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58
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0021919844
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For bis[bis(trimethylsilyl)amido] tin(II), see: Wang, W.-B.; Roskamp, E. J. J. Org. Chem. 1992, 57, 6101-6103.
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60
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0002541033
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Evans, D.A.1
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For sodium diethyldihydroaluminate, see: Sim, T. B.; Yoon, N. M. Synlett 1994, 10, 827-828.
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Yang, K.-W.1
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For methyl magnesium iodide, see
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For methyl magnesium iodide, see: Houghton, R. P.; Williams, C. S. Tetrahedron Lett. 1967, 8, 3929-3931.
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Houghton, R.P.1
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For sodium hydride, see: Singh, B. Tetrahedron Lett. 1971, 12, 321-322.
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Singh, B.1
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68
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Levi, E.M.1
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For other miscellaneous methods, see: (a) Silicon tetrachloride. Chan, H.; Wong, L. T. L. J. Org. Chem. 1969, 34, 2766-2767.
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For other miscellaneous methods, see: (a) Silicon tetrachloride. Chan, H.; Wong, L. T. L. J. Org. Chem. 1969, 34, 2766-2767.
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70
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Sodium cyanide. Hogberg, T.; Strom, P.; Ebner, M.; Ramsby, S. J. Org. Chem. 1987, 52, 2033-2036.
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(b) Sodium cyanide. Hogberg, T.; Strom, P.; Ebner, M.; Ramsby, S. J. Org. Chem. 1987, 52, 2033-2036.
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71
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Enzymes. West, J. B.; Wong, C.-H. Tetrahedron Lett. 1987, 28, 1629-1632.
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(c) Enzymes. West, J. B.; Wong, C.-H. Tetrahedron Lett. 1987, 28, 1629-1632.
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72
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Electrochemical method. Arai, K.; Shaw, C. H.; Nozawa, K.; Kawai, K.; Nakajima, S. Tetrahedron Lett. 1987, 28, 441-442.
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(d) Electrochemical method. Arai, K.; Shaw, C. H.; Nozawa, K.; Kawai, K.; Nakajima, S. Tetrahedron Lett. 1987, 28, 441-442.
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73
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For examples of aminolysis of methyl esters, see: (a) Labelle, M.; Gravel, D. Chem. Commun. 1985, 105-106.
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(c) Chou, W.-C.; Tan, C.-W.; Chen, S.-F.; Ku, H. J. Org. Chem. 1998, 63, 10015-10017.
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31344471493
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We choose p-nitrobenzo ester rather than other substituted benzoates because the rate of aminolysis of the substituted benzoates increases as the substituents change from a strong electron-donating group to a strong electron-withdrawing group, see: Um, I.-H, Jeon, S.-E, Seok, J.-A. Chem.-Eur. J. 2006, 12, 1237-1243
-
We choose p-nitrobenzo ester rather than other substituted benzoates because the rate of aminolysis of the substituted benzoates increases as the substituents change from a strong electron-donating group to a strong electron-withdrawing group, see: Um, I.-H.; Jeon, S.-E.; Seok, J.-A. Chem.-Eur. J. 2006, 12, 1237-1243.
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For recents reviews, see: a
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For recents reviews, see: (a) De La Hoz, A.; Diaz-Ortiz, A.; Moreno, A. Chem. Soc. Rev. 2005, 34, 164-178.
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(41 ) For tert-butoxide-mediated aminolysis, see: (a) Varma, R. S.; Naicker, K. P. S Tetrahedron Lett. 1999, 40, 6177-6180.
-
(41 ) For tert-butoxide-mediated aminolysis, see: (a) Varma, R. S.; Naicker, K. P. S Tetrahedron Lett. 1999, 40, 6177-6180.
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(b) Zradni, F.-Z.; Hamelin, J.; Derdour, A. Synth. Commun. 2002, 32, 3525-3531.
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Zradni, F.-Z.1
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85
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0037450952
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For aminolysis in the absence of base or induced by tenbutoxide, see
-
For aminolysis in the absence of base or induced by tenbutoxide, see: Perreux, L.; Loupy, A.; Delmotte, M. Tetrahedron 2003, 59, 2185-2189.
-
(2003)
Tetrahedron
, vol.59
, pp. 2185-2189
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Perreux, L.1
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Delmotte, M.3
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86
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34249932029
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-
For technical reasons (minimum filling of the reaction vessel = 0.5 mL), it was not feasible to run those reactions under solvent-free conditions.
-
For technical reasons (minimum filling volume of the reaction vessel = 0.5 mL), it was not feasible to run those reactions under solvent-free conditions.
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