-
1
-
-
33845183545
-
-
Hayashi T., Yamamoto A., Ito Y., Nishioka E., Miura H., Yanagi K. J. Am. Chem. Soc.: 1989; 111 6301
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 6301
-
-
Hayashi, T.1
Yamamoto, A.2
Ito, Y.3
Nishioka, E.4
Miura, H.5
Yanagi, K.6
-
8
-
-
85077842424
-
-
Cheikh R. B., Chaabouni R., Laurent A., Mison P., Nafti A. Synthesis: 1983; 685
-
(1983)
Synthesis
, pp. 685
-
-
Cheikh, R.B.1
Chaabouni, R.2
Laurent, A.3
Mison, P.4
Nafti, A.5
-
14
-
-
68849122846
-
-
Phan T. B., Nolte C., Kobayashi S., Ofial A. R., Mayr H. J. Am. Chem. Soc.: 2009; 131 11392
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 11392
-
-
Phan, T.B.1
Nolte, C.2
Kobayashi, S.3
Ofial, A.R.4
Mayr, H.5
-
17
-
-
34748813040
-
-
Birkholz M.-N, Dubrovina N. V., Shuklov I. A., Holz J., Paciello R., Waloch C., Breit B., Börner A. Tetrahedron: Asymmetry: 2007; 18 2055
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2055
-
-
Birkholz, M.-N.1
Dubrovina, N.V.2
Shuklov, I.A.3
Holz, J.4
Paciello, R.5
Waloch, C.6
Breit, B.7
Börner, A.8
-
18
-
-
4544356395
-
-
Tsarev V. N., Lyubimov S. E., Shiryaev A. A., Zheglov S. V., Bondarev O. G., Davankov V. A., Kabro A. A., Moiseev S. K., Kalinin V. N., Gavrilov K. N. Eur. J. Org. Chem.: 2004; 2214
-
(2004)
Eur. J. Org. Chem.
, pp. 2214
-
-
Tsarev, V.N.1
Lyubimov, S.E.2
Shiryaev, A.A.3
Zheglov, S.V.4
Bondarev, O.G.5
Davankov, V.A.6
Kabro, A.A.7
Moiseev, S.K.8
Kalinin, V.N.9
Gavrilov, K.N.10
-
21
-
-
84906096209
-
-
Gavrilov K. N., Zheglov S. V., Gavrilov V. K., Chuchelkin I. V., Novikov I. M., Shiryaev A. A., Volov A. N., Zamilatskov I. A. Tetrahedron: Asymmetry: 2014; 25 1116
-
(2014)
Tetrahedron: Asymmetry
, vol.25
, pp. 1116
-
-
Gavrilov, K.N.1
Zheglov, S.V.2
Gavrilov, V.K.3
Chuchelkin, I.V.4
Novikov, I.M.5
Shiryaev, A.A.6
Volov, A.N.7
Zamilatskov, I.A.8
-
22
-
-
0034808570
-
-
Deng W.-P, You S.-L, Hou X.-L, Dai L.-X, Yu Y.-H, Xia W., Sun J. J. Am. Chem. Soc.: 2001; 123 6508
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 6508
-
-
Deng, W.-P.1
You, S.-L.2
Hou, X.-L.3
Dai, L.-X.4
Yu, Y.-H.5
Xia, W.6
Sun, J.7
-
23
-
-
0037067541
-
-
You S.-L, Hou X.-L, Dai L.-X, Yu Y.-H, Xia W. J. Org. Chem.: 2002; 67 4684
-
(2002)
J. Org. Chem.
, vol.67
, pp. 4684
-
-
You, S.-L.1
Hou, X.-L.2
Dai, L.-X.3
Yu, Y.-H.4
Xia, W.5
-
24
-
-
0037414501
-
-
Mancheño O. G., Priego J., Cabrera S., Arrayás R. G., Llamas T., Carretero J. C. J. Org. Chem.: 2003; 68 3679
-
(2003)
J. Org. Chem.
, vol.68
, pp. 3679
-
-
Mancheño, O.G.1
Priego, J.2
Cabrera, S.3
Arrayás, R.G.4
Llamas, T.5
Carretero, J.C.6
-
26
-
-
33645856500
-
-
Lam F. L., Au-Yeung T. T. L, Cheung H. Y., Kok S. H. L, Lam W. S., Wong K. Y., Chan A. S. C. Tetrahedron: Asymmetry: 2006; 17 497
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 497
-
-
Lam, F.L.1
Au-Yeung, T.T.L.2
Cheung, H.Y.3
Kok, S.H.L.4
Lam, W.S.5
Wong, K.Y.6
Chan, A.S.C.7
-
31
-
-
35348973992
-
-
Benetsky E. B., Zheglov S. V., Grishina T. B., Macaev F. Z., Bet L. P., Davankov V. A., Gavrilov K. N. Tetrahedron Lett.: 2007; 48 8326
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 8326
-
-
Benetsky, E.B.1
Zheglov, S.V.2
Grishina, T.B.3
Macaev, F.Z.4
Bet, L.P.5
Davankov, V.A.6
Gavrilov, K.N.7
-
32
-
-
76249096185
-
-
Fernández F., Gual A., Claver C., Castillón S., Muller G., Gómez M. Eur. J. Inorg. Chem.: 2010; 758
-
(2010)
Eur. J. Inorg. Chem.
