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1
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3543085333
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For reviews, see: a, Moss, R. A, Platz, M, Jones, M, Eds, Wiley-Interscience: Hoboken, NJ
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For reviews, see: (a) Falvey, D. E. In Reactive Intermediate Chemistry; Moss, R. A., Platz, M., Jones, M., Eds.; Wiley-Interscience: Hoboken, NJ, 2004; p 593.
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Reactive Intermediate Chemistry
, pp. 593
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Falvey, D.E.1
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3
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0002802798
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For a theoretical treatment of this process, see
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For a theoretical treatment of this process, see: Hopkinson, A. C.; Lien, M. H.; Csizmadia, I. G.; Yates, K. Theor. Chim. Acta 1980, 55, 1.
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(1980)
Theor. Chim. Acta
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Hopkinson, A.C.1
Lien, M.H.2
Csizmadia, I.G.3
Yates, K.4
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4
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0026653993
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For the intermolecular reaction of O-stabilized nitrenium ions with alkenes, see: (a) Vedejs, E.; Sano, H. Tetrahedron Lett. 1992, 33, 3261.
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For the intermolecular reaction of O-stabilized nitrenium ions with alkenes, see: (a) Vedejs, E.; Sano, H. Tetrahedron Lett. 1992, 33, 3261.
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7
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47149103324
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For the reaction of N-stabilized nitrenium (or diazenium) ions with alkenes, see: (a) Tsukamoto, M.; Murata, K.; Sakamoto, T.; Saito, S.; Kikugawa, Y. Heterocycles 2008, 75, 1133.
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For the reaction of N-stabilized nitrenium (or diazenium) ions with alkenes, see: (a) Tsukamoto, M.; Murata, K.; Sakamoto, T.; Saito, S.; Kikugawa, Y. Heterocycles 2008, 75, 1133.
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8
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0012372787
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(b) Urry, W. H.; Szecsi, P.; Ikoku, C.; Moore, D. W. J. Am. Chem. Soc. 1964, 86, 2224.
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Urry, W.H.1
Szecsi, P.2
Ikoku, C.3
Moore, D.W.4
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9
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33846446683
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For the reaction of aryl nitrenium ions with alkenes, see: a
-
For the reaction of aryl nitrenium ions with alkenes, see: (a) Tellitu, I.; Urrejola, A.; Serna, S.; Moreno, I.; Herrero, M. T.; Domínguez, E.; SanMartin, R.; Correa, A. Eur. J. Org. Chem. 2007, 437.
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Eur. J. Org. Chem
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Tellitu, I.1
Urrejola, A.2
Serna, S.3
Moreno, I.4
Herrero, M.T.5
Domínguez, E.6
SanMartin, R.7
Correa, A.8
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10
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37049110828
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(b) Takeuchi, H.; Koyama, K.; Mitani, M.; Ihara, R.; Uno, T.; Okazaki, Y.; Kai, Y.; Kasai, N. J. Chem. Soc., Perkin Trans. 1 1985, 4, 677.
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J. Chem. Soc., Perkin Trans. 1
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Takeuchi, H.1
Koyama, K.2
Mitani, M.3
Ihara, R.4
Uno, T.5
Okazaki, Y.6
Kai, Y.7
Kasai, N.8
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11
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1542375289
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For a review, see
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For a review, see: Hu, X. E. Tetrahedron 2004, 60, 2701.
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Hu, X.E.1
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(c) Wardrop, D. J.; Zhang, W. M.; Landrie, C. L. Tetrahedron Lett. 2004, 45, 4229.
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Tetrahedron Lett
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Wardrop, D.J.1
Zhang, W.M.2
Landrie, C.L.3
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16
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84924255364
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Taken in part from: Forslund, R. E. Ph.D. Thesis, University of Illinois at Chicago, 2003.
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Taken in part from: Forslund, R. E. Ph.D. Thesis, University of Illinois at Chicago, 2003.
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17
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66149173396
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For selected intramolecular alkene oxaminations, see: a
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For selected intramolecular alkene oxaminations, see: (a) Donohoe, T. J.; Callens, C. K. A.; Thompson, A. L. Org. Lett. 2009, 11, 2305.
