-
1
-
-
0003463148
-
-
For reviews, see: a, 3rd ed, Wiley: New York
-
For reviews, see: (a) Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 3rd ed.; Wiley: New York, 1999
-
(1999)
Protective Groups in Organic Synthesis
-
-
Greene, T.W.1
Wuts, P.G.M.2
-
3
-
-
33544465843
-
-
Kunakova, R. V.; Gaisin, R. L.; Sirazova, M. M.; Dzhemilev, U. M. Izv. Akad. Nauk SSSR Ser. Khim 1983, 32, 157-160.
-
(1983)
Izv. Akad. Nauk SSSR Ser. Khim
, vol.32
, pp. 157-160
-
-
Kunakova, R.V.1
Gaisin, R.L.2
Sirazova, M.M.3
Dzhemilev, U.M.4
-
4
-
-
33544465843
-
-
Kunakova, R. V.; Gaisin, R. L.; Sirazova, M. M.; Dzhemilev, U. M. Bull. Acad. Sci. USSR Div. Chem. Sci. (Engl. Transl.) 1983, 32, 157-160.
-
(1983)
Bull. Acad. Sci. USSR Div. Chem. Sci. (Engl. Transl.)
, vol.32
, pp. 157-160
-
-
Kunakova, R.V.1
Gaisin, R.L.2
Sirazova, M.M.3
Dzhemilev, U.M.4
-
5
-
-
67149136896
-
-
For reviews, see: (a) Simpkins, N. S. Sulfones in Organic Synthesis: Pergamon Press: New York. 1993
-
For reviews, see: (a) Simpkins, N. S. Sulfones in Organic Synthesis: Pergamon Press: New York. 1993
-
-
-
-
7
-
-
0001358368
-
-
Honda, M.; Morita, H.; Nagakura, I. J. Org. Chem. 1997, 62, 8932-8936.
-
(1997)
J. Org. Chem
, vol.62
, pp. 8932-8936
-
-
Honda, M.1
Morita, H.2
Nagakura, I.3
-
8
-
-
0028246489
-
-
(a) Chung, K. H.; Kim, J. N.; Ryu, E. K. Tetrahedron Lett. 1994, 35, 2913-2914
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 2913-2914
-
-
Chung, K.H.1
Kim, J.N.2
Ryu, E.K.3
-
9
-
-
0032552213
-
-
(b) Seong, M. R.; Lee, H. J.; Kim, J. N. Tetrahedron Lett. 1998, 39, 6219-6222
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 6219-6222
-
-
Seong, M.R.1
Lee, H.J.2
Kim, J.N.3
-
10
-
-
0032552142
-
-
(c) Lee, H. J.; Seong, M. R.; Kim, J. N. Tetrahedron Lett. 1998, 39, 6223-6226.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 6223-6226
-
-
Lee, H.J.1
Seong, M.R.2
Kim, J.N.3
-
11
-
-
31044438051
-
-
(a) Esquivias, J.; Gómez-Arrayás, R.; Carretero, J. C. Angew. Chem., Int. Ed. 2006, 45, 629-633
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 629-633
-
-
Esquivias, J.1
Gómez-Arrayás, R.2
Carretero, J.C.3
-
12
-
-
50149113699
-
-
(b) Alonso, I.; Esquivias, J.; Gómez-Arrayás, R.; Carretero, J. C. J. Org. Chem. 2008, 73, 6401-6404.
-
(2008)
J. Org. Chem
, vol.73
, pp. 6401-6404
-
-
Alonso, I.1
Esquivias, J.2
Gómez-Arrayás, R.3
Carretero, J.C.4
-
13
-
-
58449134253
-
-
Liu, C.-R.; Li, M.-B.; Yang, C.-F.; Tian, S.-K. Chem. - Eur, J. 2009, 15, 793-797.
-
(2009)
Chem. - Eur, J
, vol.15
, pp. 793-797
-
-
Liu, C.-R.1
Li, M.-B.2
Yang, C.-F.3
Tian, S.-K.4
-
14
-
-
40149107277
-
-
(a) Liu, C.-R.; Li, M.-B.; Yang, C.-F.; Tian, S.-K. Qhem. Commim. 2008, 1249-1251
-
(2008)
Qhem. Commim
, pp. 1249-1251
-
-
Liu, C.-R.1
Li, M.-B.2
Yang, C.-F.3
Tian, S.-K.4
-
16
-
-
34447326692
-
-
(c) Song, Q.-Y.; Yang, B.-L.; Tian, S.-K. J. Qrg. Chem. 2007, 72, 5407-5410.
