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1
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0004145743
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VCH: Weinheim, in press
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Curran, D. P.; Porter, N. A.; Giese, B. Stereochemistry of Radical Reactions: Concepts, Guidelines and Synthetic Applications; VCH: Weinheim, in press
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Stereochemistry of Radical Reactions: Concepts, Guidelines and Synthetic Applications
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Curran, D.P.1
Porter, N.A.2
Giese, B.3
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3
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-
0001528625
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Recent examples
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Recent examples: Curran, D. P.; Chen, M.-H.; Kim, D. J. Am. Chem. Soc. 1989, 111, 6265.
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(1989)
J. Am. Chem. Soc.
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Curran, D.P.1
Chen, M.-H.2
Kim, D.3
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5
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0028089912
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Miura, K.; Itoh, D.; Hondo, T.; Hosomi, A. Tetrahedron Lett. 1994, 35, 9605.
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(1994)
Tetrahedron Lett.
, vol.35
, pp. 9605
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-
Miura, K.1
Itoh, D.2
Hondo, T.3
Hosomi, A.4
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6
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-
33751391738
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Kopping, B.; Chatgilialoglu, C.; Zehnder, M.; Giese, B. J. Org. Chem. 1992, 57, 3994.
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(1992)
J. Org. Chem.
, vol.57
, pp. 3994
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Kopping, B.1
Chatgilialoglu, C.2
Zehnder, M.3
Giese, B.4
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7
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-
84985582647
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Giese, B.; Gonzalez-Gomez, J. A.; Lachheim, S.; Metzger, J. O. Angew. Chem., Int. Ed. Engl. 1987, 26, 479.
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Angew. Chem., Int. Ed. Engl.
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Giese, B.1
Gonzalez-Gomez, J.A.2
Lachheim, S.3
Metzger, J.O.4
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8
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0027325392
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Haaima, G.; Lynch, M. J.; Routledge, A.; Weavers, R. T. Tetrahedron 1993, 49, 4229.
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(1993)
Tetrahedron
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, pp. 4229
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Haaima, G.1
Lynch, M.J.2
Routledge, A.3
Weavers, R.T.4
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9
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-
0001289004
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-
Chatgilialoglu, C.; Ballestri, M.; Ferreri C.; Vecchi, D. J. Org. Chem. 1995, 60, 3826.
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(1995)
J. Org. Chem.
, vol.60
, pp. 3826
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-
Chatgilialoglu, C.1
Ballestri, M.2
Ferreri, C.3
Vecchi, D.4
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10
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-
0000664747
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Curran, D. P.; Xu, J.; Lazzarini, E. J. Am. Chem. Soc. 1995, 117, 6603.
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(1995)
J. Am. Chem. Soc.
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, pp. 6603
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Curran, D.P.1
Xu, J.2
Lazzarini, E.3
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11
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-
85022625229
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in press
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Curran, D. P.; Xu, J.; Lazzarini, E. J. Chem. Soc, Perkin Trans. 1, in press
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J. Chem. Soc, Perkin Trans.
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Curran, D.P.1
Xu, J.2
Lazzarini, E.3
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17
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33845376338
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Curran, D. P.; Chen, M. H.; Kim, D. J. Am. Chem. Soc. 1986, 108, 2489.
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Curran, D.P.1
Chen, M.H.2
Kim, D.3
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19
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33847800833
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Precursors in entries 1, 2, 4, and 5 were prepared by methods analogous to those of Clive (ref 6). The precursor in entry 3 was prepared by acetylide addition to l-(2-(tetrahydropyranyloxy)ethyl)-cyclopentanone. See
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Precursors in entries 1, 2, 4, and 5 were prepared by methods analogous to those of Clive (ref 6). The precursor in entry 3 was prepared by acetylide addition to l-(2-(tetrahydropyranyloxy)ethyl)-cyclopentanone. See: Ashby, E. C.; Laemmle, J. T. Chem. Rev. 1975, 75, 521.
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(1975)
Chem. Rev.
, vol.75
, pp. 521
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-
Ashby, E.C.1
Laemmle, J.T.2
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21
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-
0011250203
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-
XH NMR spectra of the previously reported alcohols 17 and 18
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XH NMR spectra of the previously reported alcohols 17 and 18. Peijnenburg, W. J. G. M.; Buck, H. M. Tetrahedron 1988, 44, 4927.
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(1988)
Tetrahedron
, vol.44
, pp. 4927
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Peijnenburg, W.J.G.M.1
Buck, H.M.2
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