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119Sn chemical shifts are in good agreement with those reported in solution for organotin reagents with similar functionalities. See: (a) Smith, P. J.; Tupciauskas, A. P. Annu. Rep. NMR Spectrosc. 1978, 8, 291-370. (b) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1985, 16, 73-186. (c) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1999, 38, 203-264.
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55
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1542693412
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119Sn chemical shifts are in good agreement with those reported in solution for organotin reagents with similar functionalities. See: (a) Smith, P. J.; Tupciauskas, A. P. Annu. Rep. NMR Spectrosc. 1978, 8, 291-370. (b) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1985, 16, 73-186. (c) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1999, 38, 203-264.
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119Sn chemical shifts are in good agreement with those reported in solution for organotin reagents with similar functionalities. See: (a) Smith, P. J.; Tupciauskas, A. P. Annu. Rep. NMR Spectrosc. 1978, 8, 291-370. (b) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1985, 16, 73-186. (c) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1999, 38, 203-264.
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note
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In liquid phase, organolithium amides are known to be trapped by triorganotin halides to afford the corresponding N-stannylated amines. Because of the high sensitivity of this type of reagent to moisture, MAS NMR characterization of 6a-i was not attempted.
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