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1
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0000036801
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Pergamon: Oxford
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1. Simpkins, N. S. Sulphones in Organic Synthesis; Pergamon: Oxford 1993. For a review of the chemistry of vinylic sulfones, See: Simpkins, N. S. Tetrahedron 1990, 46, 6951.
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(1993)
Sulphones in Organic Synthesis
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Simpkins, N.S.1
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2
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0000036801
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1. Simpkins, N. S. Sulphones in Organic Synthesis; Pergamon: Oxford 1993. For a review of the chemistry of vinylic sulfones, See: Simpkins, N. S. Tetrahedron 1990, 46, 6951.
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(1990)
Tetrahedron
, vol.46
, pp. 6951
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Simpkins, N.S.1
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4
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0026555217
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3. Craig, D.; Smith, A. M. Tetrahedron Lett. 1992, 33, 695; Craig, D.; Ikin, N. J.; Mathews, N.; Smith, A. M. Tetrahedron Lett. 1995, 36, 7531.
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Tetrahedron Lett.
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Craig, D.1
Smith, A.M.2
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5
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3. Craig, D.; Smith, A. M. Tetrahedron Lett. 1992, 33, 695; Craig, D.; Ikin, N. J.; Mathews, N.; Smith, A. M. Tetrahedron Lett. 1995, 36, 7531.
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, vol.36
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Craig, D.1
Ikin, N.J.2
Mathews, N.3
Smith, A.M.4
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6
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0029054699
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4. For studies on related cyclic systems, see: Kim, S. H.; Jin, Z. D.; Fuchs, P. L. Tetrahedron Lett. 1995, 36, 4537; Jin, Z. D.; Fuchs, P. L. J. Am. Chem. Soc. 1995, 117, 3022.
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Tetrahedron Lett.
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Kim, S.H.1
Jin, Z.D.2
Fuchs, P.L.3
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7
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0000204525
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4. For studies on related cyclic systems, see: Kim, S. H.; Jin, Z. D.; Fuchs, P. L. Tetrahedron Lett. 1995, 36, 4537; Jin, Z. D.; Fuchs, P. L. J. Am. Chem. Soc. 1995, 117, 3022.
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Jin, Z.D.1
Fuchs, P.L.2
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(ii) Tanaka, K.; Wakita, H.; Ioda, H.; Kuji, A. Chem. Lett. 1984, 1359;
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Tanaka, K.1
Wakita, H.2
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Kuji, A.4
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(v) Carretero, J. C.; De Lombaert, S.; Ghosez, L. Tetrahedron Lett. 1987, 28, 2135.
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De Lombaert, S.2
Ghosez, L.3
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13
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0026495588
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6. For a preliminary account of this work, see: Craig, D.; Etheridge, C. J.; Smith, A. M. Tetrahedron Lett. 1992, 33, 7445.
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(1992)
Tetrahedron Lett.
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Craig, D.1
Etheridge, C.J.2
Smith, A.M.3
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84972949066
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7. For an analogous one-pot method for the preparation of vinylic sulfones, see: Lee, J. W.; Oh, D. Y. Synth. Commun. 1989, 19, 2209; we thank a referee for bringing this work to our attention. For related methodology applied to the synthesis of vinylic sulfoxides and sulfoximines, see respectively: Craig, D.; Daniels, K.; Marsh, A.; Rainford, D.; Smith, A. M. Synlett 1990, 531, and Craig, D.; Geach, N. J. Synlett 1992, 299.
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(1989)
Synth. Commun.
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Lee, J.W.1
Oh, D.Y.2
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15
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33750249701
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7. For an analogous one-pot method for the preparation of vinylic sulfones, see: Lee, J. W.; Oh, D. Y. Synth. Commun. 1989, 19, 2209; we thank a referee for bringing this work to our attention. For related methodology applied to the synthesis of vinylic sulfoxides and sulfoximines, see respectively: Craig, D.; Daniels, K.; Marsh, A.; Rainford, D.; Smith, A. M. Synlett 1990, 531, and Craig, D.; Geach, N. J. Synlett 1992, 299.
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(1990)
Synlett
, pp. 531
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Craig, D.1
Daniels, K.2
Marsh, A.3
Rainford, D.4
Smith, A.M.5
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16
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0002256265
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7. For an analogous one-pot method for the preparation of vinylic sulfones, see: Lee, J. W.; Oh, D. Y. Synth. Commun. 1989, 19, 2209; we thank a referee for bringing this work to our attention. For related methodology applied to the synthesis of vinylic sulfoxides and sulfoximines, see respectively: Craig, D.; Daniels, K.; Marsh, A.; Rainford, D.; Smith, A. M. Synlett 1990, 531, and Craig, D.; Geach, N. J. Synlett 1992, 299.
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(1992)
J. Synlett
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Geach, N.2
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0001912005
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8. Mandai, T.; Moriyama, T.; Nakayama, Y.; Sugino, K.; Kawada, M.; Otera, J. Tetrahedron Lett. 1984, 25, 5913.
