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(PhI(OH)OTs). These techniques, however, are unsuitable for the conduct of tandem oxidative amidation/intramolecular nitrile oxide cycloaddition sequences (see text and ref 6)
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Raihan, M. J.; Kavala, V.; Kuo, C.-W.; Rama Raju, B.; Yao, C. F. Green Chem. 2010, 12, 1090 (PhI(OH)OTs). These techniques, however, are unsuitable for the conduct of tandem oxidative amidation/intramolecular nitrile oxide cycloaddition sequences (see text and ref 6)
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Recent developments:; J. Org. Chem. 2008, 4299
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Ciufolini, M. A.; Braun, N. A.; Canesi, S.; Ousmer, M.; Chang, J.; Chai, D. Synthesis 2007, 3759 Recent developments: Liang, H.; Ciufolini, M. A. J. Org. Chem. 2008, 73, 4299
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Liang, H.; Ciufolini, M. A. Chem.-Eur. J. 2010, 16, 13262 See also: Braun, N. A.; Ciufolini, M. A.; Peters, K.; Peters, E.-M. Tetrahedron Lett. 1998, 39, 4667
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Braun, N. A.; Bray, J.; Ciufolini, M. A. Tetrahedron Lett. 1999, 40, 4985
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Braun, N. A.; Bray, J.; Ousmer, M.; Peters, K.; Peters, E.-M.; Bouchu, D.; Ciufolini, M. A. J. Org. Chem. 2000, 65, 4397
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Canesi, S.; Belmont, P.; Bouchu, D.; Rousset, L.; Ciufolini, M. A. Tetrahedron Lett. 2002, 43, 5193
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Reviews on intramolecular nitrile oxide cycloadditions: In;;;;;, Eds.; VCH: Weinheim, Germany,; Vol., p
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Reviews on intramolecular nitrile oxide cycloadditions: Mulzer, J. In Organic Synthesis Highlights; Mulzer, J.; Altenbach, H. J.; Braun, M.; Krohn, K.; Reissig, H. U., Eds.; VCH: Weinheim, Germany, 1990; Vol. I, p 77.
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70349906431
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4736. The methodology also enables the conduct of oxidative phenolic alkoxylation/INOC sequences
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Mendelsohn, B. A.; Ciufolini, M. A. Org. Lett. 2009, 11, 4736. The methodology also enables the conduct of oxidative phenolic alkoxylation/INOC sequences
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39
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78651504831
-
-
Commercially available
-
Commercially available.
-
-
-
-
40
-
-
0342347015
-
-
Prepared according to
-
Prepared according to: Cope, A. C.; Estes, L. L., Jr.; Emery, J. R.; Haven, A. C., Jr. J. Am. Chem. Soc. 1951, 73, 1199
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Cope, A.C.1
Estes Jr., L.L.2
Emery, J.R.3
Haven Jr., A.C.4
-
41
-
-
78651520901
-
-
Prepared according to: US 19610919 (CAS No. 61:83839). Details are provided as Supporting Information
-
Prepared according to: Werber, F. X. US 19610919 (CAS No. 61:83839). Details are provided as Supporting Information.
-
-
-
Werber, F.X.1
-
42
-
-
85027853920
-
-
Prepared according to
-
Prepared according to: Chen, Y. K.; Jeon, S.-J.; Walsh, P. J.; Nugent, W. A. Org. Synth. 2005, 82, 87
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(2005)
Org. Synth.
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Chen, Y.K.1
Jeon, S.-J.2
Walsh, P.J.3
Nugent, W.A.4
-
44
-
-
0002691473
-
-
Prepared according to
-
Prepared according to: Rodionov, V. M.; Machinskaya, I. V.; Belikov, V. M. Zh. Obshch. Khim. 1948, 18, 917
-
(1948)
Zh. Obshch. Khim.
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Rodionov, V.M.1
MacHinskaya, I.V.2
Belikov, V.M.3
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46
-
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0000604457
-
-
Prepared according to
-
Prepared according to: Zolfigol, M. A. Molecules 2001, 6, 694
-
(2001)
Molecules
, vol.6
, pp. 694
-
-
Zolfigol, M.A.1
-
47
-
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78651473394
-
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Because of such poor yields, compounds 29 and 30 were not fully characterized
-
Because of such poor yields, compounds 29 and 30 were not fully characterized.
-
-
-
-
49
-
-
34548784461
-
-
references cited therein
-
Machetti, F.; Cecchi, L.; Trogu, E.; De Sarlo, F. Eur. J. Org. Chem. 2007, 4352 and references cited therein.
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MacHetti, F.1
Cecchi, L.2
Trogu, E.3
De Sarlo, F.4
-
50
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78651513225
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Experimental protocols are provided as Supporting Information
-
Experimental protocols are provided as Supporting Information.
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