, pp. 758
-
-
Fernández, F.1
Gual, A.2
Claver, C.3
Castillón, S.4
Muller, G.5
Gómez, M.6
-
33
-
-
0033617173
-
-
Evans D. A., Campos K. R., Tedrow J. S., Michael F. E., Gagné M. R. J. Org. Chem.: 1999; 64 2994
-
(1999)
J. Org. Chem.
, vol.64
, pp. 2994
-
-
Evans, D.A.1
Campos, K.R.2
Tedrow, J.S.3
Michael, F.E.4
Gagné, M.R.5
-
34
-
-
0033601268
-
-
Yonehara K., Hashizume T., Mori K., Ohe K., Uemura S. J. Org. Chem.: 1999; 64 9374
-
(1999)
J. Org. Chem.
, vol.64
, pp. 9374
-
-
Yonehara, K.1
Hashizume, T.2
Mori, K.3
Ohe, K.4
Uemura, S.5
-
39
-
-
0042564613
-
-
Nakano H., Yokoyama J., Okuyama Y., Fujita R., Hongo H. Tetrahedron: Asymmetry: 2003; 14 2361
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 2361
-
-
Nakano, H.1
Yokoyama, J.2
Okuyama, Y.3
Fujita, R.4
Hongo, H.5
-
44
-
-
34547223692
-
-
Gavrilov K. N., Lyubimov S. E., Zheglov S. V., Benetsky E. B., Petrovskii P. V., Rastorguev E. A., Grishina T. B., Davankov V. A. Adv. Synth. Catal.: 2007; 349 1085
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 1085
-
-
Gavrilov, K.N.1
Lyubimov, S.E.2
Zheglov, S.V.3
Benetsky, E.B.4
Petrovskii, P.V.5
Rastorguev, E.A.6
Grishina, T.B.7
Davankov, V.A.8
-
45
-
-
36148949667
-
-
Gavrilov K. N., Benetsky E. B., Grishina T. B., Zheglov S. V., Rastorguev E. A., Petrovskii P. V., Macaev F. Z., Davankov V. A. Tetrahedron: Asymmetry: 2007; 18 2557
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2557
-
-
Gavrilov, K.N.1
Benetsky, E.B.2
Grishina, T.B.3
Zheglov, S.V.4
Rastorguev, E.A.5
Petrovskii, P.V.6
Macaev, F.Z.7
Davankov, V.A.8
-
46
-
-
41649092251
-
-
Gavrilov K. N., Zheglov S. V., Vologzhanin P. A., Maksimova M. G., Safronov A. S., Lyubimov S. E., Davankov V. A., Schäffner B., Börner A. Tetrahedron Lett.: 2008; 49 3120
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 3120
-
-
Gavrilov, K.N.1
Zheglov, S.V.2
Vologzhanin, P.A.3
Maksimova, M.G.4
Safronov, A.S.5
Lyubimov, S.E.6
Davankov, V.A.7
Schäffner, B.8
Börner, A.9
-
47
-
-
76949096709
-
-
Lyubimov S. E., Davankov V. A., Gavrilov K. N., Grishina T. B., Rastorguev E. A., Tyutyunov A. A., Verbitskaya T. A., Kalinin V. N., Hey-Hawkins E. Tetrahedron Lett.: 2010; 51 1682
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 1682
-
-
Lyubimov, S.E.1
Davankov, V.A.2
Gavrilov, K.N.3
Grishina, T.B.4
Rastorguev, E.A.5
Tyutyunov, A.A.6
Verbitskaya, T.A.7
Kalinin, V.N.8
Hey-Hawkins, E.9
-
48
-
-
78349253385
-
-
Gavrilov K. N., Zheglov S. V., Rastorguev E. A., Groshkin N. N., Maksimova M. G., Benetsky E. B., Davankov V. A., Reetz M. T. Adv. Synth. Catal.: 2010; 352 2599
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 2599
-
-
Gavrilov, K.N.1
Zheglov, S.V.2
Rastorguev, E.A.3
Groshkin, N.N.4
Maksimova, M.G.5
Benetsky, E.B.6
Davankov, V.A.7
Reetz, M.T.8
-
50
-
-
0035830540
-
-
Nettekoven U., Widhalm M., Kalchhauser H., Kamer P. C. J, van Leeuwen P. W. N. M, Lutz M., Spek A. L. J. Org. Chem.: 2001; 66 759
-
(2001)
J. Org. Chem.
, vol.66
, pp. 759
-
-
Nettekoven, U.1
Widhalm, M.2
Kalchhauser, H.3
Kamer, P.C.J.4
Van Leeuwen, P.W.N.M.5
Lutz, M.6
Spek, A.L.7
-
53
-
-
67650506915
-
-
Popa D., Marcos R., Sayalero S., Vidal-Ferran A., Pericàs M. A. Adv. Synth. Catal.: 2009; 351 1539
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 1539
-
-
Popa, D.1
Marcos, R.2
Sayalero, S.3
Vidal-Ferran, A.4
Pericàs, M.A.5
-
55
-
-
79955391969
-
-
Wang Y., Vaismaa M. J. P, Hämäläinen A. M., Tois J. E., Franzén R. Tetrahedron: Asymmetry: 2011; 22 524
-
(2011)
Tetrahedron: Asymmetry
, vol.22
, pp. 524
-
-
Wang, Y.1
Vaismaa, M.J.P.2
Hämäläinen, A.M.3
Tois, J.E.4
Franzén, R.5
-
56
-
-
0033615761
-
-
Hamada Y., Seto N., Takayanagi Y., Nakano T., Hara O. Tetrahedron Lett.: 1999; 40 7791
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 7791
-
-
Hamada, Y.1
Seto, N.2
Takayanagi, Y.3
Nakano, T.4
Hara, O.5
-
60
-
-
84904967917
-
-
Feng B., Cheng H.-G, Chen J.-R, Deng Q.-H, Lu L.-Q, Xiao W.-J. Chem. Commun.: 2014; 50 9550
-
(2014)
Chem. Commun.
, vol.50
, pp. 9550
-
-
Feng, B.1
Cheng, H.-G.2
Chen, J.-R.3
Deng, Q.-H.4
Lu, L.-Q.5
Xiao, W.-J.6
-
61
-
-
0036977771
-
-
Priego J., Mancheño O. G., Cabrera S., Arrayás R. G., Llamas T., Carretero J. C. Chem. Commun.: 2002; 2512
-
(2002)
Chem. Commun.
