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. Author manuscript; available in PMC: 2011 Mar 3.
Published in final edited form as: Organometallics. 2010 Mar 3;29(7):1661–1669. doi: 10.1021/om901042j

Table 3.

Pd(0)-Catalyzed Carbon–Carbon Bond Insertion with 3c to Yield Si–C(sp2) Bond Cleavage Products

graphic file with name nihms-184733-t0024.jpg
entry substrate product % yielda
1 graphic file with name nihms-184733-t0025.jpg graphic file with name nihms-184733-t0026.jpg 77(20)
2 graphic file with name nihms-184733-t0027.jpg graphic file with name nihms-184733-t0028.jpg 76(14)
3 graphic file with name nihms-184733-t0029.jpg graphic file with name nihms-184733-t0030.jpg 66(10)
4 graphic file with name nihms-184733-t0031.jpg graphic file with name nihms-184733-t0032.jpg 66(25)b
a

As determined by 1H NMR spectroscopic analysis relative to an internal standard (PhSiMe3). Isolated yields are shown in parentheses.

b

Hydrolysis gave (α,β-unsaturated aldehyde 4h′ when subjected to chromatography.

graphic file with name nihms-184733-t0033.jpg