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. Author manuscript; available in PMC: 2009 Apr 1.
Published in final edited form as: Bioorg Chem. 2008 Feb 11;36(2):96–104. doi: 10.1016/j.bioorg.2007.12.003

Table 1.

Yields and conditions of Wittig reaction.

Aldehyde Phosphonium salt Product (yield, %)
2a graphic file with name nihms43408t1.jpg(3a) HYG (5)[a]
2a 4-(TBSO)C6H4CH2PPh3Br (3b) YYG (23)[a]
2a BnPPh3Br (3c) FYG (53)[b]
2a H2NCOCH2PPh3Br (3d) NYG (49)[b]
2a graphic file with name nihms43408t2.jpg(3e) WYG (18)[b,c]
2b 4-(TBSO)C6H4CH2PPh3Br (3b) YWG (42)[b]
2b BnPPh3Br (3c) FWG (44)[b]
[a]

2M aqueous NaOH / CH2Cl2.

[b]

t-BuOK / t-BuOH.

[c]

After Boc cleavage (see Experimental Section).