, pp. 2512
-
-
Priego, J.1
Mancheño, O.G.2
Cabrera, S.3
Arrayás, R.G.4
Llamas, T.5
Carretero, J.C.6
-
64
-
-
84925822033
-
-
Wu H., Xie F., Wang Y., Zhao X., Liu D., Zhang W. Org. Biomol. Chem.: 2015; 13 4248
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 4248
-
-
Wu, H.1
Xie, F.2
Wang, Y.3
Zhao, X.4
Liu, D.5
Zhang, W.6
-
66
-
-
1842637842
-
-
Takacs J. M., Reddy D. S., Moteki S. A., Wu D., Palencia H. J. Am. Chem. Soc.: 2004; 126 4494
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 4494
-
-
Takacs, J.M.1
Reddy, D.S.2
Moteki, S.A.3
Wu, D.4
Palencia, H.5
-
67
-
-
26444603763
-
-
Nemoto T., Masuda T., Akimoto Y., Fukuyama T., Hamada Y. Org. Lett.: 2005; 7 4447
-
(2005)
Org. Lett.
, vol.7
, pp. 4447
-
-
Nemoto, T.1
Masuda, T.2
Akimoto, Y.3
Fukuyama, T.4
Hamada, Y.5
-
70
-
-
67849128913
-
-
Trost B. M., Malhotra S., Olson D. E., Maruniak A., Du Bois J. J. Am. Chem. Soc.: 2009; 131 4190
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 4190
-
-
Trost, B.M.1
Malhotra, S.2
Olson, D.E.3
Maruniak, A.4
Du Bois, J.5
-
71
-
-
0142196051
-
-
For enantioconvergent allylic amination of an aliphatic electrophile in unspecified yield with a pre-formed palladium/bisoxazolylphosphine complex, see: Yamagishi T., Ohnuki M., Kiyooka T., Masui D., Sato K., Yamaguchi M. Tetrahedron: Asymmetry: 2003; 14 3275
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 3275
-
-
Yamagishi, T.1
Ohnuki, M.2
Kiyooka, T.3
Masui, D.4
Sato, K.5
Yamaguchi, M.6
-
72
-
-
0037255763
-
-
Humphries M. E., Clark B. P., Regini S., Acemoglu L., Williams J. M. J. Chirality: 2003; 15 190
-
(2003)
Chirality
, vol.15
, pp. 190
-
-
Humphries, M.E.1
Clark, B.P.2
Regini, S.3
Acemoglu, L.4
Williams, J.M.J.5
-
78
-
-
0033938654
-
-
Bremberg U., Lutsenko S., Kaiser N.-F, Larhed M., Hallberg A., Moberg C. Synthesis: 2000; 1004
-
(2000)
Synthesis
, pp. 1004
-
-
Bremberg, U.1
Lutsenko, S.2
Kaiser, N.-F.3
Larhed, M.4
Hallberg, A.5
Moberg, C.6
-
79
-
-
45549100945
-
-
For the reaction of TMS-phthalimide with a bicyclic allylic lactone, see: Trost B. M., Zhang T. Angew. Chem. Int. Ed.: 2008; 47 3759
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 3759
-
-
Trost, B.M.1
Zhang, T.2
-
83
-
-
84938999765
-
-
Nemoto T., Yamaguchi M., Kakugawa K., Harada S., Hamada Y. Adv. Synth. Catal.: 2015; 357 2547
-
(2015)
Adv. Synth. Catal.
, vol.357
, pp. 2547
-
-
Nemoto, T.1
Yamaguchi, M.2
Kakugawa, K.3
Harada, S.4
Hamada, Y.5
-
84
-
-
0035847526
-
-
The monodentate phosphine ligand (-)-9-PBN (19), which was one of the leading ligands for the benchmark acyclic system (Table 1) also performs well with an aryl-substituted cyclohexenol derivative, see: Hamada Y., Sakaguchi K., Hatano K., Hara O. Tetrahedron Lett.: 2001; 42 1297
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 1297
-
-
Hamada, Y.1
Sakaguchi, K.2
Hatano, K.3
Hara, O.4
-
85
-
-
84950110034
-
-
A diamidophosphite ligand is also effective with both cyclic and acyclic substrates, see: Gavrilov K. N., Zheglov S. V., Gavrilov V. K., Maksimova M. G., Zamilatskov I. A. Russ. Chem. Bull.: 2015; 64 967
-
(2015)
Russ. Chem. Bull.
, vol.64
, pp. 967
-
-
Gavrilov, K.N.1
Zheglov, S.V.2
Gavrilov, V.K.3
Maksimova, M.G.4
Zamilatskov, I.A.5
-
86
-
-
84899826405
-
-
Kawatsura M., Terasaki S., Minakawa M., Hirakawa T., Ikeda K., Itoh T. Org. Lett.: 2014; 16 2442
-
(2014)
Org. Lett.
, vol.16
, pp. 2442
-
-
Kawatsura, M.1
Terasaki, S.2
Minakawa, M.3
Hirakawa, T.4
Ikeda, K.5
Itoh, T.6
-
87
-
-
84885461207
-
-
Quan M., Butt N., Shen J., Shen K., Liu D., Zhang W. Org. Biomol. Chem.: 2013; 11 7412
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 7412
-
-
Quan, M.1
Butt, N.2
Shen, J.3
Shen, K.4
Liu, D.5
Zhang, W.6
-
92
-
-
0034823238
-
-
You S.-L, Zhu X.-Z, Luo Y.-M, Hou X.-L, Dai L.-X. J. Am. Chem. Soc.: 2001; 123 7471
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 7471
-
-
You, S.-L.1
Zhu, X.-Z.2
Luo, Y.-M.3
Hou, X.-L.4
Dai, L.-X.5
-
94
-
-
84865838724
-
-
Wang X., Meng F., Wang Y., Han Z., Chen Y.-J, Liu L., Wang Z., Ding K. Angew. Chem. Int. Ed.: 2012; 51 9276
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 9276
-
-
Wang, X.1
Meng, F.2
Wang, Y.3
Han, Z.4
Chen, Y.-J.5
Liu, L.6
Wang, Z.7
Ding, K.8
-
95
-
-
84892151261
-
-
Wang X., Guo P., Han Z., Wang X., Wang Z., Ding K. J. Am. Chem. Soc.: 2014; 136 405
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 405
-
-
Wang, X.1
Guo, P.2
Han, Z.3
Wang, X.4
Wang, Z.5
Ding, K.6
-
98
-
-
27644536211
-
-
Alibés R., Bayón P., de March P., Figueredo M., Font J., García-García E., González-Gálvez D. Org. Lett.: 2005; 7 5107
-
(2005)
Org. Lett.
