Organic Letters
Letter
Rudolph, M.; Rominger, F. Chem.− Eur. J. 2011, 17, 8195−8201.
(d) Teo, W. T.; Rao, W.; Ng, C. J. H.; Koh, S. W. Y.; Chan, P. W. H. Org.
Lett. 2014, 16, 1248−1251.
(10) Selected examples: (a) Cho, S. H.; Liebeskind, L. J. Org. Chem.
1987, 52, 2631−2634. (b) Wender, P. A.; Gamber, G. G.; Hubbard, R.
D.; Pham, S. M.; Zhang, L. J. Am. Chem. Soc. 2005, 127, 2836−2837.
(c) Padwa, A.; Xu, S. J. Am. Chem. Soc. 1992, 114, 5881−5882.
(11) Selected examples: (a) Danishefsky, S.; Kitahara, T.; Yan, C. F.;
Morris, J. J. Am. Chem. Soc. 1979, 101, 6996−11554. (b) Danheiser, R.
L.; Sard, H. J. Org. Chem. 1980, 45, 4810−4812. (c) Obrecht, D. Helv.
Chim. Acta 1991, 74, 27−46. (d) Kita, Y.; Okunaka, R.; Honda, T.;
Shindo, M.; Taniguchi, M.; Kondo, M.; Sasho, M. J. Org. Chem. 1991, 56,
119−125. (e) Hashmi, A. S. K.; Frost, T. M.; Bats, J. W. J. Am. Chem. Soc.
2000, 122, 11553−11554. See also: (f) Saito, S.; Yamamoto, Y. Chem.
Rev. 2000, 100, 2901−2916.
(12) Selected examples: (a) Hanson, G. A. Bull. Soc. Chim. Belg. 1956,
65, 1024−1034. (b) Chan, T.-H.; Brownbridge, P. J. Am. Chem. Soc.
1980, 102, 3534−3538. (c) Tius, M. A.; Thurkauf, A.; Truesdell, J. W.
Tetrahedron Lett. 1982, 23, 2819−2822. (d) Eichinger, K.; Nussbaumer,
P.; Balkan, S.; Schulz, G. Synthesis 1987, 1061−1064. (e) Smith, A. B.;
Kilenyi, S. N. Tetrahedron Lett. 1985, 26, 4419−4422. (f) Lefebvre, O.;
Brigaud, T.; Portella, C. Tetrahedron 1998, 22, 5839−5948. (g) Barton,
D. H. R.; Dressaire, G.; Willis, B. J.; Barrett, A. G. M.; Pfeffer, M. J. Chem.
Soc., Perkin Trans. 1 1982, 665−669. (h) Langer, P.; Bose, G. Angew.
Chem., Int. Ed. 2003, 42, 4033−4036. (i) Feist, H.; Langer, P. Synthesis
2007, 327−347. (j) Buttner, S.; Lubbe, M.; Reinke, H.; Fischer, C.;
Langer, P. Tetrahedron 2008, 54, 7968−7976. (j) Samshuddin, S.;
Narayana, B.; Sarojini, B. K. Molbank 2011, M745. (k) Poudel, T. N.;
Lee, Y. R. Org. Biomol. Chem. 2014, 12, 919−930.
(13) Selected examples: (a) Marx, J. N.; Argyle, J. C.; Norman, L. R. J.
Am. Chem. Soc. 1974, 96, 2121−2129. (b) King, R. R. J. Org. Chem. 1979,
44, 4194−4195. (c) Miller, B. J. Org. Chem. 1977, 42, 1402−1408.
(14) Selective papers: (a) Ivanov, C.; Tcholakova, T. Synthesis 1981,
392−394. (b) Hegde, S. G.; Kassim, A. M.; Kennedy, A. I. Tetrahedron
2001, 57, 1689−1698. (c) Izawa, Y.; Pun, D.; Stahl, S. S. Science 2011,
333, 209−213. (d) Kessler, M. T.; Prechtl, M. H. G. ChemCatChem.
2012, 4, 326−327.
(15) Selected examples: (a) Boger, D. L.; Mullican, M. D. J. Org. Chem.
1984, 49, 4045−4050. (b) Katritzky, A. R.; Belyakov, S. A.; Fang, Y.;
Kiely, J. S. Tetrahedron Lett. 1998, 39, 8051−8054. (c) Bi, X.; Dong, D.;
Liu, Q.; Pan, Wei; Zhao, L.; Li, B. J. Am. Chem. Soc. 2005, 127, 4578−
4579.
(16) Yi, W.-B.; Zhang, Z.; Huang, X.; Tanner, A.; Cai, C.; Zhang, W.
RSC Adv. 2013, 3, 18267−18270.
(17) Yi, W.-B.; Huang, X.; Cai, C.; Zhang, W. Green Chem. 2012, 14,
3185−3189.
(18) In the presense of fluorination agent Selectfluor and its derivative,
the dehydrofluorination cannot be processed efficiently.
(19) (a) Katritzky, A. R.; Belyakov, S. A.; Henderson, S. A. J. Org. Chem.
1997, 62, 8215−8217. (b) Rao, H. S. P.; Senthilkumar, S. P. J. Org. Chem.
2004, 69, 2591−2594.
(20) (a) Dolbier, W. R., Jr.; Keaffaber, J. J.; Burkholer, C. R.
Tetrahedron 1992, 48, 9649−9660. (b) Lefebvre, O.; Brigaud, T.;
Portella, C. Tetrahedron 1998, 54, 5939−4948. (c) Chanteau, F.;
Plantier-Royon, R.; Haufe, G.; Portella, C. Tetrahedron 2006, 62, 9049−
9053. (d) Surmont, R.; Verniest, G.; Colpaert, F.; Macdonald, G.;
Thuring, J. W.; Deroose, F.; De Kimpe, N. J. Org. Chem. 2009, 74, 1377−
1380. (e) Massicot, F.; Iriarte, A. M.; Brigaud, T.; Lebrun, A.; Portella, C.
Org. Biomol. Chem. 2011, 9, 600−603.
(21) Hussain, I.; Yawer, M. A.; Lau, M.; Pundt, T.; Fischer, C.; Gorls,
̈
H.; Langer, P. Eur. J. Org. Chem. 2008, 503−518.
(22) Samant, B. S.; Bhagwat, S. S. Appl. Catal. A: Gen. 2011, 394, 191−
194.
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