-
1
-
-
0019168718
-
-
(a) Salzmann, T. N.; Ratcliffe, R. W.; Christensen, B. G.; Bouffard, F. A. J. Am. Chem. Soc. 1980, 102, 6161.
-
(1980)
J. Am. Chem. Soc
, vol.102
, pp. 6161
-
-
Salzmann, T.N.1
Ratcliffe, R.W.2
Christensen, B.G.3
Bouffard, F.A.4
-
2
-
-
33748896044
-
-
(b) Aller, E.; Buck, R. T.; Drysdale, M. J.; Ferris, L.; Haigh, D.; Moody, C. J.; Pearson, N. D.; Sanghera, J. B. J. Chem. Soc., Perkin Trans. 1 1996, 2879.
-
(1996)
J. Chem. Soc., Perkin Trans. 1
, pp. 2879
-
-
Aller, E.1
Buck, R.T.2
Drysdale, M.J.3
Ferris, L.4
Haigh, D.5
Moody, C.J.6
Pearson, N.D.7
Sanghera, J.B.8
-
3
-
-
0036431541
-
-
(c) Deng, G.; Jiang, N.; Ma, Z.; Wang, J. Synlett 2002, 1913.
-
(2002)
Synlett
, pp. 1913
-
-
Deng, G.1
Jiang, N.2
Ma, Z.3
Wang, J.4
-
4
-
-
33746329351
-
-
(d) Dong, C.; Deng, G.: Wang, J. J. Org. Chem. 2006, 71, 5560.
-
(2006)
J. Org. Chem
, vol.71
, pp. 5560
-
-
Dong, C.1
Deng, G.2
Wang, J.3
-
5
-
-
0003394220
-
-
For reviews involving catalyzed diazo compound N-H insertion reactions, see: a, Wiley: New York, Chapter 8.2
-
For reviews involving catalyzed diazo compound N-H insertion reactions, see: (a) Doyle, M. P.; McKervey, M. A.; Ye, T. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds; Wiley: New York, 1998; Chapter 8.2.
-
(1998)
Modern Catalytic Methods for Organic Synthesis with Diazo Compounds
-
-
Doyle, M.P.1
McKervey, M.A.2
Ye, T.3
-
7
-
-
0040863866
-
-
For recent examples, see: c
-
For recent examples, see: (c) Hrytsak, M.; Durst, T. Heterocycles 1987, 26, 2393.
-
(1987)
Heterocycles
, vol.26
, pp. 2393
-
-
Hrytsak, M.1
Durst, T.2
-
8
-
-
0036923182
-
-
(d) Morilla, M. E.; Diaz-Requejo, M. M.; Belderrain, T. R.; Nicasio, M. C.; Trofimenko, S.; Perez, P. J. Chem. Commun. 2002, 24, 2998.
-
(2002)
Chem. Commun
, vol.24
, pp. 2998
-
-
Morilla, M.E.1
Diaz-Requejo, M.M.2
Belderrain, T.R.3
Nicasio, M.C.4
Trofimenko, S.5
Perez, P.J.6
-
9
-
-
33645798373
-
-
For example of highly enantioselective metal-catalyzed intermoelcular carbenoid N-H insertion reactions, see
-
(e) Aviv, I.; Gross, Z. Synlett 2006, 6, 951. For example of highly enantioselective metal-catalyzed intermoelcular carbenoid N-H insertion reactions, see:
-
(2006)
Synlett
, vol.6
, pp. 951
-
-
Aviv, I.1
Gross, Z.2
-
10
-
-
34248531594
-
-
(f) Liu, B.; Zhu, S.-F.; Zhang, W.; Chen, C; Zhou, Q.-L. J. Am. Chem. Soc. 2007, 129, 5834.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 5834
-
-
Liu, B.1
Zhu, S.-F.2
Zhang, W.3
Chen, C.4
Zhou, Q.-L.5
-
12
-
-
33748738009
-
-
(a) Galardon, E.; Maux, P. L.; Simonneaux, G. J. Chem. Soc., Perkin Trans. 1 1997, 2455.
