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. Author manuscript; available in PMC: 2013 Jan 1.
Published in final edited form as: Synlett. 2012 Jan;2012(1):54–56. doi: 10.1055/s-0031-1289567

Table 2.

Reaction scope of homodimerizationa

graphic file with name nihms394026t2.jpg
entry R 4 yield (4)b 4/5c
1 n-decyl 4b 72% 14/1
2 cyclohexyl 4c 69% 13/1
3d cyclopentyl 4d 85% 25/1
4d graphic file with name nihms394026t3.jpg 4e 61% 12/1
5 PhCH2CH2 4f 61% 11/1
6 graphic file with name nihms394026t4.jpg 4g 78% 10/1
7 graphic file with name nihms394026t5.jpg 4h 81% 11/1
8 Ph 4i 8% 12/1
9 2-propenyl 4j - -
a

Reaction run in Schlenk tubes under nitrogen; [alkyne] = 0.1 M.

b

Isolated yield and containing small amount of inseparable 5.

c

Determined by crude 1H NMR.

d

Reaction time: 48 h; catalyst loading: 10 mol %.