-
2
-
-
0037182721
-
-
(a) Ghorai, B. K.; Menon, S.; Johnson, D. L.; Herndon, J. W. Org. Lett. 2002, 4, 2121-2124.
-
(2002)
Org. Lett.
, vol.4
, pp. 2121-2124
-
-
Ghorai, B.K.1
Menon, S.2
Johnson, D.L.3
Herndon, J.W.4
-
5
-
-
0023692505
-
-
(a) Wulff, W. D.; McCallum, J. S.; Kunng, F. A. J. Am. Chem. Soc. 1988, 110, 7419-7434.
-
(1998)
J. Am. Chem. Soc.
, vol.110
, pp. 7419-7434
-
-
Wulff, W.D.1
McCallum, J.S.2
Kunng, F.A.3
-
6
-
-
0037140873
-
-
(b) Anderson, J. C.; Cran, J. W.; King, N. P. Tetrahedron Lett. 2002, 43, 3849-3852.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 3849-3852
-
-
Anderson, J.C.1
Cran, J.W.2
King, N.P.3
-
7
-
-
0001171813
-
-
note
-
There are numerous examples of successful formation of carbonyl ylides from diazo compounds that contain pendant esters; however formation of a carbonyl ylide from a pendant ketone is easier than from an ester. Padwa, A.; Hornbuckle, S. F.; Fryxell, G. E.; Stull, P. D. J. Org. Chem. 1989, 54, 817-824.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 817-824
-
-
Padwa, A.1
Hornbuckle, S.F.2
Fryxell, G.E.3
Stull, P.D.4
-
10
-
-
0032564643
-
-
(a) Bernab, P.; Castedo, L.; Dominguez, D. Tetrahedron Lett. 1998, 39, 9785-9788.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 9785-9788
-
-
Bernab, P.1
Castedo, L.2
Dominguez, D.3
-
11
-
-
33746573760
-
-
(b) Peters, O.; Debaerdemaeker, T.; Friedrichsen, W. J. Chem. Soc., Perkin Trans. 1 1999, 59-70.
-
(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 59-70
-
-
Peters, O.1
Debaerdemaeker, T.2
Friedrichsen, W.3
-
12
-
-
0028818649
-
-
(c) Kappe, C. O.; Cochran, J. E.; Padwa, A. Tetrahedron Lett. 1995, 36, 9285-9288.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 9285-9288
-
-
Kappe, C.O.1
Cochran, J.E.2
Padwa, A.3
-
14
-
-
0037060063
-
-
(e) Sarkar, T. K.; Basak, S.; Panda, N. Tetrahedron Lett. 2002, 43, 1341-1344.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 1341-1344
-
-
Sarkar, T.K.1
Basak, S.2
Panda, N.3
-
15
-
-
0034685856
-
-
(f) Sarkar, T. K.; Ghosh, S. K.; Chow, T. J. J. Org. Chem. 2000, 65, 3111-3115.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3111-3115
-
-
Sarkar, T.K.1
Ghosh, S.K.2
Chow, T.J.3
-
16
-
-
0034728158
-
-
(g) Sarkar, T. K.; Basak, S.; Ghosh, S. K. Tetrahedron Lett. 2000, 41, 759-762.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 759-762
-
-
Sarkar, T.K.1
Basak, S.2
Ghosh, S.K.3
-
18
-
-
0001685757
-
-
For pioneering work in the development of this approach to carbene complex synthesis, see: (a) Semmelhack, M. F.; Lee, G. R. Organometallics 1987, 6, 1839-44.
-
(1987)
Organometallics
, vol.6
, pp. 1839-1844
-
-
Semmelhack, M.F.1
Lee, G.R.2
-
19
-
-
0000151160
-
-
(b) Schwindt, M. A.; Lejon, T.; Hegedus, L. S. Organometallics 1990, 9, 2814-2819.
