-
1
-
-
57649141501
-
-
a values ranging from 18 to 31.5:
-
a values ranging from 18 to 31.5:
-
-
-
-
2
-
-
0029790019
-
-
Maeda H., Fujiwara S., Shin-ike T., Kambe N., and Sonoda N. J. Am. Chem. Soc. 118 (1996) 8160
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 8160
-
-
Maeda, H.1
Fujiwara, S.2
Shin-ike, T.3
Kambe, N.4
Sonoda, N.5
-
3
-
-
0030908521
-
-
Maeda H., Fujiwara S., Nishiyama A., Shin-ike T., Kambe N., and Sonoda N. Synlett (1997) 342
-
(1997)
Synlett
, pp. 342
-
-
Maeda, H.1
Fujiwara, S.2
Nishiyama, A.3
Shin-ike, T.4
Kambe N.5
Sonoda, N.6
-
4
-
-
57649163130
-
-
b:
-
b:
-
-
-
-
5
-
-
1342264104
-
-
Fujiwara S., Nishiyama A., Shin-ike T., Kambe N., and Sonoda N. Org. Lett. 6 (2004) 453
-
(2004)
Org. Lett.
, vol.6
, pp. 453
-
-
Fujiwara, S.1
Nishiyama, A.2
Shin-ike, T.3
Kambe, N.4
Sonoda, N.5
-
6
-
-
27144539526
-
-
Kambe N., Nishiyama A., Fujiwara S., Shin-ike T., and Sonoda N. Phosphorus, Sulfur Silicon Relat. Elem. (2005) 1001
-
(2005)
Phosphorus, Sulfur Silicon Relat. Elem.
, pp. 1001
-
-
Kambe, N.1
Nishiyama, A.2
Fujiwara, S.3
Shin-ike, T.4
Sonoda, N.5
-
7
-
-
33846100053
-
-
N-Carbonylation of lithium azaenolates of amides, formamides, ureas, and carbamates:
-
N-Carbonylation of lithium azaenolates of amides, formamides, ureas, and carbamates:. Fujiwara S., Okada K., Shikano Y., Shimizu Y., Shin-ike T., Terao J., Kambe N., and Sonoda N. J. Org. Chem. 72 (2007) 273
-
(2007)
J. Org. Chem.
, vol.72
, pp. 273
-
-
Fujiwara, S.1
Okada, K.2
Shikano, Y.3
Shimizu, Y.4
Shin-ike, T.5
Terao, J.6
Kambe, N.7
Sonoda, N.8
-
8
-
-
33646447726
-
Thio-, Seleno-, and Telluro-Carboxylic Acid Esters
-
For a recent review on selenol esters:. Kato S. (Ed), Springer, Berlin
-
For a recent review on selenol esters:. Fujiwara S., and Kambe N. Thio-, Seleno-, and Telluro-Carboxylic Acid Esters. In: Kato S. (Ed). Topics in Current Chemistry 251: Chalcogen Carboxylic Acid Derivatives (2005), Springer, Berlin 87-141
-
(2005)
Topics in Current Chemistry 251: Chalcogen Carboxylic Acid Derivatives
, pp. 87-141
-
-
Fujiwara, S.1
Kambe, N.2
-
9
-
-
0034637497
-
-
Imidoylation of lithio derivatives of hydrocarbons:
-
Imidoylation of lithio derivatives of hydrocarbons:. Fujiwara S., Maeda H., Matsuya T., Shin-ike T., Kambe N., and Sonoda N. J. Org. Chem. 65 (2000) 5022
-
(2000)
J. Org. Chem.
, vol.65
, pp. 5022
-
-
Fujiwara, S.1
Maeda, H.2
Matsuya, T.3
Shin-ike, T.4
Kambe, N.5
Sonoda, N.6
-
10
-
-
57649141499
-
-
The reaction of lithium enolates of ketones with Se in the presence of additives such as HMPA followed by trapping with alkyl halides resulted in formation of α-alkylselenoketones. The yields were very low without additives:
-
The reaction of lithium enolates of ketones with Se in the presence of additives such as HMPA followed by trapping with alkyl halides resulted in formation of α-alkylselenoketones. The yields were very low without additives:
-
-
-
-
12
-
-
84986409044
-
-
Swiss K., Choi W.-B., Mohan J., Barum C., Saindane M., Zima G., and Liotta D. Heteroat. Chem. 1 (1990) 141
-
(1990)
Heteroat. Chem.