, vol.7
, pp. 5107
-
-
Alibés, R.1
Bayón, P.2
De March, P.3
Figueredo, M.4
Font, J.5
García-García, E.6
González-Gálvez, D.7
-
99
-
-
70349099593
-
-
González-Gálvez D., García-García E., Alibés R., Bayón P., de March P., Figueredo M., Font J. J. Org. Chem.: 2009; 74 6199
-
(2009)
J. Org. Chem.
, vol.74
, pp. 6199
-
-
González-Gálvez, D.1
García-García, E.2
Alibés, R.3
Bayón, P.4
De March, P.5
Figueredo, M.6
Font, J.7
-
101
-
-
68149084782
-
-
Mangion I., Strotman N., Drahl M., Imbriglio J., Guidry E. Org. Lett.: 2009; 11 3258
-
(2009)
Org. Lett.
, vol.11
, pp. 3258
-
-
Mangion, I.1
Strotman, N.2
Drahl, M.3
Imbriglio, J.4
Guidry, E.5
-
106
-
-
84920381611
-
-
Vinylethylene carbonates can be used in place of aziridines and provide 4-vinyloxazolidinones in high yields and enantiomeric excess, see: Khan A., Xing J., Zhao J., Kan Y., Zhang W., Zhang Y. J. Chem. Eur. J.: 2015; 21 120
-
(2015)
Chem. Eur. J.
, vol.21
, pp. 120
-
-
Khan, A.1
Xing, J.2
Zhao, J.3
Kan, Y.4
Zhang, W.5
Zhang, Y.J.6
-
119
-
-
84896766643
-
-
Kawatsura M., Uchida K., Terasaki S., Tsuji H., Minakawa M., Itoh T. Org. Lett.: 2014; 16 1470
-
(2014)
Org. Lett.
, vol.16
, pp. 1470
-
-
Kawatsura, M.1
Uchida, K.2
Terasaki, S.3
Tsuji, H.4
Minakawa, M.5
Itoh, T.6
-
120
-
-
33846933027
-
-
Helmchen G., Dahnz A., Dübon P., Schelwies M., Weihofen R. Chem. Commun.: 2007; 675
-
(2007)
Chem. Commun.
, pp. 675
-
-
Helmchen, G.1
Dahnz, A.2
Dübon, P.3
Schelwies, M.4
Weihofen, R.5
-
122
-
-
0035802358
-
-
Takeuchi R., Ue N., Tanabe K., Yamashita K., Shiga N. J. Am. Chem. Soc.: 2001; 123 9525
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 9525
-
-
Takeuchi, R.1
Ue, N.2
Tanabe, K.3
Yamashita, K.4
Shiga, N.5
-
123
-
-
84948667415
-
-
Weak, attractive non-covalent interactions involving a vinylic C-H bond of the COD ligand may be responsible for high branched regioselectivities observed in iridium-catalyzed allylic substitution reactions, see: Madrahimov S. T., Li Q., Sharma A., Hartwig J. F. J. Am. Chem. Soc.: 2015; 137 14968
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 14968
-
-
Madrahimov, S.T.1
Li, Q.2
Sharma, A.3
Hartwig, J.F.4
-
126
-
-
33646183971
-
-
Polet D., Alexakis A., Tissot-Croset K., Corminboeuf C., Ditrich K. Chem. Eur. J.: 2006; 12 3596
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 3596
-
-
Polet, D.1
Alexakis, A.2
Tissot-Croset, K.3
Corminboeuf, C.4
Ditrich, K.5
-
127
-
-
54749126182
-
-
Spiess S., Welter C., Franck G., Taquet J.-P, Helmchen G. Angew. Chem. Int. Ed.: 2008; 47 7652
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7652
-
-
Spiess, S.1
Welter, C.2
Franck, G.3
Taquet, J.-P.4
Helmchen, G.5
-
128
-
-
84880921332
-
-
Ye K.-Y, Zhao Z.-A, Lai Z.-W, Dai L.-X, You S.-L. Synthesis: 2013; 45 2109
-
(2013)
Synthesis
, vol.45
, pp. 2109
-
-
Ye, K.-Y.1
Zhao, Z.-A.2
Lai, Z.-W.3
Dai, L.-X.4
You, S.-L.5
-
132
-
-
79960319418
-
-
Krausová Z., Sehnal P., Bondzic B. P., Chercheja S., Eilbracht P., Stará I. G., Šaman D., Starý I. Eur. J. Org. Chem.: 2011; 3849
-
(2011)
Eur. J. Org. Chem.
, pp. 3849
-
-
Krausová, Z.1
Sehnal, P.2
Bondzic, B.P.3
Chercheja, S.4
Eilbracht, P.5
Stará, I.G.6
Šaman, D.7
Starý, I.8
-
133
-
-
84885950454
-
-
Hoecker J., Rudolf G. C., Bächle F., Fleischer S., Lindner B. D., Helmchen G. Eur. J. Org. Chem.: 2013; 5149
-
(2013)
Eur. J. Org. Chem.
, pp. 5149
-
-
Hoecker, J.1
Rudolf, G.C.2
Bächle, F.3
Fleischer, S.4
Lindner, B.D.5
Helmchen, G.6
-
135
-
-
55349144524
-
-
Gnamm C., Franck G., Miller N., Stork T., Brödner K., Helmchen G. Synthesis: 2008; 3331
-
(2008)
Synthesis
, pp. 3331
-
-
Gnamm, C.1
Franck, G.2
Miller, N.3
Stork, T.4
Brödner, K.5
Helmchen, G.6
-
139
-
-
84868020743
-
-
Raskatov J. A., Jäkel M., Straub B. F., Rominger F., Helmchen G. Chem. Eur. J.: 2012; 18 14314
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 14314
-
-
Raskatov, J.A.1
Jäkel, M.2
Straub, B.F.3
Rominger, F.4
Helmchen, G.5
-
150
-
-
79951827490
-
-
Farwick A., Engelhart J. U., Tverskoy O., Welter C., Umlauf Q. A., Rominger F., Kerr W. J., Helmchen G. Adv. Synth. Catal.: 2011; 353 349
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 349
-
-
Farwick, A.1
Engelhart, J.U.2
Tverskoy, O.3
Welter, C.4
Umlauf, Q.A.5
Rominger, F.6
Kerr, W.J.7
Helmchen, G.8
-
160
-
-
84957848826
-
-
2 improves the regio- and enantioseletivity slightly, see
-
2 improves the regio- and enantioseletivity slightly, see: Seehafer K., Malakar C. C., Bender M., Qu J., Liang C., Helmchen G. Eur. J. Org. Chem.: 2016; 493
-
(2016)
Eur. J. Org. Chem.
