-
3
-
-
0024835729
-
-
(c) Curran D.P., Chen M.-H., Spletzer E., Seong C.M., Chang C.-T. J. Am. Chem. Soc. 111:1989;8872-8878
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 8872-8878
-
-
Curran, D.P.1
Chen, M.-H.2
Spletzer, E.3
Seong, C.M.4
Chang, C.-T.5
-
4
-
-
0004269715
-
-
P. Renaud, Sibi M.P. Weinheim: Wiley-VCH. Chapter 1.5
-
(d) Byers J. Renaud P., Sibi M.P. Radicals in Organic Synthesis. Vol. 1:2001;Wiley-VCH, Weinheim. Chapter 1.5.
-
(2001)
Radicals in Organic Synthesis
, vol.1
-
-
Byers, J.1
-
5
-
-
0023757586
-
-
For an example using the transfer group for further transformation, see: Jolly R.S., Livinghouse T. J. Am. Chem. Soc. 110:1988;7536-7538.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 7536-7538
-
-
Jolly, R.S.1
Livinghouse, T.2
-
6
-
-
0032538355
-
-
For excellent reviews of Lewis acid application in radical reactions, see: (a) Renaud P., Gerster M. Angew. Chem. Int. Ed. Engl. 37:1998;2562-2579 (b) Sibi M.P., Porter N.A. Acc. Chem. Res. 32:1999;163-171.
-
(1998)
Angew. Chem. Int. Ed. Engl.
, vol.37
, pp. 2562-2579
-
-
Renaud, P.1
Gerster, M.2
-
7
-
-
0032960346
-
-
For excellent reviews of Lewis acid application in radical reactions, see: (a) Renaud P., Gerster M. Angew. Chem. Int. Ed. Engl. 37:1998;2562-2579 (b) Sibi M.P., Porter N.A. Acc. Chem. Res. 32:1999;163-171.
-
(1999)
Acc. Chem. Res.
, vol.32
, pp. 163-171
-
-
Sibi, M.P.1
Porter, N.A.2
-
8
-
-
0036625262
-
-
For excellent reviews on lanthanide triflates in organic synthesis, see: (a) Kobayashi S., Sugiura M., Kitagawa H., Lam W.W.-L. Chem. Rev. 102:2002;2227-2302 (b) Kobayashi S. Synlett. 1994;689-701. For examples about the application of Lewis acids such as lanthanide triflates in radical addition reactions or allylation reactions, see: (c) Sibi M.P., Ji J. J. Org. Chem. 61:1996;6090-6091 (d) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 35:1996;190-192 (e) Sibi M.P., Ji J. J. Am. Chem. Soc. 118:1996;3063-3064 (f) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 36:1997;274-276 (g) Sibi M.P., Rheault T.R. J. Am. Chem. Soc. 122:2000;8873-8879.
-
(2002)
Chem. Rev.
, vol.102
, pp. 2227-2302
-
-
Kobayashi, S.1
Sugiura, M.2
Kitagawa, H.3
Lam, W.W.-L.4
-
9
-
-
85064667331
-
-
For excellent reviews on lanthanide triflates in organic synthesis, see: (a) Kobayashi S., Sugiura M., Kitagawa H., Lam W.W.-L. Chem. Rev. 102:2002;2227-2302 (b) Kobayashi S. Synlett. 1994;689-701. For examples about the application of Lewis acids such as lanthanide triflates in radical addition reactions or allylation reactions, see: (c) Sibi M.P., Ji J. J. Org. Chem. 61:1996;6090-6091 (d) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 35:1996;190-192 (e) Sibi M.P., Ji J. J. Am. Chem. Soc. 118:1996;3063-3064 (f) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 36:1997;274-276 (g) Sibi M.P., Rheault T.R. J. Am. Chem. Soc. 122:2000;8873-8879.
