-
1
-
-
0037366617
-
-
For the general review on Baylis-Hillman reaction, see:
-
For the general review on Baylis-Hillman reaction, see:. Basavaiah D., Rao A.J., and Satyanarayana T. Chem. Rev. 103 (2003) 811-891
-
(2003)
Chem. Rev.
, vol.103
, pp. 811-891
-
-
Basavaiah, D.1
Rao, A.J.2
Satyanarayana, T.3
-
3
-
-
0000892247
-
-
Paquette L.A. (Ed), John Wiley & Sons, New York
-
Ciganek E. In: Paquette L.A. (Ed). Organic Reactions Vol. 51 (1997), John Wiley & Sons, New York 201-350
-
(1997)
Organic Reactions
, vol.51
, pp. 201-350
-
-
Ciganek, E.1
-
12
-
-
4644231912
-
-
For the synthesis of Baylis-Hillman adducts of acrylamides, see:
-
For the synthesis of Baylis-Hillman adducts of acrylamides, see:. Faltin C., Fleming E.M., and Connon S.J. J. Org. Chem. 69 (2004) 6496-6499
-
(2004)
J. Org. Chem.
, vol.69
, pp. 6496-6499
-
-
Faltin, C.1
Fleming, E.M.2
Connon, S.J.3
-
17
-
-
34548425970
-
-
Tang X., Zhang B., He Z., Gao R., and He Z. Adv. Synth. Catal. 349 (2007) 2007-2017
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 2007-2017
-
-
Tang, X.1
Zhang, B.2
He, Z.3
Gao, R.4
He, Z.5
-
20
-
-
18744414203
-
-
Guo W., Wu W., Fan N., Wu Z., and Xia C. Synth. Commun. 35 (2005) 1239-1251
-
(2005)
Synth. Commun.
, vol.35
, pp. 1239-1251
-
-
Guo, W.1
Wu, W.2
Fan, N.3
Wu, Z.4
Xia, C.5
-
22
-
-
0037447912
-
-
Patra A., Batra S., Bhaduri A.P., Khanna A., Chander R., and Dikshit M. Bioorg. Med. Chem. 11 (2003) 2269-2276
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 2269-2276
-
-
Patra, A.1
Batra, S.2
Bhaduri, A.P.3
Khanna, A.4
Chander, R.5
Dikshit, M.6
-
23
-
-
0032338667
-
-
For the formation of non-Baylis-Hillman adducts from acrylamide, see:
-
For the formation of non-Baylis-Hillman adducts from acrylamide, see:. Bussolari J.C., Beers K., Lalan P., Murray W.V., Gauthier D., and McDonnell P. Chem. Lett. (1998) 787-788
-
(1998)
Chem. Lett.
, pp. 787-788
-
-
Bussolari, J.C.1
Beers, K.2
Lalan, P.3
Murray, W.V.4
Gauthier, D.5
McDonnell, P.6
-
24
-
-
0013298724
-
-
For the biotransformation of nitriles to amides, see:
-
For the biotransformation of nitriles to amides, see:. Wang M.-X., and Wu Y. Org. Biomol. Chem. 1 (2003) 535-540
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 535-540
-
-
Wang, M.-X.1
Wu, Y.2
-
25
-
-
36849044127
-
-
Kubac D., Kaplan O., Elisakova V., Patek M., Vejvoda V., Slamova K., Tothova A., Lemaire M., Gallienne E., Lutz-Wahl S., Fischer L., Kuzma M., Pelantova H., van Pelt S., Bolte J., Kren V., and Martinkova L. J. Mol. Catal. B: Enzym. 50 (2008) 107-113
-
(2008)
