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4
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56749129716
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For reviews on the use of TEMPO in synthesis, see: a
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For reviews on the use of TEMPO in synthesis, see: a) T. Vogler, A. Studer, Synthesis 2008, 2163;
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(2008)
Synthesis
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Vogler, T.1
Studer, A.2
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8
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38349133722
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for the use of TEMPO as an oxidant in rhodium-catalyzed C-H arylation reactions, see: e T. Vogler, A. Studer, Org. Lett. 2008, 10, 129.
-
for the use of TEMPO as an oxidant in rhodium-catalyzed C-H arylation reactions, see: e) T. Vogler, A. Studer, Org. Lett. 2008, 10, 129.
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-
-
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10
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0035498332
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for a review, see
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for a review, see: C. Ollivier, P. Renaud, Chem. Rev. 2001, 101, 3415.
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Ollivier, C.1
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J. Hassan, M. Sévignon, C. Cozzi, E. Schulz, M. Lemaire, Chem. Rev. 2002, 102, 1359.
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A. Krasovskiy, A. Tishkov, V. del Amo, H. Mayr, P. Knochel, Angew. Chem. 2006, 118, 5132;
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14
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15044349486
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For the coupling of alkynyl metal compounds with dinitrogen tetroxide, see
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For the coupling of alkynyl metal compounds with dinitrogen tetroxide, see: C. J. Woltermann, H. Shechter, Helv. Chim. Acta 2005, 88, 354.
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a) P. Knochel, W. Dohle, N. Gommermann, F. F. Kneisel, F. Kopp, T. Korn, I. Sapountzis, V. A. Vu, Angew. Chem. 2003, 115, 4438;
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9444224983
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b) H. Ren, A. Krasovskiy, P. Knochel, Org. Lett. 2004, 6, 4215.
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G. Cahiez, A. Moyeux, J. Buendia, C. Duplais, J. Am. Chem. Soc. 2007, 129, 13788.
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19
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56749142420
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2) prior to the renewed addition of PhMgBr. (The product was obtained in the same yield with or without this extra step.)
-
2) prior to the renewed addition of PhMgBr. (The product was obtained in the same yield with or without this extra step.)
-
-
-
-
20
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-
56749092634
-
-
The following amounts of PhMgBr were added: 13 mol% in the third and fourth cycles, 12 mol% in the fifth and sixth cycles, and 11 mol% in the seventh and eighth cycles.
-
The following amounts of PhMgBr were added: 13 mol% in the third and fourth cycles, 12 mol% in the fifth and sixth cycles, and 11 mol% in the seventh and eighth cycles.
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-
-
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21
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54749090939
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For transition-metal-catalyzed aerobic oxidations, see
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For transition-metal-catalyzed aerobic oxidations, see: J. Piera, J.-E. Bäckvall, Angew. Chem. 2008, 120, 3558;
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Angew. Chem
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0026539112
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a) B. H. Lipshutz, K. Siegmann, E. Garcia, Tetrahedron 1992, 48, 2579;
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Lipshutz, B.H.1
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25
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0037016994
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c) C. M. P. Kronenburg, C. H. M. Amijs, P. Wijkens, J. T. B. Jastrzebski, G. van Koten, Tetrahedron Lett. 2002, 43, 1113.
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Kronenburg, C.M.P.1
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Jastrzebski, J.T.B.4
van Koten, G.5
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