, pp. 493
-
-
Seehafer, K.1
Malakar, C.C.2
Bender, M.3
Qu, J.4
Liang, C.5
Helmchen, G.6
-
161
-
-
35048813934
-
-
Pouy M. J., Leitner A., Weix D. J., Ueno S., Hartwig J. F. Org. Lett.: 2007; 9 3949
-
(2007)
Org. Lett.
, vol.9
, pp. 3949
-
-
Pouy, M.J.1
Leitner, A.2
Weix, D.J.3
Ueno, S.4
Hartwig, J.F.5
-
163
-
-
79957823107
-
-
Gärtner M., Jäkel M., Achatz M., Sonnenschein C., Tverskoy O., Helmchen G. Org. Lett.: 2011; 13 2810
-
(2011)
Org. Lett.
, vol.13
, pp. 2810
-
-
Gärtner, M.1
Jäkel, M.2
Achatz, M.3
Sonnenschein, C.4
Tverskoy, O.5
Helmchen, G.6
-
169
-
-
78650372218
-
-
Tosatti P., Horn J., Campbell A. J., House D., Nelson A., Marsden S. P. Adv. Synth. Catal.: 2010; 352 3153
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 3153
-
-
Tosatti, P.1
Horn, J.2
Campbell, A.J.3
House, D.4
Nelson, A.5
Marsden, S.P.6
-
170
-
-
79959637674
-
-
Tosatti P., Campbell A. J., House D., Nelson A., Marsden S. P. J. Org. Chem.: 2011; 76 5495
-
(2011)
J. Org. Chem.
, vol.76
, pp. 5495
-
-
Tosatti, P.1
Campbell, A.J.2
House, D.3
Nelson, A.4
Marsden, S.P.5
-
172
-
-
84873337147
-
-
Lee J. S., Kim D., Lozano L., Kong S. B., Han H. Org. Lett.: 2013; 15 554
-
(2013)
Org. Lett.
, vol.15
, pp. 554
-
-
Lee, J.S.1
Kim, D.2
Lozano, L.3
Kong, S.B.4
Han, H.5
-
173
-
-
17444425377
-
-
Welter C., Dahnz A., Brunner B., Streiff S., Dübon P., Helmchen G. Org. Lett.: 2005; 7 1239
-
(2005)
Org. Lett.
, vol.7
, pp. 1239
-
-
Welter, C.1
Dahnz, A.2
Brunner, B.3
Streiff, S.4
Dübon, P.5
Helmchen, G.6
-
180
-
-
84894790843
-
-
Natori Y., Kikuchi S., Kondo T., Saito Y., Yoshimura Y., Takahata H. Org. Biomol. Chem.: 2014; 12 1983
-
(2014)
Org. Biomol. Chem.
, vol.12
, pp. 1983
-
-
Natori, Y.1
Kikuchi, S.2
Kondo, T.3
Saito, Y.4
Yoshimura, Y.5
Takahata, H.6
-
187
-
-
83055165927
-
-
Ye K.-Y, He H., Liu W.-B, Dai L.-X, Helmchen G., You S.-L. J. Am. Chem. Soc.: 2011; 133 19006
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 19006
-
-
Ye, K.-Y.1
He, H.2
Liu, W.-B.3
Dai, L.-X.4
Helmchen, G.5
You, S.-L.6
-
190
-
-
84948744483
-
-
For an example of azetidine formation via palladium-catalyzed intramolecular allylic substitution with modest diastereocontrol, see
-
For an example of azetidine formation via palladium-catalyzed intramolecular allylic substitution with modest diastereocontrol, see: Wei X., Liu D., An Q., Zhang W. Org. Lett.: 2015; 17 5768
-
(2015)
Org. Lett.
, vol.17
, pp. 5768
-
-
Wei, X.1
Liu, D.2
An, Q.3
Zhang, W.4
-
207
-
-
0037130740
-
-
Ozawa F., Okamoto H., Kawagishi S., Yamamoto S., Minami T., Yoshifuji M. J. Am. Chem. Soc.: 2002; 124 10968
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 10968
-
-
Ozawa, F.1
Okamoto, H.2
Kawagishi, S.3
Yamamoto, S.4
Minami, T.5
Yoshifuji, M.6
-
208
-
-
78650179391
-
-
Hirakawa T., Ikeda K., Ogasa H., Kawatsura M., Itoh T. Synlett: 2010; 2887
-
(2010)
Synlett
, pp. 2887
-
-
Hirakawa, T.1
Ikeda, K.2
Ogasa, H.3
Kawatsura, M.4
Itoh, T.5
-
210
-
-
77954348359
-
-
Cardillo G., Gentilucci L., Mosconi E., Tolomelli A., Troisi S., Juaristi E. Tetrahedron: 2010; 66 4994
-
(2010)
Tetrahedron
, vol.66
, pp. 4994
-
-
Cardillo, G.1
Gentilucci, L.2
Mosconi, E.3
Tolomelli, A.4
Troisi, S.5
Juaristi, E.6
-
212
-
-
10344224590
-
-
Shing T. K. M, Kwong C. S. K, Cheung A. W. C, Kok S. H.-L, Yu Z., Li J., Cheng C. H. K. J. Am. Chem. Soc.: 2004; 126 15990
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15990
-
-
Shing, T.K.M.1
Kwong, C.S.K.2
Cheung, A.W.C.3
Kok, S.H.-L.4
Yu, Z.5
Li, J.6
Cheng, C.H.K.7
-
213
-
-
79960228405
-
-
For another example of a diastereospecific palladium-catalyzed allylic substitution involving carbohydrates, see
-
For another example of a diastereospecific palladium-catalyzed allylic substitution involving carbohydrates, see: Cumpstey I., Ramstadius C., Borbas K. E. Synlett: 2011; 1701
-
(2011)
Synlett
, pp. 1701
-
-
Cumpstey, I.1
Ramstadius, C.2
Borbas, K.E.3
-
214
-
-
0037009728
-
-
Verhelst S. H. L, Wiedenhof W., Ovaa H., van der Marel G. A., Overkleeft H. S., van Boeckel C. A. A, van Boom J. H. Tetrahedron Lett.: 2002; 43 6451
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 6451
-
-
Verhelst, S.H.L.1
Wiedenhof, W.2
Ovaa, H.3
Van Der Marel, G.A.4
Overkleeft, H.S.5
Van Boeckel, C.A.A.6
Van Boom, J.H.7
-
219
-
-
84943240426
-
-
Zhang M., Watanabe K., Tsukamoto M., Shibuya R., Morimoto H., Ohshima T. Chem. Eur. J.: 2015; 21 3937
-
(2015)
Chem. Eur. J.
