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1
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For some recent papers reporting on different members of these families see: (a) S. Acherar, G. Audran, F. Cecchin and H. Monti, Tetrahedron, 2004, 60, 5907;
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1042264011
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(c) A. Srikrishna, N. C. Babu and M. S. Rao, Tetrahedron, 2004, 60, 2125;
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Srikrishna, A.1
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4
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0037424824
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(d) S. P. Chavan, R. K. Kharul, R. R. Kale and D. A. Khobragade, Tetrahedron, 2003, 59, 2737;
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0042063719
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(e) S. Acherar, G. Audran, N. Vanthuyne and H. Monti, Tetrahedron: Asymmetry, 2003, 14, 2413;
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Acherar, S.1
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0037455095
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(f) T. Paul, A. Pal, P. D. Gupta and D. Mukherjee, Tetrahedron Lett., 2003, 44, 737;
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Paul, T.1
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7
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0037421024
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(g) Y. Kita, J. Futamura, Y. Ohba, Y. Salama, J. K. Ganesh and H. Fujioka, Tetrahedron Lett., 2003, 44, 411;
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Kita, Y.1
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(h) T. Satoh, M. Yoshida, Y. Takahashi and H. Ota, Tetrahedron: Asymmetry, 2003, 14, 281;
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(i) B. R. Aavula, Q. Cui and E. A. Mash, Tetrahedron: Asymmetry, 2000, 11, 4681;
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(j) T. Poon, B. P. Mundy, F. G. Favaloro, C. A. Goudreau, A. Greenberg and R. Sullivan, Synthesis, 1998, 832.
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Poon, T.1
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12
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N. K. Ishikawa, K. Yamaji, S. Tahara, Y. Fukushi and K. Takahashi, Phytochemistry, 2000, 54, 777.
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Ishikawa, N.K.1
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K. Lal, I. Sharma, A. K. Agarwal, A. Agnihotri and S. Ray, J. Med. Chem., 1988, 31, 1261.
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14
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37049097737
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(a) R. D. Bowden, R. D. G. Cooper, C. J. Harris, G. P. Moss, B. C. L. Weedon and L. M. Jackman, J. Chem. Soc., Perkin Trans. 1, 1983, 1465;
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Ghosh, A.1
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(d) S. Samajdar, A. Ghatak and S. Ghosh, Tetrahedron Lett., 1999, 40, 4401;
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(e) S. Samajdar, A. Ghatak, S. Banerjee and S. Ghosh, Tetrahedron, 2001, 57, 2011.
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Samajdar, S.1
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19
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0003592858
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WA Benjamin, New York, 2nd edn., ch. 9
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H. O. House, Modern Synthetic Reactions, WA Benjamin, New York, 2nd edn., 1972, ch. 9;
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House, H.O.1
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0032500156
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K. Estieu, J. Ollivier and J. Salaun, Tetrahedron, 1998, 54, 8075.
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Estieu, K.1
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23
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0001112068
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(b) T. Cohen, L.-C. Yu and W. M. Daniewski, J. Org. Chem., 1985, 50, 4596;
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Cohen, T.1
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24
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0027968156
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For related ring expansion using Pd see: (c) H. Nemoto, M. Shiraki and K. Fukumoto, Tetrahedron, 1994, 50, 10391;
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Nemoto, H.1
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0000370802
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(d) H. Nemoto, J. Miyata, M. Yoshida, N. Raku and K. Fukumoto, J. Org. Chem., 1997, 62, 7850;
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Nemoto, H.1
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Fukumoto, K.5
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27
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0028856988
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For related iodonium ion-mediated ring expansion of olefinic cyclobutanols see: (f) H. Nemoto, M. Shiraki and K. Fukumoto, Tetrahedron Lett., 1995, 36, 8799;
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Nemoto, H.1
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0029863801
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(g) H. Nemoto, M. Shiraki and K. Fukumoto, J. Org. Chem., 1996, 61, 1347.
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A. M. Bernard, C. Floris, A. Frongia, P. P. Piras and F. Secci, Tetrahedron, 2004, 60, 449.
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Bernard, A.M.1
Floris, C.2
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Piras, P.P.4
Secci, F.5
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0042885928
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A. M. Bernard, E. Cadoni, A. Frongia, P. P. Piras and F. Secci, Org. Lett., 2002, 4, 2565.
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32
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33645197057
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-
note
-
9i was prepared from the corresponding lithium derivative obtained from 2-bromo-6-phenyl-1-hexene (see ESI†).
-
-
-
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33
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0000787875
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(a) H. Nemoto, H. Ishibashi, M. Nagamochi and K. Fukumoto, J. Org. Chem., 1992, 57, 1707;
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Nemoto, H.1
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Fukumoto, K.4
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34
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0007561834
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(b) For the synthesis of an analogous cyclobutanone following a different procedure see: K. Hiroi, H. Nakamura and T. Anzai, J. Am. Chem. Soc., 1987, 109, 1249.
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Hiroi, K.1
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Anzai, T.3
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0141631659
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A. M. Bernard, A. Frongia, P. P. Piras and F. Secci, Org. Lett., 2003, 5, 2923.
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Bernard, A.M.1
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Secci, F.4
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36
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0034705577
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A. M. Bernard, C. Floris, A. Frongia and P. P. Piras, Tetrahedron, 2000, 56, 4555.
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Bernard, A.M.1
Floris, C.2
Frongia, A.3
Piras, P.P.4
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37
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3042754041
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For a strictly related rearrangement see: N. Sarkar, A. Nayek and S. Ghosh, Org. Lett., 2004, 6, 1903.
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Sarkar, N.1
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