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. Author manuscript; available in PMC: 2013 Feb 7.
Published in final edited form as: Org Lett. 2010 Feb 19;12(4):808–811. doi: 10.1021/ol902833p

Table 1.

Reactions of 2-(Phenylsulfonyl)-1,3-oxazole 1

graphic file with name nihms171983u2.jpg
entry electrophile producta,b yieldc (%)
1 graphic file with name nihms171983t1.jpg graphic file with name nihms171983t2.jpg 6 87
2 graphic file with name nihms171983t3.jpg graphic file with name nihms171983t4.jpg 7 81
3 n-Bu3SnCl graphic file with name nihms171983t5.jpg 8 86
4 CH3I graphic file with name nihms171983t6.jpg 9 91
5 graphic file with name nihms171983t7.jpg graphic file with name nihms171983t8.jpg 10 72
6 graphic file with name nihms171983t9.jpg graphic file with name nihms171983t10.jpg 11 75
7 graphic file with name nihms171983t11.jpg graphic file with name nihms171983t12.jpg 12 87
8 graphic file with name nihms171983t13.jpg graphic file with name nihms171983t14.jpg 13 81
a

Reaction conditions: A THF solution of sulfone 1 (1.0 equiv; 2.0 mmol) was added into a solution of LDA (1.1 equiv) in THF at −78 °C. After stirring under N2 for 1 h, electrophile in THF solution was added with subsequent warming to 22 °C.

b

Products were purified by flash silica gel chromatography.

c

Yields are reported for isolated and purified product.