-
(1994)
Synlett
, pp. 689-701
-
-
Kobayashi, S.1
-
10
-
-
0029814298
-
-
For excellent reviews on lanthanide triflates in organic synthesis, see: (a) Kobayashi S., Sugiura M., Kitagawa H., Lam W.W.-L. Chem. Rev. 102:2002;2227-2302 (b) Kobayashi S. Synlett. 1994;689-701. For examples about the application of Lewis acids such as lanthanide triflates in radical addition reactions or allylation reactions, see: (c) Sibi M.P., Ji J. J. Org. Chem. 61:1996;6090-6091 (d) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 35:1996;190-192 (e) Sibi M.P., Ji J. J. Am. Chem. Soc. 118:1996;3063-3064 (f) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 36:1997;274-276 (g) Sibi M.P., Rheault T.R. J. Am. Chem. Soc. 122:2000;8873-8879.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 6090-6091
-
-
Sibi, M.P.1
Ji, J.2
-
11
-
-
33748225421
-
-
For excellent reviews on lanthanide triflates in organic synthesis, see: (a) Kobayashi S., Sugiura M., Kitagawa H., Lam W.W.-L. Chem. Rev. 102:2002;2227-2302 (b) Kobayashi S. Synlett. 1994;689-701. For examples about the application of Lewis acids such as lanthanide triflates in radical addition reactions or allylation reactions, see: (c) Sibi M.P., Ji J. J. Org. Chem. 61:1996;6090-6091 (d) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 35:1996;190-192 (e) Sibi M.P., Ji J. J. Am. Chem. Soc. 118:1996;3063-3064 (f) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 36:1997;274-276 (g) Sibi M.P., Rheault T.R. J. Am. Chem. Soc. 122:2000;8873-8879.
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 190-192
-
-
Sibi, M.P.1
Ji, J.2
-
12
-
-
0001737502
-
-
For excellent reviews on lanthanide triflates in organic synthesis, see: (a) Kobayashi S., Sugiura M., Kitagawa H., Lam W.W.-L. Chem. Rev. 102:2002;2227-2302 (b) Kobayashi S. Synlett. 1994;689-701. For examples about the application of Lewis acids such as lanthanide triflates in radical addition reactions or allylation reactions, see: (c) Sibi M.P., Ji J. J. Org. Chem. 61:1996;6090-6091 (d) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 35:1996;190-192 (e) Sibi M.P., Ji J. J. Am. Chem. Soc. 118:1996;3063-3064 (f) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 36:1997;274-276 (g) Sibi M.P., Rheault T.R. J. Am. Chem. Soc. 122:2000;8873-8879.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 3063-3064
-
-
Sibi, M.P.1
Ji, J.2
-
13
-
-
0030903174
-
-
For excellent reviews on lanthanide triflates in organic synthesis, see: (a) Kobayashi S., Sugiura M., Kitagawa H., Lam W.W.-L. Chem. Rev. 102:2002;2227-2302 (b) Kobayashi S. Synlett. 1994;689-701. For examples about the application of Lewis acids such as lanthanide triflates in radical addition reactions or allylation reactions, see: (c) Sibi M.P., Ji J. J. Org. Chem. 61:1996;6090-6091 (d) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 35:1996;190-192 (e) Sibi M.P., Ji J. J. Am. Chem. Soc. 118:1996;3063-3064 (f) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 36:1997;274-276 (g) Sibi M.P., Rheault T.R. J. Am. Chem. Soc. 122:2000;8873-8879.
-
(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 274-276
-
-
Sibi, M.P.1
Ji, J.2
-
14
-
-
0034692362
-
-
For excellent reviews on lanthanide triflates in organic synthesis, see: (a) Kobayashi S., Sugiura M., Kitagawa H., Lam W.W.-L. Chem. Rev. 102:2002;2227-2302 (b) Kobayashi S. Synlett. 1994;689-701. For examples about the application of Lewis acids such as lanthanide triflates in radical addition reactions or allylation reactions, see: (c) Sibi M.P., Ji J. J. Org. Chem. 61:1996;6090-6091 (d) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 35:1996;190-192 (e) Sibi M.P., Ji J. J. Am. Chem. Soc. 118:1996;3063-3064 (f) Sibi M.P., Ji J. Angew. Chem. Int. Ed. Engl. 36:1997;274-276 (g) Sibi M.P., Rheault T.R. J. Am. Chem. Soc. 122:2000;8873-8879.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 8873-8879
-
-
Sibi, M.P.1
Rheault, T.R.2
-
17
-
-
0035812385
-
-
(a) Yang D., Gu S., Yan Y.-L., Zhu N.-Y., Cheung K.-K. J. Am. Chem. Soc. 123:2001;8612-8613.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 8612-8613
-
-
Yang, D.1
Gu, S.2
Yan, Y.-L.3
Zhu, N.-Y.4
Cheung, K.-K.5
-
18
-
-
0037119320
-
-
(b) Yang D., Gu S., Yan Y.-L., Zhao H.-W., Zhu N.-Y. Angew. Chem. Int. Ed. 41:2002;3014-3017.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 3014-3017
-
-
Yang, D.1
Gu, S.2
Yan, Y.-L.3
Zhao, H.-W.4
Zhu, N.-Y.5
-
21
-
-
0000150625
-
-
(c) Honda Y., Katayama S., Kojima M., Suzuki T., Izawa K. Org. Lett. 4:2002;447-449.