-
(2007)
J. Qrg. Chem
, vol.72
, pp. 5407-5410
-
-
Song, Q.-Y.1
Yang, B.-L.2
Tian, S.-K.3
-
17
-
-
0344887064
-
-
2H is 7.1. See: Bordwell, F. G. Acc. Chem. Res. 1988, 21, 456-463.
-
2H is 7.1. See: Bordwell, F. G. Acc. Chem. Res. 1988, 21, 456-463.
-
-
-
-
18
-
-
0001097869
-
-
For a review, see: a, Trost, B. M, Fleming, I, Eds, Pergamon Press: Oxford
-
For a review, see: (a) Solladie, G. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991, Vol. 6, pp 133-170.
-
(1991)
Comprehensive Organic Synthesis
, vol.6
, pp. 133-170
-
-
Solladie, G.1
-
19
-
-
17444415379
-
-
For examples, see: b
-
For examples, see: (b) Wu, J.-P.; Emeigh, J.; Su, X.-P. Org. Lett. 2005, 7, 1223-1225
-
(2005)
Org. Lett
, vol.7
, pp. 1223-1225
-
-
Wu, J.-P.1
Emeigh, J.2
Su, X.-P.3
-
21
-
-
67149142191
-
-
1H NMR analysis of the reaction mixture.
-
1H NMR analysis of the reaction mixture.
-
-
-
-
22
-
-
67149138495
-
-
1H NMR analysis of the reaction mixture.
-
1H NMR analysis of the reaction mixture.
-
-
-
-
23
-
-
67149140014
-
-
For examples on the ambident nucleophilicity of sulfinate anions toward carbon electrophiles, see: (a) Reference 10b
-
For examples on the ambident nucleophilicity of sulfinate anions toward carbon electrophiles, see: (a) Reference 10b
-
-
-
-
24
-
-
0037288966
-
-
(b) Cacchi, S.; Fabrizi, G.; Goggiamani, A.; Parisi, L. M. Synlett 2003, 361-364
-
(2003)
Synlett
, pp. 361-364
-
-
Cacchi, S.1
Fabrizi, G.2
Goggiamani, A.3
Parisi, L.M.4
-
26
-
-
34347262098
-
-
For reviews on the preparation and application of such highly functionalized sulfonamides, see: a
-
For reviews on the preparation and application of such highly functionalized sulfonamides, see: (a) Masson, G.; Housseman, C.; Zhu, J. Angew. Chem., Int. Ed. 2007, 46, 4614-4628
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 4614-4628
-
-
Masson, G.1
Housseman, C.2
Zhu, J.3
-
27
-
-
59649098742
-
-
(b) Declerck, V.; Martinez, J.; Lamaty, F. Chem. Rev. 2009, 109, 1-48.
-
(2009)
Chem. Rev
, vol.109
, pp. 1-48
-
-
Declerck, V.1
Martinez, J.2
Lamaty, F.3
-
28
-
-
0038778548
-
-
For the stereoselective synthesis of trisubstituted allyl sulfones, see: a
-
For the stereoselective synthesis of trisubstituted allyl sulfones, see: (a) Kabalka, G. W.; Venkataiah, B.; Dong, G. Tetrahedron Lett. 2003, 44, 4673-4675
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 4673-4675
-
-
Kabalka, G.W.1
Venkataiah, B.2
Dong, G.3
-
29
-
-
33645282789
-
-
(b) Chandrasekhar, S.; Saritha, B.; Jagadeshwer, V.; Narsihmulu, C.; Vijay, D.; Sarma, G. D.; Jagadeesh, B. Tetrahedron Lett. 2006, 47, 2981-29847
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 2981-29847
-
-
Chandrasekhar, S.1
Saritha, B.2
Jagadeshwer, V.3
Narsihmulu, C.4
Vijay, D.5
Sarma, G.D.6
Jagadeesh, B.7
-
30
-
-
58249103011
-
-
(c) Reddy, L. R.; Hu, B.; Prashad, M.; Prasad, K. Angew. Chem., Int. Ed. 2009, 48, 172-174.
-
(2009)
Angew. Chem., Int. Ed
, vol.48
, pp. 172-174
-
-
Reddy, L.R.1
Hu, B.2
Prashad, M.3
Prasad, K.4
-
31
-
-
67149089094
-
-
The stereochemistry of new products 2v, 2w, and 2y was assigned by 2D NOESY analysis, and the stereochemistry of new product 2s was assigned by analogy. For details, see the Supporting Information.
-
The stereochemistry of new products 2v, 2w, and 2y was assigned by 2D NOESY analysis, and the stereochemistry of new product 2s was assigned by analogy. For details, see the Supporting Information.
-
-
-
|