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0038971573
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IICT Communication number 3423
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IICT Communication number 3423
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37049076524
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a) J.S. Yadav, T. Shekharam and V.R. Gadgil,. J. Chem. Soc. Chem. Commun., 1990, 843,
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J. Chem. Soc. Chem. Commun.
, vol.1990
, pp. 843
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Yadav, J.S.1
Shekharam, T.2
Gadgil, V.R.3
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9
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0039564657
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Selected references for the synthesis of 1-3 diols. a) K. Narasaka and H.C. Pai, Chem. Lett., 1980, 1415.
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Chem. Lett.
, vol.1980
, pp. 1415
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Narasaka, K.1
Pai, H.C.2
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11
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37049105156
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c) G. Cardillo, M. Orena, G. Porzi and S. Sandri, J. Chem. Soc. Chem. Commun., 1981, 465.
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J. Chem. Soc. Chem. Commun.
, vol.1981
, pp. 465
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Cardillo, G.1
Orena, M.2
Porzi, G.3
Sandri, S.4
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12
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0000507821
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and reference cited therein
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d) P.A. Bartlett, J.D. Meadows, E.G. Brown, A. Mon Moto and K.K. Jernstedt, J. Org. Chem., 47, 4013 (1982) and reference cited therein.
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(1982)
J. Org. Chem.
, vol.47
, pp. 4013
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Bartlett, P.A.1
Meadows, J.D.2
Brown, E.G.3
Mon Moto, A.4
Jernstedt, K.K.5
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13
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33845554880
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e) P. Ma, V.S. Martin, S. Masamune, K.B. Sharpless and S.M. Viti, J. Org. Chem., 47, 1378 (1982).
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(1982)
J. Org. Chem.
, vol.47
, pp. 1378
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Ma, P.1
Martin, V.S.2
Masamune, S.3
Sharpless, K.B.4
Viti, S.M.5
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18
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0001555040
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j) T. Nakata, S. Takao, M. Fukui, P. Tanaka and T. Oishi, Tetrahedron Lett., 23, 3873 (1983)
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(1983)
Tetrahedron Lett.
, vol.23
, pp. 3873
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Nakata, T.1
Takao, S.2
Fukui, M.3
Tanaka, P.4
Oishi, T.5
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0039564598
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(l) S. Kiyooka, H. Sasaoka, R. Fujiyama and C.K. Heathcock, Tetrahedron Lett. 25, 5331 (1984)
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(1984)
Tetrahedron Lett.
, vol.25
, pp. 5331
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Kiyooka, S.1
Sasaoka, H.2
Fujiyama, R.3
Heathcock, C.K.4
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23
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84987466985
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o) F.G. Kathawala, B. Prager, K. Prasad, O. Repic, M.J. Shapiro, R.S. Stabler and L. Widler, Helv. Chim-Acta 69, 803 (1986)
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(1986)
Helv. Chim-Acta
, vol.69
, pp. 803
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Kathawala, F.G.1
Prager, B.2
Prasad, K.3
Repic, O.4
Shapiro, M.J.5
Stabler, R.S.6
Widler, L.7
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33845374708
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p) K. Tamao, T. Nakajima, R. Sumiya, H. Arai, V. Higuchi and Y.J. Ito, J Am. Chem. Soc., 108, 6090 (1986).
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(1986)
J Am. Chem. Soc.
, vol.108
, pp. 6090
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Tamao, K.1
Nakajima, T.2
Sumiya, R.3
Arai, H.4
Higuchi, V.5
Ito, Y.J.6
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29
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0038971511
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note
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3), 1.15-1.34 (m, 10 H), 1.4 (s, 3H, acetonide), 1.45 (s, 3 H, acetonide), 1.6-1.8 (m, 2 H), 3.7-3.9 (m, 1 H), 4.24-4.38 (m, 1 H), 5.1 (d, J=8.8 Hz, 1 H), 5.25 (d, J=6.6 Hz, 1 H), 5.7-5.95 (m, 1 H). All new compounds are characterised by spectral data and HRMS.
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