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1
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Reviews: a
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Reviews: (a) Trost, B. M.; Toste, F. D.; Pinkerton, A. B. Chem. Rev. 2001, 101, 2067.
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Chem. Rev
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Trost, B.M.1
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2
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0036522941
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(b) Aubert, C.; Buisine, O.; Malacria, M. Chem. Rev. 2002, 102, 813.
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Chem. Rev
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Aubert, C.1
Buisine, O.2
Malacria, M.3
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3
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27544502994
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For a review of Alder ene reaction, see
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For a review of Alder ene reaction, see: Trost, B. M.; Frederiksen, M. U.; Rudd, M. T. Angew. Chem., Int. Ed. 2005, 44, 6630.
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(2005)
Angew. Chem., Int. Ed
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Trost, B.M.1
Frederiksen, M.U.2
Rudd, M.T.3
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5
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0000369431
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(b) Trost, B. M.; Indolese, A. F.; Müller, T. J. J.; Treptow, B. J. Am. Chem. Soc. 1995, 117, 615.
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J. Am. Chem. Soc
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Trost, B.M.1
Indolese, A.F.2
Müller, T.J.J.3
Treptow, B.4
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6
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0037123793
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(c) Trost, B. M.; Shen, H. C.; Pinkerton, A. B. Chem. - Eur. J. 2002, 10, 2341.
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Chem. - Eur. J
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Trost, B.M.1
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7
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0034658922
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(a) Trost, B. M.; Machacek, M.; Schnaderbeck, M. J. Org. Lett. 2000, 2, 1761.
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(2000)
Org. Lett
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Trost, B.M.1
Machacek, M.2
Schnaderbeck, M.J.3
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8
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0037122149
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(b) Trost, B. M.; Machacek, M. R. Angew. Chem., Int. Ed. 2002, 41, 4693.
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(2002)
Angew. Chem., Int. Ed
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Trost, B.M.1
Machacek, M.R.2
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9
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0041851126
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(c) Trost, B. M.; Machacek, M. R.; Ball, Z. T. Org. Lett. 2003, 5, 1895.
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Org. Lett
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Trost, B.M.1
Machacek, M.R.2
Ball, Z.T.3
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11
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0037144690
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Diynes were synthesized via a CuCl-catalyzed coupling reaction between terminal alkynes and 1-bromoalkynes: Marino, J. P.; Nguyen, H. N. J. Org. Chem. 2002, 67, 6841.
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Diynes were synthesized via a CuCl-catalyzed coupling reaction between terminal alkynes and 1-bromoalkynes: Marino, J. P.; Nguyen, H. N. J. Org. Chem. 2002, 67, 6841.
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12
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0030917961
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For regioselective metal-catalyzed intermolecular reactions involving multi-ynes, see: a
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For regioselective metal-catalyzed intermolecular reactions involving multi-ynes, see: (a) Takeda, A.; Ohno, A.; Kadota, I.; Gevorgyan, V.; Yamamoto, Y. J. Am. Chem. Soc. 1997, 119, 4547.
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J. Am. Chem. Soc
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Takeda, A.1
Ohno, A.2
Kadota, I.3
Gevorgyan, V.4
Yamamoto, Y.5
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13
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0032567182
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(b) Varela, J.; Castedo, L.; Saá, C. J. Am. Chem. Soc. 1998, 120, 12147.
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(1998)
J. Am. Chem. Soc
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Varela, J.1
Castedo, L.2
Saá, C.3
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14
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0000524141
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(c) Boring, E.; Sabat, M.; Finn, M. G.; Grimes, R. N. Organometallics 1998, 17, 3865.
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(1998)
Organometallics
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Boring, E.1
Sabat, M.2
Finn, M.G.3
Grimes, R.N.4
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15
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0034294451
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(d) Bredeau, S.; Delmas, G.; Pirio, N.; Richard, P.; Donnadieu, B.; Meunier, P. Organometallics 2000, 19, 4463.
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Organometallics
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Bredeau, S.1
Delmas, G.2
Pirio, N.3
Richard, P.4
Donnadieu, B.5
Meunier, P.6
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17
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0037065731
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(f) Camacho, D. H.; Saito, S.; Yamamoto, Y. J. Am. Chem. Soc. 2002, 124, 924.
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(2002)
J. Am. Chem. Soc
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Camacho, D.H.1
Saito, S.2
Yamamoto, Y.3
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18
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0000460189
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(g) Jeevanandam, A.; Korivi, R. P.; Huang, I.; Cheng, C. Org. Lett. 2002, 4, 807.
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(2002)
Org. Lett
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Jeevanandam, A.1
Korivi, R.P.2
Huang, I.3
Cheng, C.4
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19
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0141534442
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(h) Huddleston, R. R.; Jang, H.; Krische, M. J. J. Am. Chem. Soc. 2003, 125, 11488.
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(2003)
J. Am. Chem. Soc
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Huddleston, R.R.1
Jang, H.2
Krische, M.J.3
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21
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(j) Jiang, M. X.; Rawat, M.; Wulff, W. D. J. Am. Chem. Soc. 2004, 126, 5970.
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(2004)
J. Am. Chem. Soc
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Jiang, M.X.1
Rawat, M.2
Wulff, W.D.3
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22
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25144451317
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(k) Kim, M.; Miller, R. L.; Lee, D. J. Am. Chem. Soc. 2005, 127, 12818.
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(2005)
J. Am. Chem. Soc
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Kim, M.1
Miller, R.L.2
Lee, D.3
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24
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0001590841
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(a) Slugovc, C.; Ruba, E.; Schmid, R.; Kirchner, K.; Mereiter, K. Monatsh. Chem. 2000, 131, 1241.
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Monatsh. Chem
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Slugovc, C.1
Ruba, E.2
Schmid, R.3
Kirchner, K.4
Mereiter, K.5
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26
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29344448010
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Reactions with 1,3-diynes gave near completion within 5 min as opposed to 1-4 h for enynes: Trost, B. M.; Papillon, J. P. N.; Nussbaumer, T. J. Am. Chem. Soc. 2005, 127, 17921.
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Reactions with 1,3-diynes gave near completion within 5 min as opposed to 1-4 h for enynes: Trost, B. M.; Papillon, J. P. N.; Nussbaumer, T. J. Am. Chem. Soc. 2005, 127, 17921.
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0000510920
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Trost, B. M.; Müller, T. J. J.; Martinez, J. J. Am. Chem. Soc. 1995, 117, 1888.
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(1995)
J. Am. Chem. Soc
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Trost, B.M.1
Müller, T.J.J.2
Martinez, J.3
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28
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34249816213
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We believe that the lower reactivity of the borylated alkyne is caused by the electronic deactivation of boronate not by its steric hindrance
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We believe that the lower reactivity of the borylated alkyne is caused by the electronic deactivation of boronate not by its steric hindrance.
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30
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34249786925
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The preferred alkynyl substituent β to a metal in metallacyclobutenes formed from di- and triynes with metal carbenes; see refs 7j and 7k
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The preferred alkynyl substituent β to a metal in metallacyclobutenes formed from di- and triynes with metal carbenes; see refs 7j and 7k.
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31
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34249827929
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A total synthesis of (3R,9R, 10R)-panaxytriol utilizing Alder ene products 13o and 16b will be reported elsewhere.
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A total synthesis of (3R,9R, 10R)-panaxytriol utilizing Alder ene products 13o and 16b will be reported elsewhere.
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