, vol.21
, pp. 3937
-
-
Zhang, M.1
Watanabe, K.2
Tsukamoto, M.3
Shibuya, R.4
Morimoto, H.5
Ohshima, T.6
-
225
-
-
84862734174
-
-
Zhao M.-X, Chen M.-X, Tang W.-H, Wei D.-K, Dai T.-L, Shi M. Eur. J. Org. Chem.: 2012; 3598
-
(2012)
Eur. J. Org. Chem.
, pp. 3598
-
-
Zhao, M.-X.1
Chen, M.-X.2
Tang, W.-H.3
Wei, D.-K.4
Dai, T.-L.5
Shi, M.6
-
227
-
-
84957842205
-
-
A cyclohexane-based thiourea-phosphine organocatalyst is also effective in the enantioconvergent allylic amination reaction involving phthalimide as the pronucleophile, see
-
A cyclohexane-based thiourea-phosphine organocatalyst is also effective in the enantioconvergent allylic amination reaction involving phthalimide as the pronucleophile, see: Zhao X., Kang T., Shen J., Sha F., Wu X. Chin. J. Chem.: 2015; 33 1333
-
(2015)
Chin. J. Chem.
, vol.33
, pp. 1333
-
-
Zhao, X.1
Kang, T.2
Shen, J.3
Sha, F.4
Wu, X.5
-
229
-
-
84865242015
-
-
Zhang H., Zhang S.-J, Zhou Q.-Q, Dong L., Chen Y.-C. Beilstein J. Org. Chem.: 2012; 8 1241
-
(2012)
Beilstein J. Org. Chem.
, vol.8
, pp. 1241
-
-
Zhang, H.1
Zhang, S.-J.2
Zhou, Q.-Q.3
Dong, L.4
Chen, Y.-C.5
-
235
-
-
77957197373
-
-
Yamamoto H., Ho E., Namba K., Imagawa H., Nishizawa M. Chem. Eur. J.: 2010; 16 11271
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 11271
-
-
Yamamoto, H.1
Ho, E.2
Namba, K.3
Imagawa, H.4
Nishizawa, M.5
-
240
-
-
48849103939
-
-
Benfatti F., Cardillo G., Gentilucci L., Mosconi E., Tolomelli A. Org. Lett.: 2008; 10 2425
-
(2008)
Org. Lett.
, vol.10
, pp. 2425
-
-
Benfatti, F.1
Cardillo, G.2
Gentilucci, L.3
Mosconi, E.4
Tolomelli, A.5
-
241
-
-
70749119425
-
-
Cardillo G., Gennari A., Gentilucci L., Mosconi E., Tolomelli A., Troisi S. Eur. J. Org. Chem.: 2009; 5991
-
(2009)
Eur. J. Org. Chem.
, pp. 5991
-
-
Cardillo, G.1
Gennari, A.2
Gentilucci, L.3
Mosconi, E.4
Tolomelli, A.5
Troisi, S.6
-
242
-
-
84879886502
-
-
Li Q. R., Dong G. R., Park S. J., Hong Y. R., Kim I. S., Jung Y. H. Eur. J. Org. Chem.: 2013; 4427
-
(2013)
Eur. J. Org. Chem.
, pp. 4427
-
-
Li, Q.R.1
Dong, G.R.2
Park, S.J.3
Hong, Y.R.4
Kim, I.S.5
Jung, Y.H.6
-
244
-
-
84887049307
-
-
Li Q. R., Kim S. I., Park S. J., Yang H. R., Baek A. R., Kim I. S., Jung Y. H. Tetrahedron: 2013; 69 10384
-
(2013)
Tetrahedron
, vol.69
, pp. 10384
-
-
Li, Q.R.1
Kim, S.I.2
Park, S.J.3
Yang, H.R.4
Baek, A.R.5
Kim, I.S.6
Jung, Y.H.7
-
245
-
-
84055200153
-
-
Lee S. H., Kim I. S., Li Q. R., Dong G. R., Jeong L. S., Jung Y. H. J. Org. Chem.: 2011; 76 10011
-
(2011)
J. Org. Chem.
, vol.76
, pp. 10011
-
-
Lee, S.H.1
Kim, I.S.2
Li, Q.R.3
Dong, G.R.4
Jeong, L.S.5
Jung, Y.H.6
-
247
-
-
84959545685
-
-
Timoshenko M. A., Kharitonov Y. V., Shakirov M. M., Bagryanskaya I., Shults E. E. ChemistryOpen: 2016; 5 65
-
(2016)
ChemistryOpen
, vol.5
, pp. 65
-
-
Timoshenko, M.A.1
Kharitonov, Y.V.2
Shakirov, M.M.3
Bagryanskaya, I.4
Shults, E.E.5
-
249
-
-
84933525336
-
-
Kuroda Y., Harada S., Oonishi A., Yamaoka Y., Yamada K., Takasu K. Angew. Chem. Int. Ed.: 2015; 54 8263
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 8263
-
-
Kuroda, Y.1
Harada, S.2
Oonishi, A.3
Yamaoka, Y.4
Yamada, K.5
Takasu, K.6
-
254
-
-
79956115470
-
-
Ichikawa Y., Matsuda Y., Okumura K., Nakamura M., Masuda T., Kotsuki H., Nakano K. Org. Lett.: 2011; 13 2520
-
(2011)
Org. Lett.
