Organic Letters
Letter
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ASSOCIATED CONTENT
Supporting Information
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*
S
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810. (d) Okamoto, K.; Sakata, N.; Ohe, K. Org. Lett. 2015, 17, 4670.
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9) Aryl(cyano)iodonium triflate has recently been applied to
Experimental procedures and characterization data for all
1
13
(
(
electrophilic cyanation reactions. See: (a) Shu, Z.; Ji, W.; Wang, X.;
Zhou, Y.; Zhang, Y.; Wang, J. Angew. Chem., Int. Ed. 2014, 53, 2186.
(b) Zhu, D.; Chang, D.; Shi, L. Chem. Commun. 2015, 51, 7180.
AUTHOR INFORMATION
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(
c) Wang, X.; Studer, A. J. Am. Chem. Soc. 2016, 138, 2977.
(10) Zhdankin, V. V.; Kuehl, C. J.; Krasutsky, A. P.; Bolz, J. T.;
*
Mismash, B.; Woodward, J. K.; Simonsen, A. J. Tetrahedron Lett. 1995,
36, 7975.
*
(
2
(
11) Frei, R.; Courant, T.; Wodrich, M. D.; Waser, J. Chem. - Eur. J.
015, 21, 2662.
12) (a) Wang, Y.-F.; Qiu, J.; Kong, D.; Gao, Y.; Lu, F.; Karmaker, P.
G.; Chen, F.-X. Org. Biomol. Chem. 2015, 13, 365. (b) Chowdhury, R.;
Schorgenhumer, J.; Novacek, J.; Waser, M. Tetrahedron Lett. 2015, 56,
911. (c) Chen, M.; Huang, Z.-T.; Zheng, Q.-Y. Org. Biomol. Chem.
015, 13, 8812. (d) Ma, B.; Lin, X.; Lin, L.; Feng, X.; Liu, X. J. Org.
ORCID
Notes
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2
The authors declare no competing financial interest.
Chem. 2017, 82, 701.
ACKNOWLEDGMENTS
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(13) (a) Le Vaillant, F.; Wodrich, M. D.; Waser, J. Chem. Sci. 2017, 8,
1790. (b) Zhou, Q.-Q.; Liu, D.; Xiao, W.-J.; Lu, L.-Q. Huaxue Xuebao
2017, 75, 110.
This work was supported by JSPS KAKENHI Grant Number
JP16K17868 and a grant from Meiji Seika Pharma Co., Ltd.
Award in Synthetic Organic Chemistry, Japan.
(
14) Shen, H.; Li, J.; Liu, Q.; Pan, J.; Huang, R.; Xiong, Y. J. Org.
Chem. 2015, 80, 7212.
15) For reactions via Lewis acidic activation of hypervalent iodine
(
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(
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(
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(
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̈
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(
3
2
2
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−1
13
shifted from 2137 to 2162 cm . In addition, in the C NMR
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(
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3
(
(
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4
(
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(
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̃
8
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(
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D
Org. Lett. XXXX, XXX, XXX−XXX