-
1
-
-
0010319687
-
-
Venice, Italy, June 28-July 2, Book of Abstracts
-
1. Presented at the 12th International Conference on Organic Synthesis, Venice, Italy, June 28-July 2, 1998, Book of Abstracts, p 405.
-
(1998)
12th International Conference on Organic Synthesis
, pp. 405
-
-
-
2
-
-
84943382356
-
-
Bird, C. W.; Cheeseman, G. W. H., Eds.; Pergamon Press: Oxford
-
2. a) Dean, F. M.; Sargent, M. V. in Comprehensive Heterocyclic Chemistry; Bird, C. W.; Cheeseman, G. W. H., Eds.; Pergamon Press: Oxford, 1984; Vol. 4, pp 531-598.
-
(1984)
Comprehensive Heterocyclic Chemistry
, vol.4
, pp. 531-598
-
-
Dean, F.M.1
Sargent, M.V.2
-
5
-
-
0030845835
-
-
d) Kappe, C. O.; Murphree, S. S.; Padwa, A. Tetrahedron 1997, 53, 14179-14233.
-
(1997)
Tetrahedron
, vol.53
, pp. 14179-14233
-
-
Kappe, C.O.1
Murphree, S.S.2
Padwa, A.3
-
9
-
-
0000048258
-
-
Trost, B. M.; Fleming, I.; Paquette, L. A., Eds.; Pergamon Press: Oxford
-
d) For a comprehensive treatment of intermolecular [4+2] cycloadditions: Oppolzer, W. in Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Paquette, L. A., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, pp 315-399.
-
(1991)
Comprehensive Organic Synthesis
, vol.5
, pp. 315-399
-
-
Oppolzer, W.1
-
12
-
-
0001639102
-
-
g) Fraile, J. M.; García, J. I.; Gracia, D.; Mayoral, J. A.; Pires, E. J. Org. Chem. 1996, 61, 9479-9482.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 9479-9482
-
-
Fraile, J.M.1
García, J.I.2
Gracia, D.3
Mayoral, J.A.4
Pires, E.5
-
13
-
-
0010318506
-
-
4. A recent semiempirical study has been undertaken to rationalize why catalytic quantities of Lewis acid are more effective than stoichiometric ones in intramolecular cycloadditions with furans: Hunt, I. R.; Rauk, A.; Keay, B. A. J. Org. Chem. 1996, 61, 751-757.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 751-757
-
-
Hunt, I.R.1
Rauk, A.2
Keay, B.A.3
-
15
-
-
0000362698
-
-
b) Kotsuki, H.; Nishizawa, H.; Ochi, M.; Matsuoka, K. Bull. Chem. Soc. Jpn. 1982, 55, 496-499.
-
(1982)
Bull. Chem. Soc. Jpn.
, vol.55
, pp. 496-499
-
-
Kotsuki, H.1
Nishizawa, H.2
Ochi, M.3
Matsuoka, K.4
-
18
-
-
0029919983
-
-
e) Dauben, W. G.; Lam, J. Y. L.; Guo, Z. R. J. Org. Chem. 1996, 61, 4816-4819.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 4816-4819
-
-
Dauben, W.G.1
Lam, J.Y.L.2
Guo, Z.R.3
-
20
-
-
37049071711
-
-
b) Adams, J. M.; Dyer, S.; Martin, K.; Matear, W. A.; McCabe, R. W. J. Chem. Soc., Perkin Trans. 1 1994, 761-765.
-
(1994)
J. Chem. Soc., Perkin Trans. 1
, pp. 761-765
-
-
Adams, J.M.1
Dyer, S.2
Martin, K.3
Matear, W.A.4
McCabe, R.W.5
-
21
-
-
0032473907
-
-
7. Avalos, M.; Babiano, R.; Bravo, J. L.; Cintas, P.; Jiménez, J. L.; Palacios, J. C.; Ranu, B. C. Tetrahedron Lett. 1998, 39, 2013-2016.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2013-2016
-
-
Avalos, M.1
Babiano, R.2
Bravo, J.L.3
Cintas, P.4
Jiménez, J.L.5
Palacios, J.C.6
Ranu, B.C.7
-
23
-
-
0030022958
-
-
2O, 130 °C): Cattalini, M.; Cossu, S.; Fabris, F.; De Lucchi, O. Synth. Commun. 1996, 26, 637-647.
-
(1996)
Synth. Commun.
, vol.26
, pp. 637-647
-
-
Cattalini, M.1
Cossu, S.2
Fabris, F.3
De Lucchi, O.4
-
24
-
-
0010318507
-
-
note
-
10. Microwave-assisted reactions were conducted in a domestic oven (2.45 GHz, 150 W) as well as in a monomode microwave reactor with focused electromagnetic field (Synthewave 402, Prolabo: 2.45 GHz, 300 W, 5% relative intensity).
-
-
-
-
26
-
-
0030793981
-
-
2, r.t., 90 h) to afford Diels-Alder adducts: Maggiani, A.; Tubul, A.; Brun, P. Synthesis 1997, 631-633.
-
(1997)
Synthesis
, pp. 631-633
-
-
Maggiani, A.1
Tubul, A.2
Brun, P.3
|