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Org. Lett
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Donohoe, T.J.1
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Thompson, A.L.3
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(b) Fuller, P. H.; Kim, J.-W.; Chemler, S. R. J. Am. Chem. Soc. 2008, 130, 17638.
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J. Am. Chem. Soc
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Fuller, P.H.1
Kim, J.-W.2
Chemler, S.R.3
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(d) Alexanian, E. J.; Lee, C.; Sorensen, E. J. J. Am. Chem. Soc. 2005, 127, 7690.
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J. Am. Chem. Soc
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Alexanian, E.J.1
Lee, C.2
Sorensen, E.J.3
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21
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0343857225
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These reagents mediate hydrazine formation. See
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These reagents mediate hydrazine formation. See: De Almeida, M. V.; Barton, D. H. R.; Bytheway, I.; Ferreira, J. A.; Hall, M. B.; Liu, W.; Taylor, D. K.; Thomson, L. J. Am. Chem. Soc. 1995, 117, 4870.
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De Almeida, M.V.1
Barton, D.H.R.2
Bytheway, I.3
Ferreira, J.A.4
Hall, M.B.5
Liu, W.6
Taylor, D.K.7
Thomson, L.8
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22
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69049094962
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For Pb(IV)-mediated formation of bridged aziridines, see: Hu, H.; Faraldos, J. A.; Coates, R. M. J. Am. Chem. Soc. 2009, 131, 11998.
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For Pb(IV)-mediated formation of bridged aziridines, see: Hu, H.; Faraldos, J. A.; Coates, R. M. J. Am. Chem. Soc. 2009, 131, 11998.
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23
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33947294377
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For β-opening of bicyclic aziridinium and epoxonium ions, see: a
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For β-opening of bicyclic aziridinium and epoxonium ions, see: (a) Leonard, N. J.; Dixon, D. B. J. Org. Chem. 1970, 35, 3483.
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(1970)
J. Org. Chem
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Leonard, N.J.1
Dixon, D.B.2
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24
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34347264054
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(b) Wan, S.; Gunaydin, H.; Houk, K. N.; Floreancig, P. E. J. Am. Chem. Soc. 2007, 129, 7915.
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J. Am. Chem. Soc
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Wan, S.1
Gunaydin, H.2
Houk, K.N.3
Floreancig, P.E.4
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26
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0000883386
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(b) Williams, D. R.; Osterhout, M. H.; McGill, J. M. Tetrahedron Lett. 1989, 30, 1331.
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Tetrahedron Lett
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Williams, D.R.1
Osterhout, M.H.2
McGill, J.M.3
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27
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0000455929
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Loudon, G. M.; Radhakrishna, A. S.; Almond, M. R.; Blodgett, J. K.; Boutin, R. H. J. Org. Chem. 1984, 49, 4272.
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J. Org. Chem
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Loudon, G.M.1
Radhakrishna, A.S.2
Almond, M.R.3
Blodgett, J.K.4
Boutin, R.H.5
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32
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84924230539
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That in this case the approach of the alkene to the N-center may be intimately involved with, and assist in, the departure of the protonated trifluoroacetate group is not discounted.
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That in this case the approach of the alkene to the N-center may be intimately involved with, and assist in, the departure of the protonated trifluoroacetate group is not discounted.
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33
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33646083667
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For an example of this process, see
-
For an example of this process, see: Celik, M.; Alp, C.; Coskun, B.; Gütekin, M. S.; Balci, M. Tetrahedron Lett. 2006, 47, 3659.
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(2006)
Tetrahedron Lett
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Celik, M.1
Alp, C.2
Coskun, B.3
Gütekin, M.S.4
Balci, M.5
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34
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84924251156
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Reductive cleavage of N-methoxy lactams to the corresponding lactams can be accomplished with range of reducing agents, including Mo(CO) 6 see ref 7, For experimental details, see the Supporting Information
-
6 (see ref 7). For experimental details, see the Supporting Information.
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