-
(1997)
J. Chem. Soc., Perkin Trans. 1
, pp. 2455
-
-
Galardon, E.1
Maux, P.L.2
Simonneaux, G.3
-
13
-
-
0034695585
-
-
(b) Galardon, E.; Maux, P. L.; Simonneaux, G. Tetrahedron 2000, 56, 615.
-
(2000)
Tetrahedron
, vol.56
, pp. 615
-
-
Galardon, E.1
Maux, P.L.2
Simonneaux, G.3
-
14
-
-
0003247210
-
-
J, 3079
-
Zotto, A. D.; Baratta, W.; Rigo, P. ,J. Chem. Soc., Perkm Trans. 1 1999, 3079.
-
(1999)
Chem. Soc., Perkm Trans. 1
-
-
Zotto, A.D.1
Baratta, W.2
Rigo, P.3
-
16
-
-
33746356562
-
-
For catalysts that work in water, see: (a) Candeias, N. R.; Gois. P. M. P.; Afonso,' C. A. M. J. Org. Chem. 2006, 71, 5489.
-
For catalysts that work in water, see: (a) Candeias, N. R.; Gois. P. M. P.; Afonso,' C. A. M. J. Org. Chem. 2006, 71, 5489.
-
-
-
-
18
-
-
33750288947
-
-
(c) Estevan, F.; Lloret. J.; Sanau, M.; Ubeda. A. Organometalltcs 2006, 25, 4977.
-
(2006)
Organometalltcs
, vol.25
, pp. 4977
-
-
Estevan, F.1
Lloret, J.2
Sanau, M.3
Ubeda, A.4
-
20
-
-
0041878773
-
-
For the literatures on the reactivity of different carbenoids, see: a
-
For the literatures on the reactivity of different carbenoids, see: (a) Davies, H. M. L.; Beckwith. R. E. J. Chem. Rev. 2003, 103, 2861.
-
(2003)
Chem. Rev
, vol.103
, pp. 2861
-
-
Davies, H.M.L.1
Beckwith, R.E.J.2
-
22
-
-
58149193971
-
-
http://www.chem.wisc.edu/areas/reicli/pkatable.
-
-
-
-
23
-
-
0001060227
-
-
For examples of rhodium-catalyzed intramolecular carbenoid N-H insertion, see: (a) Moyer, M. P, Feldman, P. L, Rapoport, H. J. Org. Chem. 1985, 50. 5223
-
For examples of rhodium-catalyzed intramolecular carbenoid N-H insertion, see: (a) Moyer, M. P.; Feldman, P. L.; Rapoport, H. J. Org. Chem. 1985, 50. 5223.
-
-
-
-
29
-
-
0023133292
-
-
(a) Agami, C.; Platzer. N.; Puchot. C.; Sevestre, H. Tetrahedron 1987, 43, 1091.
-
(1987)
Tetrahedron
, vol.43
, pp. 1091
-
-
Agami, C.1
Platzer, N.2
Puchot, C.3
Sevestre, H.4
-
31
-
-
0030047131
-
-
(c) Mulzer. J.; Meier, A.; Buschmann. J.; Luger, P. J. Org. ('hem. 1996, 61, 566.
-
(1996)
J. Org. ('hem
, vol.61
, pp. 566
-
-
Mulzer, J.1
Meier, A.2
Buschmann, J.3
Luger, P.4
-
32
-
-
0000234509
-
-
Doyle, M. P.; Westerum, L. J.; Wolthuis, N. E.; See, M. M.; Boone. W. P.; Bagheri, V.; Pearson, M. M. J. Am. Chem. Soc. 1993, 115, 958.
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 958
-
-
Doyle, M.P.1
Westerum, L.J.2
Wolthuis, N.E.3
See, M.M.4
Boone, W.P.5
Bagheri, V.6
Pearson, M.M.7
-
33
-
-
0000593386
-
-
Taber, D. F.; You, K. K.; Rheingold, A. L. J. Am. Chem. Soc. 1996, 118, 547.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 547
-
-
Taber, D.F.1
You, K.K.2
Rheingold, A.L.3
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