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. Author manuscript; available in PMC: 2011 Nov 15.
Published in final edited form as: Angew Chem Int Ed Engl. 2010 Nov 15;49(47):8930–8933. doi: 10.1002/anie.201003470

Table 1.

Substrate scope for three-component coupling.

graphic file with name nihms257796t1.jpg

Product[a] R Yield [%]
8a Ph 72[b]
8b 4-Cl-C6H4 70[b]
8c 2-thienyl 65[b]
8d 2-furyl 64[b]
8e (E)-CH=CH-C6H5 66[b]
8 f H 57[c]
8g n-pentyl 58[b]
8h iPr 53[c]
8i tBu 36[c]
[a]

Reagents: Silyl glyoxylate (1.5 equiv), nitroalkene (1 equiv), CH2= CHMgBr (1.5 equiv), [4]0=0.1m in C7H8;

[b]

Yield of isolated product.

[c]

Yields were determined by 1H NMR spectroscopy of crude product compared to an internal standard of mesitylene.