-
3
-
-
33947283003
-
-
Hypervalent Iodine Chemistry; Wirth, T., Ed.; Topics in Current Chemistry 224; Springer: Berlin, 2003.
-
(c) Hypervalent Iodine Chemistry; Wirth, T., Ed.; Topics in Current Chemistry 224; Springer: Berlin, 2003.
-
-
-
-
6
-
-
33646083667
-
-
2, see: Celik, M.; Alp, C.; Coskun, B.; Gultekin, M. S.; Balci, M. Tetrahedron Lett. 2006, 47, 3659.
-
2, see: Celik, M.; Alp, C.; Coskun, B.; Gultekin, M. S.; Balci, M. Tetrahedron Lett. 2006, 47, 3659.
-
-
-
-
10
-
-
0037127560
-
-
(d) Ignacio, J.; Lena, C.; Altinel, E.; Birlirakis, N.; Arseniyadis, S. Tetrahedron Lett. 2002, 43, 1409.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 1409
-
-
Ignacio, J.1
Lena, C.2
Altinel, E.3
Birlirakis, N.4
Arseniyadis, S.5
-
11
-
-
46549096485
-
-
5-iodanes derived from glycols have been well characterized. See: (a) Frohn, H. J.; Pahlmann, W. J. Fluorine Chem. 1985, 28, 191.
-
5-iodanes derived from glycols have been well characterized. See: (a) Frohn, H. J.; Pahlmann, W. J. Fluorine Chem. 1985, 28, 191.
-
-
-
-
13
-
-
0000565339
-
-
(c) Munari, S. D.; Frigerio, M.; Santagostino, M. J. Org. Chem. 1996, 61, 9272.
-
(1996)
J. Org. Chem
, vol.61
, pp. 9272
-
-
Munari, S.D.1
Frigerio, M.2
Santagostino, M.3
-
14
-
-
33745487440
-
-
Beller, M, Bolm, C, Eds, Wiley-VCH: Weinheim
-
(a) Kuhn, F. E.; Fischer, R. W.; Herrmann, W. A.; Weskamp, T. In Transition Metals for Organic Synthesis; Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim, 2004; Vol. 2, p 427.
-
(2004)
Transition Metals for Organic Synthesis
, vol.2
, pp. 427
-
-
Kuhn, F.E.1
Fischer, R.W.2
Herrmann, W.A.3
Weskamp, T.4
-
15
-
-
0000036757
-
-
Trost, B. M, Fleming, I, Eds, Pergamon: Oxford
-
(b) Lee, D. G.; Chen, T. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 7, p 541.
-
(1991)
Comprehensive Organic Synthesis
, vol.7
, pp. 541
-
-
Lee, D.G.1
Chen, T.2
-
18
-
-
0032833625
-
-
Serious accidents due to explosions have been reported. See: a
-
Serious accidents due to explosions have been reported. See: (a) Koike, K.; Inoue, G.; Fukuda, T. J. Chem. Eng. Jpn. 1999, 32, 295.
-
(1999)
J. Chem. Eng. Jpn
, vol.32
, pp. 295
-
-
Koike, K.1
Inoue, G.2
Fukuda, T.3
-
19
-
-
33947233057
-
-
(b) Dorofeev, S. B.; Eletskii, A. V.; Smirnov, B. M. Sov. Phys. Dokl. 1981, 26, 318.
-
(1981)
Sov. Phys. Dokl
, vol.26
, pp. 318
-
-
Dorofeev, S.B.1
Eletskii, A.V.2
Smirnov, B.M.3
-
21
-
-
0037123252
-
-
(a) Travis, B. R.; Narayan, R. S.; Borhan, B. J. Am. Chem. Soc. 2002, 124, 3824.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 3824
-
-
Travis, B.R.1
Narayan, R.S.2
Borhan, B.3
-
23
-
-
27644509225
-
-
(c) Kogan, V.; Quintal, M. M.; Neumann, R. Org. Lett. 2005, 7, 5039.
-
(2005)
Org. Lett
, vol.7
, pp. 5039
-
-
Kogan, V.1
Quintal, M.M.2
Neumann, R.3
-
24
-
-
33947462653
-
-
(d) Pappo, R.; Allen, D. S.; Lemieux, R. U.; Johnson, W. S. J. Org. Chem. 1956, 21, 478.
