6
17
Synlett
S. K. Chittimalla et al.
Letter
plication of the procedures is exemplified by synthesizing
biphenyl natural products aucuparin and 2′-hydroxy-3,4,5-
trimethoxybiphenyl. Further investigations to broaden the
scope of this methodology to incorporate heteroaryl boron-
ic acids and arylboronic acids bearing electron-withdraw-
ing groups into the present domino reaction are in prog-
ress.
Soc. 2005, 127, 17978. (d) Ackermann, L.; Althammer, A. Org.
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Acknowledgment
(8) (a) Chittimalla, S. K.; Bandi, C.; Putturu, S.; Kuppusamy, R.;
Boellaard, K. C.; Tan, D. C. T.; Lum, D. M. J. Eur. J. Org. Chem. 2014,
The authors sincerely thank Dr. Takeshi Yura and Dr. Anjan
Chakrabarti for encouragement.
2565. (b) Chittimalla, S. K.; Kuppusamy, R.; Bandi, C. Synlett
2014, 25, 1991.
(9) (a) Parumala, S. K. R.; Peddinti, R. K. Org. Lett. 2013, 15, 3546.
(
b) Dohi, T.; Washimi, N.; Kamitanaka, T.; Fukushima, K.; Kita, Y.
Supporting Information
Angew. Chem. Int. Ed. 2011, 50, 6142. (c) Dohi, T.; Kamitanaka,
T.; Watanabe, S.; Hu, Y.; Washimi, N.; Kita, Y. Chem. Eur. J. 2012,
1
Supporting information for this article is available online at
http://dx.doi.org/10.1055/s-0034-1379987.
8, 13614.
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10) (a) Kharasch, M. S.; Tawney, P. O. J. Am. Chem. Soc. 1941, 63,
2
2
308. (b) Rodríguez, C.; Vázquez, Á.; Nudelman, N. S. ARKIVOC
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©
Georg Thieme Verlag Stuttgart · New York — Synlett 2015, 26, 613–618