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. Author manuscript; available in PMC: 2013 Aug 29.
Published in final edited form as: J Am Chem Soc. 2012 Aug 20;134(34):14232–14237. doi: 10.1021/ja306323x

Table 3.

Palladium-Catalyzed Elimination Reactions of Alkyl Sulfonates

graphic file with name nihms-402431-f0025.jpg
entry substrate temperature (°C), x yield a
1 graphic file with name nihms-402431-t0026.jpg 80, 6 98 [18:1]
2 graphic file with name nihms-402431-t0027.jpg 90, 6 97
3 graphic file with name nihms-402431-t0028.jpg 100, 17 96
4 graphic file with name nihms-402431-t0029.jpg 100, 25 94 [1:2]
5 graphic file with name nihms-402431-t0030.jpg 80, 12 90 [14:1]
a

The isolated yield (%) is provided (average of two experiments). For eliminations in which >2% of the internal olefin is generated, the ratio of terminal:internal olefins (determined via 1H NMR spectroscopy) is given in brackets.