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. Author manuscript; available in PMC: 2011 Sep 29.
Published in final edited form as: J Am Chem Soc. 2010 Sep 29;132(38):13179–13181. doi: 10.1021/ja1061196

Table 2.

Alcohol Addition Scope

graphic file with name nihms233585t2.jpg
entry R product yield(%)b
1 Bn 2 89
2 Me 3 79
3 allyl 4 78
4 propargyl 5 85
5 4-MeO-C6H4CH2OH 6 81
6 graphic file with name nihms233585t3.jpg 7 80
7 graphic file with name nihms233585t4.jpg 8 75
8c graphic file with name nihms233585t5.jpg 9 81d
9 graphic file with name nihms233585t6.jpg 10 75d
10 graphic file with name nihms233585t7.jpg 11 89
a

See Supporting Information for details.

b

Isolated yields.

c

CH2Cl2 used as solvent.

d

1.2:1 dr (determined by 1H NMR spectroscopy).