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S. T. Perri, H. J. Dyke, H. W. Moore, J. Org. Chem. 1989, 54, 2032-2034;
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Perri, S.T.1
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A. Enhsen, K. Karabelas, J. M. Heerding, H. W. Moore, J. Org. Chem. 1990, 55, 1177-1185;
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Enhsen, A.1
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M. P. Winters, M. Stranberg, H. W. Moore, J. Org. Chem. 1994, 59, 7572-7574;
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Winters, M.P.1
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D. C. Harrowven, D. D. Pascoe, D. Demurtas, H. O. Bourne, Angew. Chem. 2005, 117, 1247-1248;
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Chem. Int. Ed
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F. Liu, L. S. Liebeskind, J. Org. Chem. 1998, 63, 2835-2844;
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9
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9644302331
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J. E. Ezcurra, K. Karabelas, H. W. Moore, Tetrahedron 2005, 61, 275-286.
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Tetrahedron
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Ezcurra, J.E.1
Karabelas, K.2
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0002225356
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For a review of the early literature, see, Ed, B. Halton, Jai Press, Grenwich, CT
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For a review of the early literature, see H. W. Moore, B. R. Yerxa in Advances in Strain in Organic Chemistry, Vol. 4 (Ed.: B. Halton), Jai Press, Grenwich, CT, 1995, pp. 81-162.
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Advances in Strain in Organic Chemistry
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Moore, H.W.1
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0030782938
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T. J. Onofrey, D. Gomez, M. Winters, H. W. Moore, J. Org. Chem. 1997, 62, 5658-5659;
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J. Org. Chem
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Onofrey, T.J.1
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0033515606
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R. Tiedemann, M. J. Heileman, H. W. Moore, J. Org. Chem. 1999, 64, 2170-2171;
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J. Org. Chem
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Tiedemann, R.1
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Moore, H.W.3
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R. Tiedemann, P. Turnbull, H. W. Moore, J. Org. Chem. 1999, 64, 4030-4041.
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J. Org. Chem
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Tiedemann, R.1
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D. Zhang, I. Llorente, L. S. Liebeskind, J. Org. Chem. 1997, 62, 4330-4338;
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Zhang, D.1
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0001290261
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Ed, B. M. Trost, I. Fleming, Pergamon, Oxford
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B. Snider in Comprehensive Organic Synthesis Vol. 2 (Ed.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, pp. 527-561;
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Comprehensive Organic Synthesis
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Snider, B.1
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27
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0032557215
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Cyclobutane 44 may be formed by an 8π electrocyclization of 43 followed by a 6π ring closure: M. J. Heileman, R. Tiedemann. H. W. Moore, J. Am. Chem. Soc. 1998, 120, 3801-3802.
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Cyclobutane 44 may be formed by an 8π electrocyclization of 43 followed by a 6π ring closure: M. J. Heileman, R. Tiedemann. H. W. Moore, J. Am. Chem. Soc. 1998, 120, 3801-3802.
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29
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33846407100
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Angew. Chem. Int. Ed. 1998, 37, 3340-3350: ;
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Chem. Int. Ed
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