-
(2002)
Org. Lett.
, vol.4
, pp. 447-449
-
-
Honda, Y.1
Katayama, S.2
Kojima, M.3
Suzuki, T.4
Izawa, K.5
-
23
-
-
33845277902
-
-
For examples of α-halo β-keto esters in atom transfer radical reactions, see: (a) Hayes T.K., Villani R., Weinreb S.M. J. Am. Chem. Soc. 110:1988;5533-5543 (b) Curran D.P., Morgan T.M., Schwartz C.E., Snider B.B., Bombroski M.A. J. Am. Chem. Soc. 113:1991;6607-6617.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 5533-5543
-
-
Hayes, T.K.1
Villani, R.2
Weinreb, S.M.3
-
24
-
-
0001556501
-
-
For examples of α-halo β-keto esters in atom transfer radical reactions, see: (a) Hayes T.K., Villani R., Weinreb S.M. J. Am. Chem. Soc. 110:1988;5533-5543 (b) Curran D.P., Morgan T.M., Schwartz C.E., Snider B.B., Bombroski M.A. J. Am. Chem. Soc. 113:1991;6607-6617.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6607-6617
-
-
Curran, D.P.1
Morgan, T.M.2
Schwartz, C.E.3
Snider, B.B.4
Bombroski, M.A.5
-
25
-
-
33645559650
-
-
For examples of α-halo malonates in atom transfer radical reactions, see: (a) Curran D.P., Chang C.T. J. Org. Chem. 54:1989;3140-3157 (b) Flynn D.L., Zabrowski D.L. J. Org. Chem. 55:1990;3673-3674 (c) Curran D.P., Chang C.-T. Tetrahedron Lett. 31:1990;933-936.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 3140-3157
-
-
Curran, D.P.1
Chang, C.T.2
-
26
-
-
0000633408
-
-
For examples of α-halo malonates in atom transfer radical reactions, see: (a) Curran D.P., Chang C.T. J. Org. Chem. 54:1989;3140-3157 (b) Flynn D.L., Zabrowski D.L. J. Org. Chem. 55:1990;3673-3674 (c) Curran D.P., Chang C.-T. Tetrahedron Lett. 31:1990;933-936.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 3673-3674
-
-
Flynn, D.L.1
Zabrowski, D.L.2
-
27
-
-
0025022531
-
-
For examples of α-halo malonates in atom transfer radical reactions, see: (a) Curran D.P., Chang C.T. J. Org. Chem. 54:1989;3140-3157 (b) Flynn D.L., Zabrowski D.L. J. Org. Chem. 55:1990;3673-3674 (c) Curran D.P., Chang C.-T. Tetrahedron Lett. 31:1990;933-936.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 933-936
-
-
Curran, D.P.1
Chang, C.-T.2
-
28
-
-
0011211458
-
-
For the preparation of tert-butyl amine for substrate 1f , see: Padwa A., Kuethe J. J. Org. Chem. 63:1998;4256-4268.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 4256-4268
-
-
Padwa, A.1
Kuethe, J.2
-
29
-
-
0032769887
-
-
For Lewis acid promoted ionic cyclization of α-iodomalonates, see: (a) Kitagawa O., Taguchi T. Synlett. 1999;1191-1199 (b) Kitagawa O., Inoue T., Taguchi T. Tetrahedron Lett. 33:1992;2167-2170.
