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. 2019 Apr 28;24(9):1671. doi: 10.3390/molecules24091671

Table 2.

Decarbonylative stannylation of acyl fluorides a,b.

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3a, 90%
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3b, 81%
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3c, 63%
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3d, 67%
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3e, 82%
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3f, 56%
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3g, 85%
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3h, 64%
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3i, 61%
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3j, 50%
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3k, 87%
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3l, 61%
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3m, 86%
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3n, 72%
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3o, 90%
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3p, 51%
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3q, 79%
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3r, 82%
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3s, 62%
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3t, 84%

aReaction conditions: 1 (0.2 mmol), 2 (0.24 mmol), NiCl2 (0.01 mmol), CsF (0.4 mmol), toluene (1 mL), 140 °C, 24 h. b Isolated yields.