-
(1956)
J. Org. Chem
, vol.21
, pp. 478
-
-
Pappo, R.1
Allen, D.S.2
Lemieux, R.U.3
Johnson, W.S.4
-
25
-
-
0142245594
-
-
(a) Ochiai, M.; Miyamoto, K.; Shiro, M.; Ozawa, T.; Yamaguchi, K. J. Am. Chem. Soc. 2003, 125, 13006.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 13006
-
-
Ochiai, M.1
Miyamoto, K.2
Shiro, M.3
Ozawa, T.4
Yamaguchi, K.5
-
26
-
-
11244278595
-
-
(b) Ochiai, M.; Miyamoto, K.; Yokota, Y.; Suefuji, T.; Shiro, M. Angew. Chem., Int. Ed. 2005, 44, 75.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 75
-
-
Ochiai, M.1
Miyamoto, K.2
Yokota, Y.3
Suefuji, T.4
Shiro, M.5
-
29
-
-
0009560590
-
-
Zhdankin, V. V.; Tykwinski, R.; Caple, R.; Berglund, B.; Koz'min, A. S.; Zefirov, N. S. Tetrahedron Lett. 1988, 29, 3703.
-
(1988)
Tetrahedron Lett
, vol.29
, pp. 3703
-
-
Zhdankin, V.V.1
Tykwinski, R.2
Caple, R.3
Berglund, B.4
Koz'min, A.S.5
Zefirov, N.S.6
-
30
-
-
0001505758
-
-
Richter, H. W.; Cherry, B. R.; Zook, T. D.; Koser, G. F. J. Am. Chem. Soc. 1997, 119, 9614.
-
(1997)
J. Am. Chem. Soc
, vol.119
, pp. 9614
-
-
Richter, H.W.1
Cherry, B.R.2
Zook, T.D.3
Koser, G.F.4
-
31
-
-
33845763473
-
-
3-Iodanes. See: Ochiai, M.; Sueda, T.; Miyamoto, K.; Kiprof, P.; Zhdankin, V. V. Angew. Chem., Int. Ed. 2006, 45, 8203.
-
3-Iodanes. See: Ochiai, M.; Sueda, T.; Miyamoto, K.; Kiprof, P.; Zhdankin, V. V. Angew. Chem., Int. Ed. 2006, 45, 8203.
-
-
-
-
32
-
-
0011965637
-
-
Cativiela, C.; Garcia, J. I.; Mayoral, J. A.; Salvatella, L. Can. J. Chem. 1994, 72, 308.
-
(1994)
Can. J. Chem
, vol.72
, pp. 308
-
-
Cativiela, C.1
Garcia, J.I.2
Mayoral, J.A.3
Salvatella, L.4
-
33
-
-
33947243151
-
-
Taft α value of solvent hydrogen-bond donor acidity of HFIP is 1.96. See: Reichardt, C. Solvents and Solvent Effects in Organic Chemistry; Wiley-VCH: Weinheim, Germany, 2003.
-
Taft α value of solvent hydrogen-bond donor acidity of HFIP is 1.96. See: Reichardt, C. Solvents and Solvent Effects in Organic Chemistry; Wiley-VCH: Weinheim, Germany, 2003.
-
-
-
-
34
-
-
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-
-
3-iodane 6b, being a more powerful oxidant than hydroxyiodane 6a (Figures S3 and S4).
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3-iodane 6b, being a more powerful oxidant than hydroxyiodane 6a (Figures S3 and S4).
-
-
-
-
35
-
-
0000493822
-
-
(a) Moriarty, R. M.; Khosrowshahi, J. S.; Prakash, O. Tetrahedron Lett. 1985, 26, 2961.
-
(1985)
Tetrahedron Lett
, vol.26
, pp. 2961
-
-
Moriarty, R.M.1
Khosrowshahi, J.S.2
Prakash, O.3
-
37
-
-
0001557651
-
-
(a) Moriarty, R. M.; Gupta, S. C.; Hu, H.; Berenschot, D. R.; White, K. B. J. Am. Chem. Soc. 1981, 103, 686.
-
(1981)
J. Am. Chem. Soc
, vol.103
, pp. 686
-
-
Moriarty, R.M.1
Gupta, S.C.2
Hu, H.3
Berenschot, D.R.4
White, K.B.5
-
38
-
-
0001127136
-
-
(b) Ochiai, M.; Nakanishi, A.; Suefuji, T. Org. Lett. 2000, 2, 2923.
-
(2000)
Org. Lett
, vol.2
, pp. 2923
-
-
Ochiai, M.1
Nakanishi, A.2
Suefuji, T.3
-
40
-
-
0342850245
-
-
For cleavage of 2-phenyloxirane with [bis(trifluoroacetoxy)iodo]benzene, see: Spyroudis, S.; Varvoglis, A. J. Org. Chem. 1981, 46, 5231.
-
For cleavage of 2-phenyloxirane with [bis(trifluoroacetoxy)iodo]benzene, see: Spyroudis, S.; Varvoglis, A. J. Org. Chem. 1981, 46, 5231.
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-
-
41
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The oxidative cleavage of aryloxiranes probably proceeds via the acid-catalyzed formation of intermediate vic-diols
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The oxidative cleavage of aryloxiranes probably proceeds via the acid-catalyzed formation of intermediate vic-diols.
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