-
(1999)
Synlett
, pp. 1191-1199
-
-
Kitagawa, O.1
Taguchi, T.2
-
30
-
-
0026523472
-
-
For Lewis acid promoted ionic cyclization of α-iodomalonates, see: (a) Kitagawa O., Taguchi T. Synlett. 1999;1191-1199 (b) Kitagawa O., Inoue T., Taguchi T. Tetrahedron Lett. 33:1992;2167-2170.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 2167-2170
-
-
Kitagawa, O.1
Inoue, T.2
Taguchi, T.3
-
34
-
-
0023758737
-
-
(a) Konno K., Hashimoto K., Ohfune Y., Shirahama H., Matsumoto T. J. Am. Chem. Soc. 110:1988;4807-4815
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 4807-4815
-
-
Konno, K.1
Hashimoto, K.2
Ohfune, Y.3
Shirahama, H.4
Matsumoto, T.5
-
38
-
-
0037011395
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 4526-4529
-
-
Lei, A.1
Waldkirch, J.P.2
He, M.3
Zhang, X.4
-
39
-
-
0343237801
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 5212-5213
-
-
Jahn, U.1
Muller, M.2
Aussieker, S.3
-
40
-
-
0034614045
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 12007-12008
-
-
Trost, B.M.1
Pinkerton, A.B.2
Kremzow, D.3
-
41
-
-
0035958493
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 5237-5240
-
-
Duncan, D.1
Livinghouse, T.2
-
42
-
-
0035847256
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 169-174
-
-
Iwamoto, K.1
Kojima, M.2
Chatani, N.3
Murai, S.4
-
43
-
-
0035847216
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 315-319
-
-
Nagashima, H.1
Isono, Y.2
Iwamatsu, S.-I.3
-
44
-
-
0035831073
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 1861-1866
-
-
Francisco, C.G.1
Freire, R.2
Gonzalez, C.C.3
Leon, E.I.4
Riesco-Fagundo, C.5
Suarez, E.6
-
45
-
-
0037031692
-
-
For selected recent examples of γ-lactam syntheses, see: (a) Lei A., Waldkirch J.P., He M., Zhang X. Angew. Chem. Int. Ed. 41:2002;4526-4529 (b) Jahn U., Muller M., Aussieker S. J. Am. Chem. Soc. 122:2000;5212-5213 (c) Trost B.M., Pinkerton A.B., Kremzow D. J. Am. Chem. Soc. 122:2000;12007-12008 (d) Duncan D., Livinghouse T. J. Org. Chem. 66:2001;5237-5240 (e) Iwamoto K., Kojima M., Chatani N., Murai S. J. Org. Chem. 66:2001;169-174 (f) Nagashima H., Isono Y., Iwamatsu S.-I. J. Org. Chem. 66:2001;315-319 (g) Francisco C.G., Freire R., Gonzalez C.C., Leon E.I., Riesco-Fagundo C., Suarez E. J. Org. Chem. 66:2001;1861-1866 (h) Yoon C.H., Flanigan D.L., Chong B.-D., Jung K.W. J. Org. Chem. 67:2002;6582-6584.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 6582-6584
-
-
Yoon, C.H.1
Flanigan, D.L.2
Chong, B.-D.3
Jung, K.W.4
-
47
-
-
0034615528
-
-
Theoretical calculations indicated that cyclization via the trans pathway was lower in energy than the cis pathway. See: Clark A.J., Campo F.D., Deeth R.J., Filik R.P., Gatard S., Hunt N.A., Lastecoueres D., Thomas G.H., Verlhac J.-B., Wongtap H. J. Chem. Soc., Perkin Trans. 1. 2000;671-680.
-
(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 671-680
-
-
Clark, A.J.1
Campo, F.D.2
Deeth, R.J.3
Filik, R.P.4
Gatard, S.5
Hunt, N.A.6
Lastecoueres, D.7
Thomas, G.H.8
Verlhac, J.-B.9
Wongtap, H.10
-
51
-
-
0034697435
-
-
Norris T., Braish T.F., Butters M., DeVries K.M., Hawkins J.M., Massett S.S., Rose P.R., Santafianos D., Sklavounos C. J. Chem. Soc., Perkin Trans. 1. 2000;1615-1622.