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Mandai, T.1
Moriyama, T.2
Nakayama, Y.3
Sugino, K.4
Kawada, M.5
Otera, J.6
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18
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0001434528
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9. We presume that the sulfone oxygen atoms rather than the α-carbon atom are in close proximity with the lithium counter-ion. See: Gaïs, H.-J.; Vollhardt, J.; Hellmann, G.; Paulus, H.; Lindner, H. J. Tetrahedron Lett. 1988, 29, 1259.
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(1988)
Tetrahedron Lett.
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Gaïs, H.-J.1
Vollhardt, J.2
Hellmann, G.3
Paulus, H.4
Lindner, H.J.5
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21
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0039273708
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12. 2-Benzyloxyethanal has been prepared using a variety of methods. See: (i) Palfray, S. Bull. Soc. Chim. Fr. 1937, 5, 950; Shiao, M.-J.; Yang, C.-Y.; Lee, S.-H.; Wu, T.-C. Synth. Commun. 1988, 18, 359 (oxidative cleavage of 3-benzyloxy-1,2-propanediol);
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(1937)
Bull. Soc. Chim. Fr.
, vol.5
, pp. 950
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Palfray, S.1
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22
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0001631888
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(oxidative cleavage of 3-benzyloxy-1,2-propanediol)
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12. 2-Benzyloxyethanal has been prepared using a variety of methods. See: (i) Palfray, S. Bull. Soc. Chim. Fr. 1937, 5, 950; Shiao, M.-J.; Yang, C.-Y.; Lee, S.-H.; Wu, T.-C. Synth. Commun. 1988, 18, 359 (oxidative cleavage of 3-benzyloxy-1,2-propanediol);
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(1988)
Synth. Commun.
, vol.18
, pp. 359
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Shiao, M.-J.1
Yang, C.-Y.2
Lee, S.-H.3
Wu, T.-C.4
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24
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3142632523
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ozone addition to benzyl vinyl ether followed by Zn-mediated reduction
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(iii) Danishefsky, S. J.; DeNinno, M. P. J. Org. Chem. 1986, 51, 2615 (ozone addition to benzyl vinyl ether followed by Zn-mediated reduction);
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J. Org. Chem.
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Danishefsky, S.J.1
DeNinno, M.P.2
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0026513813
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DIBAL-H-mediated reduction of methyl 2-benzyloxyacetate
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(iv) Kobayashi, Y.; Ito, Y.; Terashima, S. Tetrahedron 1992, 48; 55 (DIBAL-H-mediated reduction of methyl 2-benzyloxyacetate);
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(1992)
Tetrahedron
, vol.48
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Kobayashi, Y.1
Ito, Y.2
Terashima, S.3
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26
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0019989994
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activated DMSO-mediated oxidation of 2-benzyloxyethanol
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(v) Parry, R. J.; Naidu, M. V. J. Am. Chem. Soc. 1982, 104, 3217 (activated DMSO-mediated oxidation of 2-benzyloxyethanol);
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Parry, R.J.1
Naidu, M.V.2
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0027312320
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(ozonolytic cleavage of (Z)-1,4-bis(benzyloxy)-2-butene)
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(vi) Jones, K.; Storey, J. M. D. Tetrahedron 1993, 49, 4901-4906 (ozonolytic cleavage of (Z)-1,4-bis(benzyloxy)-2-butene);
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Tetrahedron
, vol.49
, pp. 4901-4906
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Jones, K.1
Storey, J.M.D.2
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28
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0039697372
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hydrolysis-oxidative cleavage of syn-1,2-bis(benzyloxymethyl)oxirane
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(vii) Garner, P.; Park, J. M. Synth. Commun. 1987, 17, 189 (hydrolysis-oxidative cleavage of syn-1,2-bis(benzyloxymethyl)oxirane.
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Synth. Commun.
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Garner, P.1
Park, J.M.2
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0026083128
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13. Craig, D.; Fischer, D. A.; Kemal, Ö.; Marsh, Plessner, T.; Slawin, A. M. Z.; Williams, D. J. Tetrahedron 1991, 47, 3095.
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(1991)
Tetrahedron
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Fischer, D.A.2
Kemal, O.3
Marsh, P.T.4
Slawin, A.M.Z.5
Williams, D.J.6
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14. Cid, P.; de March, P.; Figueredo, M.; Font, J.; Milán, S.; Soria, A.; Virgili, A. Tetrahedron 1993, 49, 3857.
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De March, P.2
Figueredo, M.3
Font, J.4
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18. Pecunioso, A.; Galoppini, E.; Menicagli, R. Tetrahedron 1990, 46, 7497.
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19. Takano, S.; Setoh, M.; Yamada, O.; Ogasawara, K. Synthesis 1993, 1253.
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20. Alexandre, C; Rouessac, F.; Tabti, B. Tetrahedron Lett. 1985, 26, 5453.
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Alexandre, C.1
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Tabti, B.3
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