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53949095967
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V. Jäger, P. A. Colinas in ref. 1 a. Chapter 6:
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b) V. Jäger, P. A. Colinas in ref. 1 a). Chapter 6:
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7
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53949120970
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P. Caramella, P. Grünanger, in ref. 1 b, Chapter 3.
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e) P. Caramella, P. Grünanger, in ref. 1 b), Chapter 3.
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9
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4544225097
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For selected recent applications of phenylisocyanate see: a
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For selected recent applications of phenylisocyanate see: a) K. N. Fleming, R. E. Taylor, Angew. Chem. 2004, 116, 1760-1762;
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Angew. Chem
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Koroleva, E.V.1
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33645375911
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Zh. Org. Khim. 2006, 42, 246-253;
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g) A. Kadowaki, Y. Nagata, H. Unob, A. Kamimura, Tetrahedron Lett. 2007, 48, 1823-1825;
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h) E. V. Koroleva, Y. M. Katok, F. A. Lakhvich, Natsyyanal'nai Akademii Navuk Belarusi, Seryya Khimichnykh Navuk 2000, 3, 70-74;
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Chem. Abstr. 2000, 134, 131337;
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i) J. Siu, I. R. Baxendale, R. A. Lewthwaite, S. V. Ley, Org. Biomol. Chem. 2005, 3, 3140-3160;
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0028027621
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Tolylene 2,4-diisocyanate: M. G. Leslie-Smith, R. M. Paton, N. Webb. Tetrahedron Lett. 1994, 35, 9251-9254.
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Tolylene 2,4-diisocyanate: M. G. Leslie-Smith, R. M. Paton, N. Webb. Tetrahedron Lett. 1994, 35, 9251-9254.
-
-
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24
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-
0000720870
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1,4-Phenylene diisocyanate: V. Jäger, I. Müller, Tetrahedron 1985, 41, 3519-3528.
-
1,4-Phenylene diisocyanate: V. Jäger, I. Müller, Tetrahedron 1985, 41, 3519-3528.
-
-
-
-
25
-
-
0036331047
-
-
For recent selected examples that use 1,4-phenylene diisocyanate see: a
-
For recent selected examples that use 1,4-phenylene diisocyanate see: a) M. Lemaire, N. Veny, T. Gefflaut, E. Gallienne, R. Chênevert, J. Bolte, Synlett 2002, 1359-1361;
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Lemaire, M.1
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27
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0019976078
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4-Chlorophenyl isocyanate: A. P. Kozikowski, P. D. Stein, J. Am. Chem. Soc. 1982, 104, 4023-4024.
-
4-Chlorophenyl isocyanate: A. P. Kozikowski, P. D. Stein, J. Am. Chem. Soc. 1982, 104, 4023-4024.
-
-
-
-
28
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-
33751273452
-
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For selected recent applications of 4-chlorophenyl isocyanate see: a
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For selected recent applications of 4-chlorophenyl isocyanate see: a) W. Itano, T. Ohshima, M. Shibasaki, Synlett 2006, 3053-3056;
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c) S. Ghorai, R. Mukhopadhyay, A. P. Kundu, A. Bhattacharjya, Tetrahedron 2005, 61, 2999-3012;
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Acetyl chloride: a) E. Kaji, K. Harada, S. Zen, Chem. Pharm. Bull. 1978, 26, 3254-3256;
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Ethyl chloroformate/triethylamine and benzenesulphonyl chloride/triethylamine: T. Shimizu, Y. Hayashi, H. Shibafuchi, K. Teramura, Bull. Chem. Soc. Jpn. 1986, 59, 2827-2831.
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-
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-
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40
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0009184053
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For selected applications of p-toluensulphonyl chloride see: a
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For selected applications of p-toluensulphonyl chloride see: a) S. Kwiatkowski, M. Langwald, Monatsh. Chem. 1986, 117, 1091-1093;
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Acetic anhydride/sodium acetate: A. Mckillop, R. J. Kobylecki. Tetrahedron 1974, 30, 1365-1371:
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Acetic anhydride/sodium acetate: A. Mckillop, R. J. Kobylecki. Tetrahedron 1974, 30, 1365-1371:
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47
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0030977541
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Di fert-butyldicarbonate/4-dimethylaminopyridine: a) Y. Basel, A. Hassner, Synthesis 1997, 309-312:
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48
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0036330960
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for recent selected examples see: b
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For other dehydrating agents see: a N,N-dielhylaminosulfur trifluoride (DAST) and Methyl N-(triethylammoniosulphonyl)carbamate (Burgess salt): N. Maugein, A. Wagner, C. Mioskowsi, Tetrahedron Lett. 1997, 38, 1547-1550;
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For other dehydrating agents see: a) N,N-dielhylaminosulfur trifluoride (DAST) and Methyl N-(triethylammoniosulphonyl)carbamate (Burgess salt): N. Maugein, A. Wagner, C. Mioskowsi, Tetrahedron Lett. 1997, 38, 1547-1550;
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53
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p-toluensulphonic acid: T. Shimizu, Y. Hayashi, K. Teramura, Bull. Chem. Soc. Jpn. 1984, 57, 2531-2534;
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54
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0038045344
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4-(4,6-dimelhoxy[1,3,5]triazin-2-yl)-4-melhylmorpholinium chloride (DMTMM) G. Giacomelli, L. De Luca, A. Porcheddu, Tetrahedron, 2003, 59, 5437-5440;
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c) 4-(4,6-dimelhoxy[1,3,5]triazin-2-yl)-4-melhylmorpholinium chloride (DMTMM) G. Giacomelli, L. De Luca, A. Porcheddu, Tetrahedron, 2003, 59, 5437-5440;
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55
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53949097694
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58
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33750861083
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61
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For recent examples see: a) T. Gefflaut, C. Martin, S. Delor, P. Besse, H. Veschambre, J. Bolte, J. Org. Chem. 2001, 66, 2296-2301;
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A complete study of the mechanism will be reported in due course
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A complete study of the mechanism will be reported in due course.
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89
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11844255741
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For selected processes utilising copper metal as catalyst/reagent source see: 1,3-dipolar cycloadditions of azides and alkynes (Huisgen reaction): a) F. Himo, T. Lovell, R. Hilgraf, V. V. Rostovtsev, L. Noodleman, K. B. Shatpless, V. V. Fokin, J. Am. Chem. Soc. 2005, 127, 210-216;
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For selected processes utilising copper metal as catalyst/reagent source see: 1,3-dipolar cycloadditions of azides and alkynes (Huisgen reaction): a) F. Himo, T. Lovell, R. Hilgraf, V. V. Rostovtsev, L. Noodleman, K. B. Shatpless, V. V. Fokin, J. Am. Chem. Soc. 2005, 127, 210-216;
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coupling of aryl halides (Ullmann-Jourdan reaction): c) W. Boomgaarden, F. Vogtle, M. Nieger, H. Hupfer, Chem. Eur. J. 1999, 5, 345-355;
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d) R. Csuk, A. Barlhel, C. Raschke, Tetrahedron 2004, 60, 5737-5750; coupling of aryl halides and alkyl halides
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e) J. K. Park, H. G. Lee, C. Bolm, B. M. Kim, Chem. Eur. J. 2005, 11, 945-950; decarboxylation:
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Angew. Chem. Int. Ed. 2005, 44, 3297-3301. Allylic amination of olefins:
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100
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53949093830
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See reference [2d], Chapter 1, p. 45.
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See reference [2d], Chapter 1, p. 45.
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101
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Angew. Chem. Int. Ed. 2005, 44, 4036-4038.
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