-
(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 1615-1622
-
-
Norris, T.1
Braish, T.F.2
Butters, M.3
Devries, K.M.4
Hawkins, J.M.5
Massett, S.S.6
Rose, P.R.7
Santafianos, D.8
Sklavounos, C.9
-
52
-
-
0033593515
-
-
For examples of reported syntheses of 3-aza-2-bicyclo[3.1.0]hexan-2-one derivatives, see: (a) Zhang R., Mamai A., Madalengoitia J.S. J. Org. Chem. 64:1999;547-555 (b) Galeazzi R., Geremia S., Mobbili G., Orena M. Tetrahedron: Asymmetry. 7:1996;3573-3584 (c) Padwa A., Austin D.J., Price A.T. Tetrahedron Lett. 35:1994;7159-7162 (d) Chan S., Braish T.F. Tetrahedron. 50:1994;9943-9950 (e) Baldovini N., Bertrand M.-P., Carriere A., Nouguier R., Plancher J.-M. J. Org. Chem. 61:1996;3205-3208.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 547-555
-
-
Zhang, R.1
Mamai, A.2
Madalengoitia, J.S.3
-
53
-
-
0030561373
-
-
For examples of reported syntheses of 3-aza-2-bicyclo[3.1.0]hexan-2-one derivatives, see: (a) Zhang R., Mamai A., Madalengoitia J.S. J. Org. Chem. 64:1999;547-555 (b) Galeazzi R., Geremia S., Mobbili G., Orena M. Tetrahedron: Asymmetry. 7:1996;3573-3584 (c) Padwa A., Austin D.J., Price A.T. Tetrahedron Lett. 35:1994;7159-7162 (d) Chan S., Braish T.F. Tetrahedron. 50:1994;9943-9950 (e) Baldovini N., Bertrand M.-P., Carriere A., Nouguier R., Plancher J.-M. J. Org. Chem. 61:1996;3205-3208.
-
(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 3573-3584
-
-
Galeazzi, R.1
Geremia, S.2
Mobbili, G.3
Orena, M.4
-
54
-
-
0028059054
-
-
For examples of reported syntheses of 3-aza-2-bicyclo[3.1.0]hexan-2-one derivatives, see: (a) Zhang R., Mamai A., Madalengoitia J.S. J. Org. Chem. 64:1999;547-555 (b) Galeazzi R., Geremia S., Mobbili G., Orena M. Tetrahedron: Asymmetry. 7:1996;3573-3584 (c) Padwa A., Austin D.J., Price A.T. Tetrahedron Lett. 35:1994;7159-7162 (d) Chan S., Braish T.F. Tetrahedron. 50:1994;9943-9950 (e) Baldovini N., Bertrand M.-P., Carriere A., Nouguier R., Plancher J.-M. J. Org. Chem. 61:1996;3205-3208.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 7159-7162
-
-
Padwa, A.1
Austin, D.J.2
Price, A.T.3
-
55
-
-
0028137098
-
-
For examples of reported syntheses of 3-aza-2-bicyclo[3.1.0]hexan-2-one derivatives, see: (a) Zhang R., Mamai A., Madalengoitia J.S. J. Org. Chem. 64:1999;547-555 (b) Galeazzi R., Geremia S., Mobbili G., Orena M. Tetrahedron: Asymmetry. 7:1996;3573-3584 (c) Padwa A., Austin D.J., Price A.T. Tetrahedron Lett. 35:1994;7159-7162 (d) Chan S., Braish T.F. Tetrahedron. 50:1994;9943-9950 (e) Baldovini N., Bertrand M.-P., Carriere A., Nouguier R., Plancher J.-M. J. Org. Chem. 61:1996;3205-3208.
-
(1994)
Tetrahedron
, vol.50
, pp. 9943-9950
-
-
Chan, S.1
Braish, T.F.2
-
56
-
-
0029945337
-
-
For examples of reported syntheses of 3-aza-2-bicyclo[3.1.0]hexan-2-one derivatives, see: (a) Zhang R., Mamai A., Madalengoitia J.S. J. Org. Chem. 64:1999;547-555 (b) Galeazzi R., Geremia S., Mobbili G., Orena M. Tetrahedron: Asymmetry. 7:1996;3573-3584 (c) Padwa A., Austin D.J., Price A.T. Tetrahedron Lett. 35:1994;7159-7162 (d) Chan S., Braish T.F. Tetrahedron. 50:1994;9943-9950 (e) Baldovini N., Bertrand M.-P., Carriere A., Nouguier R., Plancher J.-M. J. Org. Chem. 61:1996;3205-3208.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 3205-3208
-
-
Baldovini, N.1
Bertrand, M.-P.2
Carriere, A.3
Nouguier, R.4
Plancher, J.-M.5
|