, vol.1
, pp. 141
-
-
Swiss, K.1
Choi, W.-B.2
Mohan, J.3
Barum, C.4
Saindane, M.5
Zima, G.6
Liotta, D.7
-
14
-
-
0030576892
-
-
We already examined the reaction of isoselenocyanate, having isoelectronic structure with SeCO, with organolithium compounds focusing on the siteselectivities. Phenyllithium attacked selenium exclusively whereas lithium enolate of a ketone reacted with SeCO at both its C- and O-nucleophilic centers attacking the central carbon of SeCO:
-
We already examined the reaction of isoselenocyanate, having isoelectronic structure with SeCO, with organolithium compounds focusing on the siteselectivities. Phenyllithium attacked selenium exclusively whereas lithium enolate of a ketone reacted with SeCO at both its C- and O-nucleophilic centers attacking the central carbon of SeCO:. Maeda H., Kambe N., Sonoda N., Fujiwara S., and Shin-ike T. Tetrahedron 52 (1996) 12165
-
(1996)
Tetrahedron
, vol.52
, pp. 12165
-
-
Maeda, H.1
Kambe, N.2
Sonoda, N.3
Fujiwara, S.4
Shin-ike, T.5
-
15
-
-
0001089561
-
-
For carbophilic addition of organocopper reagents to SeCO:
-
For carbophilic addition of organocopper reagents to SeCO:. Fujiwara S., Asai A., Shin-ike T., Kambe N., and Sonoda N. J. Org. Chem. 63 (1998) 1724
-
(1998)
J. Org. Chem.
, vol.63
, pp. 1724
-
-
Fujiwara, S.1
Asai, A.2
Shin-ike, T.3
Kambe, N.4
Sonoda, N.5
-
23
-
-
11444259910
-
-
McNeil A.J., Toombes G.E.S., Gruner S.M., Lobkovsky E., Collum D.B., Chandramouli S.V., Vanasse B.J., and Ayers T.A. J. Am. Chem. Soc. 126 (2004) 16559
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 16559
-
-
McNeil, A.J.1
Toombes, G.E.S.2
Gruner, S.M.3
Lobkovsky, E.4
Collum, D.B.5
Chandramouli, S.V.6
Vanasse, B.J.7
Ayers, T.A.8
-
28
-
-
41849110273
-
-
Liou L.R., McNeil A.J., Ramirez A., Toombes G.E.S., Gruver J.M., and Collum D.B. J. Am. Chem. Soc. 130 (2008) 4859
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 4859
-
-
Liou, L.R.1
McNeil, A.J.2
Ramirez, A.3
Toombes, G.E.S.4
Gruver, J.M.5
Collum, D.B.6
-
30
-
-
0001093830
-
-
Fraenkel G., Henrichs M., Hewitt J.M., Su B.M., and Geckle M.J. J. Am. Chem. Soc. 102 (1980) 3345
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 3345
-
-
Fraenkel, G.1
Henrichs, M.2
Hewitt, J.M.3
Su, B.M.4
Geckle, M.J.5
-
32
-
-
34247237318
-
-
Pratt L.M., Truhlar D.G., Cramer C.J., Kass S.R., Thompson J.D., and Xidos J.D. J. Org. Chem 72 (2007) 2962
-
(2007)
J. Org. Chem
, vol.72
, pp. 2962
-
-
Pratt, L.M.1
Truhlar, D.G.2
Cramer, C.J.3
Kass, S.R.4
Thompson, J.D.5
Xidos, J.D.6
-
33
-
-
0001330980
-
-
Romesberg F.E., Gilchrist J.H., Harrison A.T., Fuller D.J., and Collum D.B. J. Am. Chem. Soc. 113 (1991) 5751
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 5751
-
-
Romesberg, F.E.1
Gilchrist, J.H.2
Harrison, A.T.3
