-
2
-
-
0000862669
-
-
For reviews of the enantioselective Strecker-type reactions, see:
-
For reviews of the enantioselective Strecker-type reactions, see: Kobayashi S., Ishitani H. Chem. Rev. 99:1999;1069-1094
-
(1999)
Chem. Rev.
, vol.99
, pp. 1069-1094
-
-
Kobayashi, S.1
Ishitani, H.2
-
4
-
-
0034701211
-
-
For more recent reports, see:
-
For more recent reports, see: Porter J.R., Wirschun W.G., Kuntz K.W., Snapper M.L., Hoveyda A.H. J. Am. Chem. Soc. 122:2000;2657-2658
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 2657-2658
-
-
Porter, J.R.1
Wirschun, W.G.2
Kuntz, K.W.3
Snapper, M.L.4
Hoveyda, A.H.5
-
7
-
-
0034810725
-
-
Liu B., Feng X., Chen F., Zhang G., Cui X., Jiang Y. Synlett. 2001;1551-1554
-
(2001)
Synlett
, pp. 1551-1554
-
-
Liu, B.1
Feng, X.2
Chen, F.3
Zhang, G.4
Cui, X.5
Jiang, Y.6
-
11
-
-
0037958740
-
-
Masumoto S., Usuda H., Suzuki M., Kanai M., Shibasaki M. J. Am. Chem. Soc. 125:2003;5634-5635
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5634-5635
-
-
Masumoto, S.1
Usuda, H.2
Suzuki, M.3
Kanai, M.4
Shibasaki, M.5
-
27
-
-
2142776246
-
-
note
-
2AlCN and a chiral ligand was stirred longer, it took much longer time to complete the cyanation
-
-
-
-
30
-
-
0001244096
-
-
Ruano J.L.G., Gamboa A.E., Castro A.M.M., Rodríguez J.H., López-Solera M.I. J. Org. Chem. 63:1998;3324-3332
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3324-3332
-
-
Ruano, J.L.G.1
Gamboa, A.E.2
Castro, A.M.M.3
Rodríguez, J.H.4
López-Solera, M.I.5
-
31
-
-
0035796664
-
-
Ruano J.L.G., García M.C., Laso N.M., Castro A.M.M., Ramos J.H.R. Angew. Chem., Int. Ed. 40:2001;2507-2509
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 2507-2509
-
-
Ruano, J.L.G.1
García, M.C.2
Laso, N.M.3
Castro, A.M.M.4
Ramos, J.H.R.5
-
32
-
-
0037050540
-
-
See also Refs. [4c,e,f,h,j]
-
Ruano J.L.G., García M.C., Castro A.M.M., Ramos J.H.R. Org. Lett. 4:2002;55-57. See also Refs. [4c, e, f, h, j]
-
(2002)
Org. Lett.
, vol.4
, pp. 55-57
-
-
Ruano, J.L.G.1
García, M.C.2
Castro, A.M.M.3
Ramos, J.H.R.4
-
33
-
-
0346122787
-
-
We have recently reported a newly designed chiral ligand having a sulfinyl group:
-
We have recently reported a newly designed chiral ligand having a sulfinyl group: Nakamura S., Fukuzumi T., Toru T. Chirality. 16:2004;10-12
-
(2004)
Chirality
, vol.16
, pp. 10-12
-
-
Nakamura, S.1
Fukuzumi, T.2
Toru, T.3
-
34
-
-
2142850744
-
-
note
-
The absolute stereochemistry of 2a was not determined
-
-
-
-
36
-
-
2142834231
-
-
note
-
2AlCN/ BINOL gave the corresponding cyanated products
-
-
-
-
37
-
-
0033526392
-
-
Krueger C.A., Kuntz K.W., Dzierba C.D., Wirschun W.G., Gleason J.D., Snapper M.L., Hoveyda A.H. J. Am. Chem. Soc. 121:1999;4284-4285
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 4284-4285
-
-
Krueger, C.A.1
Kuntz, K.W.2
Dzierba, C.D.3
Wirschun, W.G.4
Gleason, J.D.5
Snapper, M.L.6
Hoveyda, A.H.7
-
38
-
-
0034595353
-
-
Takamura M., Hamashima Y., Usuda H., Kanai M., Shibasaki M. Angew. Chem., Int. Ed. 39:2000;1650-1652
-
(2000)
Angew. Chem., Int. Ed.
, vol.39
, pp. 1650-1652
-
-
Takamura, M.1
Hamashima, Y.2
Usuda, H.3
Kanai, M.4
Shibasaki, M.5
-
45
-
-
0032575232
-
-
Carbone P., Desimoni G., Faita G., Filippone S., Righetti P. Tetrahedron. 54:1998;6099-6110
-
(1998)
Tetrahedron
, vol.54
, pp. 6099-6110
-
-
Carbone, P.1
Desimoni, G.2
Faita, G.3
Filippone, S.4
Righetti, P.5
-
51
-
-
0031980938
-
-
The dimeric Zr-BINOL complex gives the product having stereochemistry opposite that obtained with the monomeric catalyst:
-
The dimeric Zr-BINOL complex gives the product having stereochemistry opposite that obtained with the monomeric catalyst: Kobayashi S., Komiyama S., Ishitani H. Angew. Chem., Int. Ed. 37:1998;979-981
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 979-981
-
-
Kobayashi, S.1
Komiyama, S.2
Ishitani, H.3
-
53
-
-
2142670222
-
-
note
-
We observed a negative nonlinear effect in the reaction with BINOL, indicating that the aggregation state of the reactive species should be involved
-
-
-
|