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1
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0038322542
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Kakiuchi K., Okada H., Kanehisa N., Kai Y., and Kurosawa H. J. Org. Chem. 61 (1996) 2972-2979
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(1996)
J. Org. Chem.
, vol.61
, pp. 2972-2979
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-
Kakiuchi, K.1
Okada, H.2
Kanehisa, N.3
Kai, Y.4
Kurosawa, H.5
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2
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0033605838
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Gaini-Rahimi S., Steeneck C., Meyer I., Fitjer L., Pauer F., and Noltemeyer M. Tetrahedron 55 (1999) 3905-3916
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(1999)
Tetrahedron
, vol.55
, pp. 3905-3916
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Gaini-Rahimi, S.1
Steeneck, C.2
Meyer, I.3
Fitjer, L.4
Pauer, F.5
Noltemeyer, M.6
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3
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0000175470
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de Meijere A., Khlebnikov A.F., Kostikov R.R., Kozhushkov S.I., Schreiner P.R., Wittkopp A., and Yufit D.S. Angew. Chem. 111 (1999) 3682-3685
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(1999)
Angew. Chem.
, vol.111
, pp. 3682-3685
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de Meijere, A.1
Khlebnikov, A.F.2
Kostikov, R.R.3
Kozhushkov, S.I.4
Schreiner, P.R.5
Wittkopp, A.6
Yufit, D.S.7
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5
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0037084331
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de Meijere A., Khlebnikov A.F., Kozhushkov S.I., Kostikov R.R., Schreiner P.R., Wittkopp A., Rinderspacher C., Menzel H., Yufit D.S., and Howard J.A.K. Chem.-Eur. J. (2002) 828-842
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(2002)
Chem.-Eur. J.
, pp. 828-842
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de Meijere, A.1
Khlebnikov, A.F.2
Kozhushkov, S.I.3
Kostikov, R.R.4
Schreiner, P.R.5
Wittkopp, A.6
Rinderspacher, C.7
Menzel, H.8
Yufit, D.S.9
Howard, J.A.K.10
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6
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0038361043
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Fitjer L., Gerke R., Weiser J., Bunkoczi G., and Debreczeni J.E. Tetrahedron 59 (2003) 4443-4449
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(2003)
Tetrahedron
, vol.59
, pp. 4443-4449
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Fitjer, L.1
Gerke, R.2
Weiser, J.3
Bunkoczi, G.4
Debreczeni, J.E.5
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8
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16244373537
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de Meijere A., Khlebnikov A.F., Kozhushkov S.I., Miyazawa K., Frank D., Schreiner P.R., Rinderspacher C., Yufit D.S., and Howard J.A.K. Angew. Chem. 116 (2004) 6715-6719
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(2004)
Angew. Chem.
, vol.116
, pp. 6715-6719
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de Meijere, A.1
Khlebnikov, A.F.2
Kozhushkov, S.I.3
Miyazawa, K.4
Frank, D.5
Schreiner, P.R.6
Rinderspacher, C.7
Yufit, D.S.8
Howard, J.A.K.9
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9
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11144337859
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Angew. Chem. Int. Ed. 43 (2004) 6553-6557
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(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 6553-6557
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-
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10
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33746836922
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de Meijere A., Khlebnikov A.F., Kozhushkov S.I., Yufit D.S., Chetina O.V., Howard J.A.K., Kurahashi T., Mijazawa K., Frank D., Schreiner P.R., Rinderspacher B.C., Fujisawa M., Yamamoto C., and Okamoto Y. Chem.-Eur. J. (2006) 5697-5721
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(2006)
Chem.-Eur. J.
, pp. 5697-5721
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de Meijere, A.1
Khlebnikov, A.F.2
Kozhushkov, S.I.3
Yufit, D.S.4
Chetina, O.V.5
Howard, J.A.K.6
Kurahashi, T.7
Mijazawa, K.8
Frank, D.9
Schreiner, P.R.10
Rinderspacher, B.C.11
Fujisawa, M.12
Yamamoto, C.13
Okamoto, Y.14
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11
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36649011765
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Widjaja T., Fitjer L., Pal A., Schmidt H.-G., Noltemeyer M., Diedrich C., and Grimme S. J. Org. Chem. 72 (2007) 9264-9277
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(2007)
J. Org. Chem.
, vol.72
, pp. 9264-9277
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Widjaja, T.1
Fitjer, L.2
Pal, A.3
Schmidt, H.-G.4
Noltemeyer, M.5
Diedrich, C.6
Grimme, S.7
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12
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41549148995
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For an attempted synthesis of 6, see:
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For an attempted synthesis of 6, see:. Widjaja T., Fitjer L., Meindl K., and Herbst-Irmer R. Tetrahedron 64 (2008) 4304-4312
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(2008)
Tetrahedron
, vol.64
, pp. 4304-4312
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Widjaja, T.1
Fitjer, L.2
Meindl, K.3
Herbst-Irmer, R.4
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15
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58249107432
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For early reviews on methods for the construction of carbocyclic spiro compounds, see:
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For early reviews on methods for the construction of carbocyclic spiro compounds, see:
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19
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0034598046
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Compound 12 has first been prepared by Baldwin, et al.:
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Compound 12 has first been prepared by Baldwin, et al.:. Baldwin J.E., Keene M.E., and Shukla R. Tetrahedron Lett. 41 (2000) 9441-9443
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(2000)
Tetrahedron Lett.
, vol.41
, pp. 9441-9443
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Baldwin, J.E.1
Keene, M.E.2
Shukla, R.3
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20
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0011211276
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However, no experimental details were given. We therefore followed the general procedures given by Brady et al.:
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However, no experimental details were given. We therefore followed the general procedures given by Brady et al.:. Bak D.A., and Brady W.T.J. J. Org. Chem. (1979) 107-110
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(1979)
J. Org. Chem.
, pp. 107-110
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Bak, D.A.1
Brady, W.T.J.2
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21
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58249097985
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For an alternative approach, see:
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For an alternative approach, see:
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-
-
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27
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36649034171
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For cycloalkylations of α-quaternary cyclopentanones using potassium triethylcarbinolate and 1,4-dibromobutane, see:
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For cycloalkylations of α-quaternary cyclopentanones using potassium triethylcarbinolate and 1,4-dibromobutane, see:. Brugidou J., and Christol H. Bull. Soc. Chim. Fr. (1968) 1141-1144
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(1968)
Bull. Soc. Chim. Fr.
, pp. 1141-1144
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Brugidou, J.1
Christol, H.2
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30
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0001122966
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Methylenecyclopentane (bp 75-76 °C, yield 70%, purity 98% GC) was prepared as described for methylenecyclohexane:
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Methylenecyclopentane (bp 75-76 °C, yield 70%, purity 98% GC) was prepared as described for methylenecyclohexane:. Fitjer L., and Quabeck U. Synth. Commun. 15 (1985) 855-864
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(1985)
Synth. Commun.
, vol.15
, pp. 855-864
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Fitjer, L.1
Quabeck, U.2
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