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1
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84977687749
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This work appeared less than a decade after Diels' and Alder's first paper on their reaction. See also:
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Dane E., Höss O., Bindseil A.W., and Schmitt J. Liebigs Ann. Chem. 532 (1937) 39 This work appeared less than a decade after Diels' and Alder's first paper on their reaction. See also:
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Liebigs Ann. Chem.
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Dane, E.1
Höss, O.2
Bindseil, A.W.3
Schmitt, J.4
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2
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0011161194
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and references cited therein
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Dane E. Angew. Chem. 52 (1939) 655 and references cited therein
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Dane, E.1
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5
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0026716709
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Quinkert G., Del Grosso M., Bucher A., Döring W., Bauch M., Bats J.W., and Dürner G. Tetrahedron Lett. 33 (1992) 3617
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Quinkert, G.1
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Bauch, M.5
Bats, J.W.6
Dürner, G.7
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6
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0024500341
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For a related approach applied to the synthesis of certain abietanoid pigments, see:
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For a related approach applied to the synthesis of certain abietanoid pigments, see:. Lee J., and Snyder J.K. J. Am. Chem. Soc. 111 (1989) 1522
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Lee, J.1
Snyder, J.K.2
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7
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26844575469
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Saito N., Masuda M., Saito H., Takenouchi K., Ishizuka S., Namekawa J.-I., Takimoto-Kamimura M., and Kittaka A. Synthesis (2005) 2533
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Synthesis
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Saito, N.1
Masuda, M.2
Saito, H.3
Takenouchi, K.4
Ishizuka, S.5
Namekawa, J.-I.6
Takimoto-Kamimura, M.7
Kittaka, A.8
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11
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0035856630
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Aversa M.C., Barattucci A., Bonaccorsi P., Bruno G., Caruso F., and Giannetto P. Tetrahedron: Asymmetry 12 (2001) 2901
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(2001)
Tetrahedron: Asymmetry
, vol.12
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Aversa, M.C.1
Barattucci, A.2
Bonaccorsi, P.3
Bruno, G.4
Caruso, F.5
Giannetto, P.6
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13
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32044461762
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Angew. Chem. 113 (2001) 4198
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16
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1842483218
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For recent reviews on enyne metathesis which also include tandem RCEM/Diels-Alder processes, see:
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For recent reviews on enyne metathesis which also include tandem RCEM/Diels-Alder processes, see:. Diver S.T., and Giessert A.J. Chem. Rev. 104 (2004) 1317
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Chem. Rev.
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Diver, S.T.1
Giessert, A.J.2
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18
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15544374918
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Nair V., Sreekanth A.R., Abhilash N.P., Biju A.T.N., Varma L., Viji S., and Mathew S. ARKIVOC (2005) 178
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ARKIVOC
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Nair, V.1
Sreekanth, A.R.2
Abhilash, N.P.3
Biju, A.T.N.4
Varma, L.5
Viji, S.6
Mathew, S.7
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19
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0006300896
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Barjesteh H., Brain E.G., Charalambous J., Gaganatsou P., and Thomas T.A. J. Chem. Res. Synop. (1995) 454
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37049068386
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Mackenzie N.E., Surendrakumar S., Thomson R.H., Cowe H.J., and Cox P.J. J. Chem. Soc., Perkin Trans. 1 (1986) 2233
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37049119981
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Ansell M.F., Bignold A.J., Gosden A.F., Leslie V.J., and Murray R.A. J. Chem. Soc. (C) (1971) 1414
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33
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33846618754
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note
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The relative stereochemistry of the major diastereomeric adduct for the cycloadditions of (i) 5a with 6b and (ii) 4b with 11 were each chemically correlated. Thus silylation of 9b gave a compound identical to 10b. Desilylation of 8a gave a compound identical to 7a.
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35
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33646536570
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Prepared by anti-aldol addition of 1 to 2c followed by RCEM. For our new anti-aldol protocol see:
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Prepared by anti-aldol addition of 1 to 2c followed by RCEM. For our new anti-aldol protocol see:. Fraser B.H., Gelman D.M., Perlmutter P., and Vounatsos F. Tetrahedron: Asymmetry 17 (2006) 1152
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(2006)
Tetrahedron: Asymmetry
, vol.17
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Fraser, B.H.1
Gelman, D.M.2
Perlmutter, P.3
Vounatsos, F.4
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37
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0037154744
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Yadav V.K., Senthil G., Babu K.G., Parvez M., and Reid J.L. J. Org. Chem. 67 (2002) 1109
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Yadav, V.K.1
Senthil, G.2
Babu, K.G.3
Parvez, M.4
Reid, J.L.5
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39
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0001364053
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Das J., Dickinson R.A., Kakushima M., Kingston G.M., Reid G.R., Sato Y., and Valenta Z. Can. J. Chem. 62 (1984) 1103
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Das, J.1
Dickinson, R.A.2
Kakushima, M.3
Kingston, G.M.4
Reid, G.R.5
Sato, Y.6
Valenta, Z.7
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