Fuller, D.J.4
Collum, D.B.5
-
47
-
-
0141704726
-
-
Gaussian, Pittsburgh, PA
-
Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Montgomery Jr. J.A., Vreven T., Kudin K.N., Burant J.C., Millam J.M., Iyengar S.S., Tomasi J., Barone V., Mennucci B., Cossi M., Scalmani G., Rega N., Petersson G.A., Nakatsuji H., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Klene M., Li X., Knox J.E., Hratchian H.P., Cross J.B., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Ayala P.Y., Morokuma K., Voth G.A., Salvador P., Dannenberg J.J., Zakrzewski V.G., Dapprich S., Daniels A.D., Strain M.C., Farkas O., Malick D.K., Rabuck A.D., Raghavachari K., Foresman J.B., Ortiz J.V., Cui Q., Baboul A.G., Clifford S., Cioslowski J., Stefanov B.B., Liu G., Liashenko A., Piskortz P., Komaromi I., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng C.Y., Nanayakkara A., Challacombe M., Gill P.M.W., Johnson B., Chem W., Wong M.W., Gonzalez C., and Pople J.A. Gaussian 03, Revision A.1 (2003), Gaussian, Pittsburgh, PA
-
(2003)
Gaussian 03, Revision A.1
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Montgomery Jr., J.A.7
Vreven, T.8
Kudin, K.N.9
Burant, J.C.10
Millam, J.M.11
Iyengar, S.S.12
Tomasi, J.13
Barone, V.14
Mennucci, B.15
Cossi, M.16
Scalmani, G.17
Rega, N.18
Petersson, G.A.19
Nakatsuji, H.20
Hada, M.21
Ehara, M.22
Toyota, K.23
Fukuda, R.24
Hasegawa, J.25
Ishida, M.26
Nakajima, T.27
Honda, Y.28
Kitao, O.29
Nakai, H.30
Klene, M.31
Li, X.32
Knox, J.E.33
Hratchian, H.P.34
Cross, J.B.35
Adamo, C.36
Jaramillo, J.37
Gomperts, R.38
Stratmann, R.E.39
Yazyev, O.40
Austin, A.J.41
Cammi, R.42
Pomelli, C.43
Ochterski, J.W.44
Ayala, P.Y.45
Morokuma, K.46
Voth, G.A.47
Salvador, P.48
Dannenberg, J.J.49
Zakrzewski, V.G.50
Dapprich, S.51
Daniels, A.D.52
Strain, M.C.53
Farkas, O.54
Malick, D.K.55
Rabuck, A.D.56
Raghavachari, K.57
Foresman, J.B.58
Ortiz, J.V.59
Cui, Q.60
Baboul, A.G.61
Clifford, S.62
Cioslowski, J.63
Stefanov, B.B.64
Liu, G.65
Liashenko, A.66
Piskortz, P.67
Komaromi, I.68
Martin, R.L.69
Fox, D.J.70
Keith, T.71
Al-Laham, M.A.72
Peng, C.Y.73
Nanayakkara, A.74
Challacombe, M.75
Gill, P.M.W.76
Johnson, B.77
Chem, W.78
Wong, M.W.79
Gonzalez, C.80
Pople, J.A.81
more..
-
48
-
-
33749671272
-
-
Pratt L.M., Merry S., Nguyen S.C., Quan P., and Thanh B.T. Tetrahedron 62 (2006) 10821
-
(2006)
Tetrahedron
, vol.62
, pp. 10821
-
-
Pratt, L.M.1
Merry, S.2
Nguyen, S.C.3
Quan, P.4
Thanh, B.T.5
-
51
-
-
33846937053
-
-
Pasumansky L., Collins C.J., Pratt L.M., Nguyen N.V., Ramachandran B., and Singaram B. J. Org. Chem. 72 (2007) 971
-
(2007)
J. Org. Chem.
, vol.72
, pp. 971
-
-
Pasumansky, L.1
Collins, C.J.2
Pratt, L.M.3
Nguyen, N.V.4
Ramachandran, B.5
Singaram, B.6
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