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Mori, K. In The Total Synthesis of Natural Products; ApSimon, J., Ed.; Wiley: New York, 1992; Vol. 9, pp 1-534.
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The Total Synthesis of Natural Products
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Mori, K.1
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Riba, M.5
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5
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0342339175
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note
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A search of the Science Citation Index showed >50 citations for the years 1987-1996. Significantly, the vast majority of papers citing this article used the method reported to prepare bromo alcohols. During the same period, ∼50% of the 1d → 2d conversions reported used this method.
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6
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0342774146
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See, for example: (a) Nakayama, T.; Mori, K. Liebigs Ann. / Recl. 1997, 839-843. (b) Kaiser, A.; Marazano, C.; Maier, M. J. Org. Chem. 1999, 64, 3778-3782. (c) Sharma, A.; Chattopadhyay, S. J. Org. Chem. 1998, 63, 6128-6131.
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(1997)
Liebigs Ann. / Recl.
, pp. 839-843
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Nakayama, T.1
Mori, K.2
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7
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0032927132
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See, for example: (a) Nakayama, T.; Mori, K. Liebigs Ann. / Recl. 1997, 839-843. (b) Kaiser, A.; Marazano, C.; Maier, M. J. Org. Chem. 1999, 64, 3778-3782. (c) Sharma, A.; Chattopadhyay, S. J. Org. Chem. 1998, 63, 6128-6131.
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(1999)
J. Org. Chem.
, vol.64
, pp. 3778-3782
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Kaiser, A.1
Marazano, C.2
Maier, M.3
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8
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0032483560
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See, for example: (a) Nakayama, T.; Mori, K. Liebigs Ann. / Recl. 1997, 839-843. (b) Kaiser, A.; Marazano, C.; Maier, M. J. Org. Chem. 1999, 64, 3778-3782. (c) Sharma, A.; Chattopadhyay, S. J. Org. Chem. 1998, 63, 6128-6131.
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(1998)
J. Org. Chem.
, vol.63
, pp. 6128-6131
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Sharma, A.1
Chattopadhyay, S.2
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10
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0026550975
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(b) Baldwin, J. E.; Adlington, R. M.; Ramcharitar, S. H. Tetrahedron 1992, 48, 3413-3428.
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(1992)
Tetrahedron
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, pp. 3413-3428
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Baldwin, J.E.1
Adlington, R.M.2
Ramcharitar, S.H.3
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12
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0000281301
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(b) Kulkarni, B. A.; Chattopadhyay, S.; Chattopadhyay, A.; Mamdapur, V. R. J. Org. Chem. 1993, 58, 5964-5966.
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(1993)
J. Org. Chem.
, vol.58
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Kulkarni, B.A.1
Chattopadhyay, S.2
Chattopadhyay, A.3
Mamdapur, V.R.4
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13
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0029055872
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(c) Börjesson, L.; Csöregh, I.; Welch, C. J. J. Org. Chem. 1995, 60, 2989-2999.
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(1995)
J. Org. Chem.
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Börjesson, L.1
Csöregh, I.2
Welch, C.J.3
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14
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0000529341
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Johansson, G.; Percec, V.; Ungar, G.; Zhou, J. P. Macromolecules 1996, 29, 646-660.
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(1996)
Macromolecules
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Johansson, G.1
Percec, V.2
Ungar, G.3
Zhou, J.P.4
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15
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0006287509
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When toluene was used in place of benzene (with a Dean-Stark trap), good yields of bromo alcohols were obtained but were contaminated with ca. 9% dibromides. (a) Enders, D.; Bartzen, D. Liebigs Ann. Chem. 1991, 569-574.
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(1991)
Liebigs Ann. Chem.
, pp. 569-574
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Enders, D.1
Bartzen, D.2
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17
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37049088904
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In the conversion of 1d to 2d, an additional 3 × 1 equiv of HBr was needed to achieve good conversion: Nakashima, H.; Hirata, N.; Iwamura, T.; Yamagiwa, Y.; Kamikawa, T. J. Chem. Soc., Perkin Trans. 1 1994, 2849-2857.
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(1994)
J. Chem. Soc., Perkin Trans. 1
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Nakashima, H.1
Hirata, N.2
Iwamura, T.3
Yamagiwa, Y.4
Kamikawa, T.5
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18
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0000252132
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See, for example: (a) McDougal, P. G.; Rico, J. G.; Oh, Y.-I.; Condon, B. D. J. Org. Chem. 1986, 51, 3388-3390. (b) Houille, O.; Schmittberger, T.; Uguen, D. Tetrahedron Lett. 1996, 37, 625-628.
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(1986)
J. Org. Chem.
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, pp. 3388-3390
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McDougal, P.G.1
Rico, J.G.2
Oh, Y.-I.3
Condon, B.D.4
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19
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0030065709
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See, for example: (a) McDougal, P. G.; Rico, J. G.; Oh, Y.-I.; Condon, B. D. J. Org. Chem. 1986, 51, 3388-3390. (b) Houille, O.; Schmittberger, T.; Uguen, D. Tetrahedron Lett. 1996, 37, 625-628.
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(1996)
Tetrahedron Lett.
, vol.37
, pp. 625-628
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Houille, O.1
Schmittberger, T.2
Uguen, D.3
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20
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0343644377
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note
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3NCl or Aliquat 336 to these reactions did not affect product distributions, suggesting that aqueous solubility is not a significant issue here.
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