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3
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85031058645
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in press
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Lavilla, R.; Carranco, I.; Díaz, J. L.; Bernabeu, M. C.; de la Rosa, G. Mol. Diversity, in press.
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Mol. Diversity
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Lavilla, R.1
Carranco, I.2
Díaz, J.L.3
Bernabeu, M.C.4
De La Rosa, G.5
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4
-
-
0029135125
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-
For evidence on the stepwise mechanism of the formal [4+2] cycloadditions involving anilines, aldehydes and olefins, see: (a) Kobayashi, S.; Ishitani, H.; Nagayama, S. Synthesis 1995, 1195-1202; (b) Sartori, G.; Bigi, F.; Maggi, R.; Mazzacani, A.; Oppici, G. Eur. J. Org. Chem. 2001, 2513-2518; (c) Hermitage, S.; Jay, D. A.; Whiting, A. Tetrahedron Lett. 2002, 43, 9633-9636; (d) Also see Ref. 2.
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(1995)
Synthesis
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Kobayashi, S.1
Ishitani, H.2
Nagayama, S.3
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5
-
-
0034952519
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-
For evidence on the stepwise mechanism of the formal [4+2] cycloadditions involving anilines, aldehydes and olefins, see: (a) Kobayashi, S.; Ishitani, H.; Nagayama, S. Synthesis 1995, 1195-1202; (b) Sartori, G.; Bigi, F.; Maggi, R.; Mazzacani, A.; Oppici, G. Eur. J. Org. Chem. 2001, 2513-2518; (c) Hermitage, S.; Jay, D. A.; Whiting, A. Tetrahedron Lett. 2002, 43, 9633-9636; (d) Also see Ref. 2.
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(2001)
Eur. J. Org. Chem.
, pp. 2513-2518
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Sartori, G.1
Bigi, F.2
Maggi, R.3
Mazzacani, A.4
Oppici, G.5
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6
-
-
0037164629
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-
For evidence on the stepwise mechanism of the formal [4+2] cycloadditions involving anilines, aldehydes and olefins, see: (a) Kobayashi, S.; Ishitani, H.; Nagayama, S. Synthesis 1995, 1195-1202; (b) Sartori, G.; Bigi, F.; Maggi, R.; Mazzacani, A.; Oppici, G. Eur. J. Org. Chem. 2001, 2513-2518; (c) Hermitage, S.; Jay, D. A.; Whiting, A. Tetrahedron Lett. 2002, 43, 9633-9636; (d) Also see Ref. 2.
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(2002)
Tetrahedron Lett.
, vol.43
, pp. 9633-9636
-
-
Hermitage, S.1
Jay, D.A.2
Whiting, A.3
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7
-
-
85031053757
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-
Also see Ref. 2
-
For evidence on the stepwise mechanism of the formal [4+2] cycloadditions involving anilines, aldehydes and olefins, see: (a) Kobayashi, S.; Ishitani, H.; Nagayama, S. Synthesis 1995, 1195-1202; (b) Sartori, G.; Bigi, F.; Maggi, R.; Mazzacani, A.; Oppici, G. Eur. J. Org. Chem. 2001, 2513-2518; (c) Hermitage, S.; Jay, D. A.; Whiting, A. Tetrahedron Lett. 2002, 43, 9633-9636; (d) Also see Ref. 2.
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-
-
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8
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85031059827
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note
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0): 290 (4.2).
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-
-
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9
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85031058942
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note
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0): 271 (4.2).
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11
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85031051164
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Spartan'02 Wavefunction, Inc. Irvine, CA
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Spartan'02 Wavefunction, Inc. Irvine, CA.
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15
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0002505951
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Part 2; Patai, S., Ed.; Wiley: New York
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(a) Duhamel, L. In The Chemistry of Functional Groups, Supplement F, Part 2; Patai, S., Ed.; Wiley: New York, 1982; pp. 849-907.
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(1982)
The Chemistry of Functional Groups
, Issue.SUPPL. F
, pp. 849-907
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Duhamel, L.1
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16
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0034660255
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For recent results, see: (b) Lavilla, R.; Kumar, R.; Coll, O.; Masdeu, C.; Spada, A.; Bosch, J.; Espinosa, E.; Molins, E. Chem. Eur. J. 2000, 6, 1763-1772; (c) Simon, C.; Peyronel, J.-F.; Rodriguez, J. Org. Lett. 2001, 3, 2145-2148.
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(2000)
Chem. Eur. J.
, vol.6
, pp. 1763-1772
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Lavilla, R.1
Kumar, R.2
Coll, O.3
Masdeu, C.4
Spada, A.5
Bosch, J.6
Espinosa, E.7
Molins, E.8
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17
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0035850297
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For recent results, see: (b) Lavilla, R.; Kumar, R.; Coll, O.; Masdeu, C.; Spada, A.; Bosch, J.; Espinosa, E.; Molins, E. Chem. Eur. J. 2000, 6, 1763-1772; (c) Simon, C.; Peyronel, J.-F.; Rodriguez, J. Org. Lett. 2001, 3, 2145-2148.
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(2001)
Org. Lett.
, vol.3
, pp. 2145-2148
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Simon, C.1
Peyronel, J.-F.2
Rodriguez, J.3
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18
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85031061144
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In sharp contrast, the analogous process with anilines gives a mixture of epimers at the ester α-position
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In sharp contrast, the analogous process with anilines gives a mixture of epimers at the ester α-position.
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21
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0032077266
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(c) For a recent result, see: Shen, Z.; Eisenreich, W.; Kutchan, T. I. Phytochemistry 1998, 48, 293-296.
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(1998)
Phytochemistry
, vol.48
, pp. 293-296
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Shen, Z.1
Eisenreich, W.2
Kutchan, T.I.3
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