J. Mol. Catal. B: Enzym.
, vol.50
, pp. 107-113
-
-
Kubac, D.1
Kaplan, O.2
Elisakova, V.3
Patek, M.4
Vejvoda, V.5
Slamova, K.6
Tothova, A.7
Lemaire, M.8
Gallienne, E.9
Lutz-Wahl, S.10
Fischer, L.11
Kuzma, M.12
Pelantova, H.13
van Pelt, S.14
Bolte, J.15
Kren, V.16
Martinkova, L.17
-
26
-
-
33746580710
-
-
For the synthesis and synthetic applications of amide-containing Baylis-Hillman adducts, see:
-
For the synthesis and synthetic applications of amide-containing Baylis-Hillman adducts, see:. Singh V., Yadav G.P., Maulik P.R., and Batra S. Tetrahedron 62 (2006) 8731-8739
-
(2006)
Tetrahedron
, vol.62
, pp. 8731-8739
-
-
Singh, V.1
Yadav, G.P.2
Maulik, P.R.3
Batra, S.4
-
35
-
-
0036589307
-
-
and further references cited therein
-
Kukushkin V.Y., and Pombeiro A.J.L. Chem. Rev. 102 (2002) 1771-1802 and further references cited therein
-
(2002)
Chem. Rev.
, vol.102
, pp. 1771-1802
-
-
Kukushkin, V.Y.1
Pombeiro, A.J.L.2
-
36
-
-
14544273218
-
-
For the hydration of nitriles to amides catalyzed by acid or base, see: and further references cited therein
-
For the hydration of nitriles to amides catalyzed by acid or base, see:. Moorthy J.N., and Singhal N. J. Org. Chem. 70 (2005) 1926-1929 and further references cited therein
-
(2005)
J. Org. Chem.
, vol.70
, pp. 1926-1929
-
-
Moorthy, J.N.1
Singhal, N.2
-
38
-
-
0037047961
-
-
Kopylovich M.N., Kukushkin V.Y., Haukka M., Frausto da Silva J.J.R., and Pombeiro A.J.L. Inorg. Chem. 41 (2002) 4798-4804
-
(2002)
Inorg. Chem.
, vol.41
, pp. 4798-4804
-
-
Kopylovich, M.N.1
Kukushkin, V.Y.2
Haukka, M.3
Frausto da Silva, J.J.R.4
Pombeiro, A.J.L.5
-
44
-
-
44049100990
-
-
For the transition metal-catalyzed hydration of nitriles to amides, see:
-
For the transition metal-catalyzed hydration of nitriles to amides, see:. Goto A., Endo K., and Saito S. Angew. Chem., Int. Ed. 47 (2008) 3607-3609
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 3607-3609
-
-
Goto, A.1
Endo, K.2
Saito, S.3
-
48
-
-
0141534427
-
-
Fung W.K., Huang X., Man M.L., Ng S.M., Hung M.Y., Lin Z., and Lau C.P. J. Am. Chem. Soc. 125 (2003) 11539-11544
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 11539-11544
-
-
Fung, W.K.1
Huang, X.2
Man, M.L.3
Ng, S.M.4
Hung, M.Y.5
Lin, Z.6
Lau, C.P.7
-
49
-
-
30344444437
-
-
Oshiki T., Yamashita H., Sawada K., Utsunomiya M., Takahashi K., and Takai K. Organometallics 24 (2005) 6287-6290
-
(2005)
Organometallics
, vol.24
, pp. 6287-6290
-
-
Oshiki, T.1
Yamashita, H.2
Sawada, K.3
Utsunomiya, M.4
Takahashi, K.5
Takai, K.6
-
52
-
-
0043269708
-
-
Takaya H., Yoshida K., Isozaki K., Terai H., and Murahashi S.-I. Angew. Chem., Int. Ed. 42 (2003) 3302-3304
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 3302-3304
-
-
Takaya, H.1
Yoshida, K.2
Isozaki, K.3
Terai, H.4
Murahashi, S.-I.5
-
57
-
-
70349517819
-
-
note
-
3: C, 65.74; H, 5.98; N, 6.39. Found: C, 65.79; H, 6.07; N, 6.15.
-
-
-
-
58
-
-
70349539596
-
-
note
-
2b described that they failed to prepare compound 2i.
-
-
-
|