J. Org. Chem., 1964, 29, 1582.
19. 2, 0.468% Xe, and 99.334% Ne. The sample in a 10 × 10 mm cell was excited at 351 nm by single light pulses (10 ns; 40 mJ). The detection unit comprised a 1000 W Oriel xenon arc lamp, a 1 in. Uniblitz shutter, Instruments SA grating monochromator, and a RCA 4840 photo-multiplier tube wired in a 5-dynode configuration. The data collection and analysis system included a Stanford Research Systems model DG535 4-channel digital delay/pulse generator and a Tektronix TDS 320 2-channel oscilloscope.