-
(1990)
Organometallics
, vol.9
, pp. 2814-2819
-
-
Schwindt, M.A.1
Lejon, T.2
Hegedus, L.S.3
-
20
-
-
0035819649
-
-
note
-
This idea was inspired by recent successes in transferring the carbene unit of Fischer carbene complexes to other metals. (a) Sierra, M. A.; del Amo, J. C.; Mancheño, M. J.; Gómez-Gallego, M. J. Am. Chem. Soc. 2001, 123, 851-861.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 851-861
-
-
Sierra, M.A.1
Del Amo, J.C.2
Mancheño, M.J.3
Gómez-Gallego, M.4
-
21
-
-
0036971977
-
-
(b) Sierra, M. A.; del Amo, J. C.; Mancheno, M. J.; Gomez-Gallego, M.; Torres, M. R. Chem. Commun. 2002, 1842-1843.
-
(2002)
Chem. Commun.
, pp. 1842-1843
-
-
Sierra, M.A.1
Del Amo, J.C.2
Mancheno, M.J.3
Gomez-Gallego, M.4
Torres, M.R.5
-
22
-
-
0035817673
-
-
(c) Goettker-Schnetmann, I.; Aumann, R.; Bergander, K. Organometallics 2001, 20, 3574-3581.
-
(2001)
Organometallics
, vol.20
, pp. 3574-3581
-
-
Goettker-Schnetmann, I.1
Aumann, R.2
Bergander, K.3
-
24
-
-
0035903612
-
-
(e) Barluenga, J.; Lopez, L. A.; Lober, O.; Tomas, M.; Garcia-Granda, S.; Alvarez-Rua, C.; Borge, J. Angew. Chem., Int. Ed. 2001, 40, 3392-3394.
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 3392-3394
-
-
Barluenga, J.1
Lopez, L.A.2
Lober, O.3
Tomas, M.4
Garcia-Granda, S.5
Alvarez-Rua, C.6
Borge, J.7
-
26
-
-
0000411634
-
-
note
-
We are not aware of an exhaustive study of the relative reactivity; however in a study of intramolecular cyclopropanation by chromium carbene complexes, all alkene substitution patterns appear to be tolerated. Soderberg, B. C.; Hegedus, L. S. Organometallics 1990, 9, 3113-3121.
-
(1990)
Organometallics
, vol.9
, pp. 3113-3121
-
-
Soderberg, B.C.1
Hegedus, L.S.2
-
27
-
-
0024803676
-
-
note
-
The exo Diels-Alder adduct has been depicted and is anticipated on the basis of literature precedent. (a) Meegalla, S. K.; Rodrigo, R. Synthesis 1989, 942-944.
-
(1989)
Synthesis
, pp. 942-944
-
-
Meegalla, S.K.1
Rodrigo, R.2
-
28
-
-
0000168987
-
-
(b) Yamaguchi, Y.; Yamada, H.; Hayakawa, K.; Kanematsu, K. J. Org. Chem. 1987, 52, 2040-2046.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 2040-2046
-
-
Yamaguchi, Y.1
Yamada, H.2
Hayakawa, K.3
Kanematsu, K.4
-
30
-
-
0001716827
-
-
note
-
Related Diels-Alder reactions have produced mixtures of 22 and 14. (a) Chen, C. W.; Beak, P. J. Org. Chem. 1986, 51, 3325-3334.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 3325-3334
-
-
Chen, C.W.1
Beak, P.2
-
32
-
-
0001766959
-
-
note
-
The amide carbonyl group is more stable than the aldehyde or ketone carbonyl group. Wiberg, K. B.; Hadad, C. M.; Rablen, P. R.; Cioslowski, J. J. Am. Chem. Soc. 1992, 114, 8644-8654.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 8644-8654
-
-
Wiberg, K.B.1
Hadad, C.M.2
Rablen, P.R.3
Cioslowski, J.4
-
35
-
-
0001442424
-
-
Hegedus, L. S.; McGuire, M. A.; Schultze, L. M. Org. Synth. 1987, 65, 140-145.
-
(1987)
Org. Synth.
, vol.65
, pp. 140-145
-
-
Hegedus, L.S.1
McGuire, M.A.2
Schultze, L.M.3
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