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1
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0032493026
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Ovaa, H.; Leeuwenburgh, M. A.; Overkleeft, H. S.; van der Marel, G. A.; van Boom, J. H. Tetrahedron Lett. 1998, 39, 3025.
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 3025
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Ovaa, H.1
Leeuwenburgh, M.A.2
Overkleeft, H.S.3
Van Der Marel, G.A.4
Van Boom, J.H.5
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2
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2342522136
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a) Leeuwenburgh, M. A.; Overkleeft, H. S.; van der Marel, G. A.; van Boom, J. H. Synlett 1997, 1263.
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(1997)
Synlett
, pp. 1263
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Leeuwenburgh, M.A.1
Overkleeft, H.S.2
Van Der Marel, G.A.3
Van Boom, J.H.4
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3
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0013580264
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in press
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b) Leeuwenburgh, M. A.; Kulker, C.; Duynstee, H. I.; Overkleeft, H. S.; van der Marel, G. A.; van Boom, J. H. Tetrahedron 1999, in press.
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(1999)
Tetrahedron
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Leeuwenburgh, M.A.1
Kulker, C.2
Duynstee, H.I.3
Overkleeft, H.S.4
Van Der Marel, G.A.5
Van Boom, J.H.6
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4
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0032514571
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van Hooft, P. A. V.; Leeuwenburgh, M. A.; Overkleeft, H. S.; van der Marel, G. A.; van Boeckel, C. A. A.; van Boom, J. H. Tetrahedron Lett. 1998, 39, 6061.
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 6061
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Van Hooft, P.A.V.1
Leeuwenburgh, M.A.2
Overkleeft, H.S.3
Van Der Marel, G.A.4
Van Boeckel, C.A.A.5
Van Boom, J.H.6
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8
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0032558611
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See for recently reported syntheses of carbocycles employing RCM on carbohydrate derivatives
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a) Ovaa, H.; Codée, J. D. C.; Lastdrager, B.; Overkleeft, H. S.; van der Marel, G. A.; van Boom, J. H. Tetrahedron Lett. 1998, 39, 7987. See for recently reported syntheses of carbocycles employing RCM on carbohydrate derivatives:
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 7987
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Ovaa, H.1
Codée, J.D.C.2
Lastdrager, B.3
Overkleeft, H.S.4
Van Der Marel, G.A.5
Van Boom, J.H.6
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9
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0033613678
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b) Sellier, O.; van de Weghe, P.; Le Nouen, D.; Strehler, C.; Eustache, J. Tetrahedron Lett. 1999, 40, 853.
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(1999)
Tetrahedron Lett.
, vol.40
, pp. 853
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Sellier, O.1
Van De Weghe, P.2
Le Nouen, D.3
Strehler, C.4
Eustache, J.5
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12
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0027438524
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b) Berger, D.; Overman, L. E.; Renhove, P. A. J. Am. Chem. Soc. 1993, 115, 9305.
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(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 9305
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Berger, D.1
Overman, L.E.2
Renhove, P.A.3
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16
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0013628223
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13C-NMR, MS) as well as elemental analysis
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13C-NMR, MS) as well as elemental analysis.
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18
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0013577769
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Vasella rearrangement of the p-methoxyphenyl galactoside 10 proved to be more effective than the corresponding methyl galactosides
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Vasella rearrangement of the p-methoxyphenyl galactoside 10 proved to be more effective than the corresponding methyl galactosides.
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20
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0027260325
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Gonda, J.; Helland, A.-C.; Ernst, B.; Bellus, D. Synthesis 1993, 729.
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(1993)
Synthesis
, pp. 729
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Gonda, J.1
Helland, A.-C.2
Ernst, B.3
Bellus, D.4
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21
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0001855961
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Schwab, P.; Grubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1996, 118, 100.
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(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 100
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Schwab, P.1
Grubbs, R.H.2
Ziller, J.W.3
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22
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0000238264
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Chida, N.; Tobe, T.; Murai, K.; Yamazaki, K.; Ogawa, S. Heterocycles 1994, 38, 2383.
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(1994)
Heterocycles
, vol.38
, pp. 2383
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Chida, N.1
Tobe, T.2
Murai, K.3
Yamazaki, K.4
Ogawa, S.5
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23
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0013631285
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14 in the palladium catalysed Overman rearrangement of (E, 4R)-4-(tert-butyloxycarbonylamino)-2-penten-1-ol
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14 in the palladium catalysed Overman rearrangement of (E, 4R)-4-(tert-butyloxycarbonylamino)-2-penten-1-ol.
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26
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0013628533
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18b, addition of HMPA (4 eq.) did not increase the yield
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18b, addition of HMPA (4 eq.) did not increase the yield.
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