Nickel-Catalyzed Reductive Coupling of Aryl Halides with Secondary Alkyl Bromides and Allylic Acetate

Shulin Wang; Qun Qian; Hegui Gong

doi:10.1021/ol3013342

journal article Jun 14, 2012

Nickel-Catalyzed Reductive Coupling of Aryl Halides with Secondary Alkyl Bromides and Allylic Acetate

Shulin Wang Qun Qian Hegui Gong

Organic Letters Vol. 14 No. 13 pp. 3352-3355 · American Chemical Society (ACS)

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References

33

[1]

Rudolph A. Angew. Chem., Int. Ed. (2009) 10.1002/anie.200803611

[2]

Frisch A. C. Angew. Chem., Int. Ed. (2005) 10.1002/anie.200461432

[3]

Hu X. Chem. Sci. (2011) 10.1039/c1sc00368b

[4]

Powell D. A. J. Am. Chem. Soc. (2005) 10.1021/ja0436300

[5]

Lou S. J. Am. Chem. Soc. (2010) 10.1021/ja909689t

[6]

Strotman N. A. Angew. Chem., Int. Ed. (2007) 10.1002/anie.200700440

[7]

Zhou J. J. Am. Chem. Soc. (2004) 10.1021/ja039889k

[8]

Oelke A. J. J. Am. Chem. Soc. (2012) 10.1021/ja300031w

[9]

Gong H. J. Am. Chem. Soc. (2008) 10.1021/ja8041564

[10]

Vechorkin O. J. Am. Chem. Soc. (2009) 10.1021/ja9027378

[11]

Smith S. C. Angew. Chem., Int. Ed. (2008) 10.1002/anie.200802784

[12]

Han C. J. Am. Chem. Soc. (2009) 10.1021/ja902046m

[13]

Thaler T. Nature Chem. (2010) 10.1038/nchem.505

[14]

Joshi-Pangu A. Org. Lett. (2011) 10.1021/ol200098d

[15]

Jana R. Chem. Rev. (2011) 10.1021/cr100327p

[16]

Breitenfeld J. Organometallics (2010) 10.1021/om1007506

[17]

Krasovskiy A. J. Am. Chem. Soc. (2009) 10.1021/ja906803t

[18]

Czaplik W. M. Angew. Chem., Int. Ed. (2009) 10.1002/anie.200804434

[19]

Amatore M. Chem. Commun. (2008) 10.1039/b809626k

[20]

Duplais C. Chem. Commun. (2010) 10.1039/b922280d

[21]

Czaplik W. M. Synlett (2009)

[22]

Amatore M. Chem.–Eur. J. (2010) 10.1002/chem.201000178

[23]

Durandetti M. J. Org. Chem. (1996) 10.1021/jo9518314

[24]

Everson D. A. J. Am. Chem. Soc. (2010) 10.1021/ja9093956

[25]

Yan C.-S. Chem.—Eur. J. (2012) 10.1002/chem.201200190

[26]

Everson D. A. J. Am. Chem. Soc. (2012) 10.1021/ja301769r

[27]

Yu X. Org. Lett. (2011) 10.1021/ol200617f

[28]

Dai Y. Chem.—Eur. J. (2012) 10.1002/chem.201102984

[29]

Wu F. Org. Lett. (2012) 10.1021/ol3011198

[30]

10.1039/c2cc33232a

[31]

Qian X. Angew. Chem., Int. Ed. (2011) 10.1002/anie.201104390

[32]

Gomes P. Org. Lett. (2003) 10.1021/ol0340641

[33]

Mayer M. Adv. Synth. Catal. (2010) 10.1002/adsc.201000228

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Details

Published: Jun 14, 2012
Vol/Issue: 14(13)
Pages: 3352-3355

Authors

S

Shulin Wang

Department of Chemistry, Shanghai University, 99 Shang-Da Road, Shanghai 200444, China

Q

Qun Qian

Department of Chemistry, Shanghai University, 99 Shang-Da Road, Shanghai 200444, China

H

Hegui Gong

Department of Chemistry, Shanghai University, 99 Shang-Da Road, Shanghai 200444, China

Cite This Article

Shulin Wang, Qun Qian, Hegui Gong (2012). Nickel-Catalyzed Reductive Coupling of Aryl Halides with Secondary Alkyl Bromides and Allylic Acetate. Organic Letters, 14(13), 3352-3355. https://doi.org/10.1021/ol3013342

Nickel-Catalyzed Reductive Coupling of Aryl Halides with Secondary Alkyl Bromides and Allylic Acetate

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