, vol.13
, pp. 2520
-
-
Ichikawa, Y.1
Matsuda, Y.2
Okumura, K.3
Nakamura, M.4
Masuda, T.5
Kotsuki, H.6
Nakano, K.7
-
256
-
-
0001923963
-
-
For another example of a diastereospecific [3,3]-sigmatropic rearrangement involving an allylic trifluoroacetimidate, see
-
For another example of a diastereospecific [3,3]-sigmatropic rearrangement involving an allylic trifluoroacetimidate, see: Savage I., Thomas E. J., Wilson P. D. J. Chem. Soc., Perkin Trans. 1: 1999; 3291
-
(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 3291
-
-
Savage, I.1
Thomas, E.J.2
Wilson, P.D.3
-
260
-
-
79953221519
-
-
Xu C., Liu Z., Wang H., Zhang B., Xiang Z., Hao X., Wang D. Z. Org. Lett.: 2011; 13 1812
-
(2011)
Org. Lett.
, vol.13
, pp. 1812
-
-
Xu, C.1
Liu, Z.2
Wang, H.3
Zhang, B.4
Xiang, Z.5
Hao, X.6
Wang, D.Z.7
-
261
-
-
84975780867
-
-
Amann F., Frank M., Rhodes R., Robinson A., Kesselgruber M., Abele S. Org. Process Res. Dev.: 2016; 20 446
-
(2016)
Org. Process Res. Dev.
, vol.20
, pp. 446
-
-
Amann, F.1
Frank, M.2
Rhodes, R.3
Robinson, A.4
Kesselgruber, M.5
Abele, S.6
-
262
-
-
84864215190
-
-
Kitamoto K., Nakayama Y., Sampei M., Ichiki M., Furuya N., Sato T., Chida N. Eur. J. Org. Chem.: 2012; 4217
-
(2012)
Eur. J. Org. Chem.
, pp. 4217
-
-
Kitamoto, K.1
Nakayama, Y.2
Sampei, M.3
Ichiki, M.4
Furuya, N.5
Sato, T.6
Chida, N.7
-
263
-
-
84926443884
-
-
Tsuzaki S., Usui S., Oishi H., Yasushima D., Fukuyasu T., Oishi T., Sato T., Chida N. Org. Lett.: 2015; 17 1704
-
(2015)
Org. Lett.
, vol.17
, pp. 1704
-
-
Tsuzaki, S.1
Usui, S.2
Oishi, H.3
Yasushima, D.4
Fukuyasu, T.5
Oishi, T.6
Sato, T.7
Chida, N.8
-
267
-
-
54549096756
-
-
Ichikawa Y., Matsunaga K., Masuda T., Kotsuki H., Nakano K. Tetrahedron: 2008; 64 11313
-
(2008)
Tetrahedron
, vol.64
, pp. 11313
-
-
Ichikawa, Y.1
Matsunaga, K.2
Masuda, T.3
Kotsuki, H.4
Nakano, K.5
-
273
-
-
84858172940
-
-
Molander G.A. Evans P.A. Georg Thieme Stuttgart
-
Jautze S., Peters R. In Science of Synthesis. Vol 3 Molander G. A., Evans P. A. Georg Thieme Stuttgart: 2011; 443
-
(2011)
In Science of Synthesis
, vol.3
, pp. 443
-
-
Jautze, S.1
Peters, R.2
-
280
-
-
69749094244
-
-
Fischer D. F., Barakat A., Xin Z.-q, Weiss M. E., Peters R. Chem. Eur. J.: 2009; 15 8722
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 8722
-
-
Fischer, D.F.1
Barakat, A.2
Xin, Z.-Q.3
Weiss, M.E.4
Peters, R.5
-
281
-
-
84902201203
-
-
Hellmuth T., Rieckhoff S., Weiss M., Dorst K., Frey W., Peters R. ACS Catal.: 2014; 4 1850
-
(2014)
ACS Catal.
, vol.4
, pp. 1850
-
-
Hellmuth, T.1
Rieckhoff, S.2
Weiss, M.3
Dorst, K.4
Frey, W.5
Peters, R.6
-
283
-
-
33748551071
-
-
Weiss M. E., Fischer D. F., Xin Z.-q, Jautze S., Schweizer W. B., Peters R. Angew. Chem. Int. Ed.: 2006; 45 5694
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5694
-
-
Weiss, M.E.1
Fischer, D.F.2
Xin, Z.-Q.3
Jautze, S.4
Schweizer, W.B.5
Peters, R.6
-
285
-
-
84866059086
-
-
A mixed pallada-/platinacycle is also effective at 0.05 mol% loadings, see
-
A mixed pallada-/platinacycle is also effective at 0.05 mol% loadings, see: Weiss M., Frey W., Peters R. Organometallics: 2012; 31 6365
-
(2012)
Organometallics
, vol.31
, pp. 6365
-
-
Weiss, M.1
Frey, W.2
Peters, R.3
-
286
-
-
84858193860
-
-
Eitel S. H., Bauer M., Schweinfurth D., Deibel N., Sarkar B., Kelm H., Krüger H.-J, Frey W., Peters R. J. Am. Chem. Soc.: 2012; 134 4683
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 4683
-
-
Eitel, S.H.1
Bauer, M.2
Schweinfurth, D.3
Deibel, N.4
Sarkar, B.5
Kelm, H.6
Krüger, H.-J.7
Frey, W.8
Peters, R.9
-
297
-
-
84948845064
-
-
West T. H., Spoehrle S. M., Kasten K., Taylor J. E., Smith A. D. ACS Catal.: 2015; 5 7446
-
(2015)
ACS Catal.
