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. Author manuscript; available in PMC: 2008 Aug 26.
Published in final edited form as: Chem Rev. 2007 May 27;107(6):2503–2545. doi: 10.1021/cr0509556

Table 31.

Diethylzinc additions to ketones under solvent-free, highly concentrated, and standard conditions.

graphic file with name nihms-63649-t0083.jpg
solvent-free or highly concentrated conditions
standard conditions
entry substrates L* (moi%) t (h) y (%) ee (%) L*(mol%) t (h) y (%) ee (%) (config.)
graphic file with name nihms-63649-t0084.jpg
1 X = H 1
0.5
4
21
75
78
97a
96a
2 29 71 96 (S)
2 X = 3-CF3 0.5 17 77 96a 2 14 56 98
3 X = 4-OMe 1
1
12
15
50
72
81a
89b
10 111 85 94
4 graphic file with name nihms-63649-t0085.jpg 0.5
0.5
12
24
74
76
98a
98b
2 27 90 97
5 graphic file with name nihms-63649-t0086.jpg 1
1
24
24
78
85
80a
80b
2 102 79 88 (R)
6 graphic file with name nihms-63649-t0087.jpg 1 15 71 90b 2 26 80 90
7 graphic file with name nihms-63649-t0088.jpg 1 22 53 93b 2 46 56 96
8 graphic file with name nihms-63649-t0089.jpg 1 22 36 96b 10 40 76 98
a

Solvent-free conditions.

b

2 Equiv toluene was added to the reaction.