3
Table 3. Substrate scope of arylboronic acids
Acknowledgments
We thank the Instrumental Analysis Laboratory, University of
Toyama and Doshisha University for the HRMS measurements
and acknowledge Mrs. A. Sato at A Rabbit Science Co., Ltd. for
elemental analysis. This work was supported by the Sasakawa
Scientific Research Grant from The Japan Science Society.
Entry
1
Arylboronic acid 3
Product 4
Yield (%)a
82
References and notes
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8
9
79
75
10
11
88
45b
12
13
56c
71
OH
OMe
4m
O
O
14
37b,d
a
Isolated yield.
b The reactions using 1.0 mmol arylboronic acid were carried out at 120 °C.
c The reactions using 1.0 mmol arylboronic acid were carried out at 100 °C
d 1.0mmol of 3o was used.