, vol.5
, pp. 7446
-
-
West, T.H.1
Spoehrle, S.M.2
Kasten, K.3
Taylor, J.E.4
Smith, A.D.5
-
298
-
-
0001215094
-
-
Shea R. G., Fitzner J. N., Fankhauser J. E., Spaltenstein A., Carpino P. A., Peevey R. M., Pratt D. V., Tenge B. J., Hopkins P. B. J. Org. Chem.: 1986; 51 5243
-
(1986)
J. Org. Chem.
, vol.51
, pp. 5243
-
-
Shea, R.G.1
Fitzner, J.N.2
Fankhauser, J.E.3
Spaltenstein, A.4
Carpino, P.A.5
Peevey, R.M.6
Pratt, D.V.7
Tenge, B.J.8
Hopkins, P.B.9
-
300
-
-
33646507896
-
-
Armstrong A., Challinor L., Cooke R. S., Moir J. H., Treweeke N. R. J. Org. Chem.: 2006; 71 4028
-
(2006)
J. Org. Chem.
, vol.71
, pp. 4028
-
-
Armstrong, A.1
Challinor, L.2
Cooke, R.S.3
Moir, J.H.4
Treweeke, N.R.5
-
303
-
-
0034794585
-
-
Ishikawa T., Kawakami M., Fukui M., Yamashita A., Urano J., Saito S. J. Am. Chem. Soc.: 2001; 123 7734
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 7734
-
-
Ishikawa, T.1
Kawakami, M.2
Fukui, M.3
Yamashita, A.4
Urano, J.5
Saito, S.6
-
306
-
-
0033575405
-
-
Honda T., Koizumi T., Komatsuzaki Y., Yamashita R., Kanai K., Nagase H. Tetrahedron: Asymmetry: 1999; 10 2703
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 2703
-
-
Honda, T.1
Koizumi, T.2
Komatsuzaki, Y.3
Yamashita, R.4
Kanai, K.5
Nagase, H.6
-
308
-
-
53549095407
-
-
Müller T. E., Hultzsch K. C., Yus M., Foubelo F., Tada M. Chem. Rev.: 2008; 108 3795
-
(2008)
Chem. Rev.
, vol.108
, pp. 3795
-
-
Müller, T.E.1
Hultzsch, K.C.2
Yus, M.3
Foubelo, F.4
Tada, M.5
-
318
-
-
80054895613
-
-
Liu W., Zhang D., Zheng S., Yue Y., Liu D., Zhao X. Eur. J. Org. Chem.: 2011; 6288
-
(2011)
Eur. J. Org. Chem.
, pp. 6288
-
-
Liu, W.1
Zhang, D.2
Zheng, S.3
Yue, Y.4
Liu, D.5
Zhao, X.6
-
322
-
-
79951482180
-
-
Shapiro N. D., Rauniyar V., Hamilton G. L., Wu J., Toste F. D. Nature: 2011; 470 245
-
(2011)
Nature
, vol.470
, pp. 245
-
-
Shapiro, N.D.1
Rauniyar, V.2
Hamilton, G.L.3
Wu, J.4
Toste, F.D.5
-
330
-
-
64549094955
-
-
Beccalli E. M., Broggini G., Clerici F., Galli S., Kammerer C., Rigamonti M., Sottocornola S. Org. Lett.: 2009; 11 1563
-
(2009)
Org. Lett.
, vol.11
, pp. 1563
-
-
Beccalli, E.M.1
Broggini, G.2
Clerici, F.3
Galli, S.4
Kammerer, C.5
Rigamonti, M.6
Sottocornola, S.7
-
331
-
-
84950341314
-
-
Liu J., Han Z., Wang X., Wang Z., Ding K. J. Am. Chem. Soc.: 2015; 137 15346
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 15346
-
-
Liu, J.1
Han, Z.2
Wang, X.3
Wang, Z.4
Ding, K.5
-
338
-
-
80052321873
-
-
McDonald R. I., White P. B., Weinstein A. B., Tam C. P., Stahl S. S. Org. Lett.: 2011; 13 2830
-
(2011)
Org. Lett.
, vol.13
, pp. 2830
-
-
McDonald, R.I.1
White, P.B.2
Weinstein, A.B.3
Tam, C.P.4
Stahl, S.S.5
-
341
-
-
84857828738
-
-
Redford J. E., McDonald R. I., Rigsby M. L., Wiensch J. D., Stahl S. S. Org. Lett.: 2012; 14 1242
-
(2012)
Org. Lett.
, vol.14
, pp. 1242
-
-
Redford, J.E.1
McDonald, R.I.2
Rigsby, M.L.3
Wiensch, J.D.4
Stahl, S.S.5
-
345
-
-
77954242064
-
-
Exclusive formation of the anti diastereomer is observed in a more complex setting, see
-
Exclusive formation of the anti diastereomer is observed in a more complex setting, see: Qi X., Rice G. T., Lall M. S., Plummer M. S., White M. C. Tetrahedron: 2010; 66 4816
-
(2010)
Tetrahedron
, vol.66
, pp. 4816
-
-
Qi, X.1
Rice, G.T.2
Lall, M.S.3
Plummer, M.S.4
White, M.C.5
-
347
-
-
70350475266
-
-
Nahra F., Liron F., Prestat G., Mealli C., Messaoudi A., Poli G. Chem. Eur. J.: 2009; 15 11078
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 11078
-
-
Nahra, F.1
Liron, F.2
Prestat, G.3
Mealli, C.4
Messaoudi, A.5
Poli, G.6
-
349
-
-
38349004623
-
-
Liang C., Collet F., Robert-Peillard F., Müller P., Dodd R. H., Dauban P. J. Am. Chem. Soc.: 2008; 130 343
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 343
-
-
Liang, C.1
Collet, F.2
Robert-Peillard, F.3
Müller, P.4
Dodd, R.H.5
Dauban, P.6
-
350
-
-
84880924267
-
-
Darses B., Jarvis A. G., Mafroud A.-K, Estenne-Bouhtou G., Dargazanli G., Dauban P. Synthesis: 2013; 45 2079
-
(2013)
Synthesis
, vol.45
, pp. 2079
-
-
Darses, B.1
Jarvis, A.G.2
Mafroud, A.-K.3
Estenne-Bouhtou, G.4
Dargazanli, G.5
Dauban, P.6
|