BishtRef
Articles Journals Publishers Authors Subjects Most Cited New Papers Year Stats Open Access
journal article Jan 01, 2018

Rh-Catalyzed aminative dearomatization of 2-naphthols

Ji-Cheng Yi Hang-Fei Tu Shu-Li You ORCID
Organic & Biomolecular Chemistry Vol. 16 No. 45 pp. 8700-8703 · Royal Society of Chemistry (RSC)
View at Publisher Save 10.1039/c8ob02592d
Abstract
β-Naphthalenones bearing a naked α-amino group could be rapidly constructed through a Rh-catalyzed aminative dearomatization reaction of 2-naphthols with
O
-(2,4-dinitrophenyl)hydroxylamine.
Topics

No keywords indexed for this article. Browse by subject →

References
76
[1]
M. Weber , M.Weber and M.Kleine-Boymann , Phenol in Ullmann's Encyclopedia of Industrial Chemistry , Wiley-VCH , Weinheim , 2004
[2]
S. K. Jackson , K.-L.Wu and T. R. R.Pettus , in Biomimetic Organic Synthesis , Wiley-VCH , Weinheim , 2011 , p. 723 10.1002/9783527634606.ch20
[3]
Roche Angew. Chem., Int. Ed. (2011) 10.1002/anie.201006017
[4]
Quideau Synlett (2008) 10.1055/s-2008-1032094
[5]
Pouységu Tetrahedron (2010) 10.1016/j.tet.2009.12.046
[6]
Ngatimin Aust. J. Chem. (2010) 10.1071/ch09625
[7]
Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives

Weihao Wu, Liming Zhang, Shu-Li You

Chemical Society Reviews 2016 10.1039/c5cs00356c
[8]
Liang Angew. Chem., Int. Ed. (2011) 10.1002/anie.201106127
[9]
Zhuo Angew. Chem., Int. Ed. (2012) 10.1002/anie.201204822
[10]
Transition-Metal-Catalyzed Asymmetric Allylic Dearomatization Reactions

Chun-Xiang Zhuo, Chao Zheng, Shu-Li You

Accounts of Chemical Research 2014 10.1021/ar500167f
[11]
Sun Org. Biomol. Chem. (2016) 10.1039/c5ob02526e
[12]
Zheng Chem (2016) 10.1016/j.chempr.2016.11.005
[13]
Quideau Top. Curr. Chem. (2016) 10.1007/128_2015_665
[14]
R. B. Bedford , in Asymmetric Dearomatization Reactions , ed. S.-L. You , Wiley-VCH, Verlag GmbH & Co. KGaA , 2016 , ch. 10, p. 229 10.1002/9783527698479.ch10
[15]
Wu Acta Chim. Sin. (2017) 10.6023/a17020049
[16]
Dong J. Am. Chem. Soc. (2008) 10.1021/ja711018z
[17]
Dohi Angew. Chem., Int. Ed. (2008) 10.1002/anie.200800464
[18]
Boppisetti Org. Lett. (2009) 10.1021/ol8029092
[19]
Quideau Angew. Chem., Int. Ed. (2009) 10.1002/anie.200901039
[20]
Uyanik Angew. Chem., Int. Ed. (2010) 10.1002/anie.200907352
[21]
Uyanik Tetrahedron (2010) 10.1016/j.tet.2010.04.060
[22]
Oguma J. Am. Chem. Soc. (2012) 10.1021/ja310203c
[23]
Dohi J. Am. Chem. Soc. (2013) 10.1021/ja401074u
[24]
Oguma Chem. Commun. (2014) 10.1039/c4cc01555j
[25]
Dhineshkumar Chem. Commun. (2016) 10.1039/c6cc04894c
[26]
Uyanik ACS Catal. (2017) 10.1021/acscatal.6b03380
[27]
Antien Tetrahedron (2017) 10.1016/j.tet.2017.04.028
[28]
Uyanik Angew. Chem., Int. Ed. (2017) 10.1002/anie.201612463
[29]
Companys Chem. – Eur. J. (2017) 10.1002/chem.201703238
[30]
Dohi J. Org. Chem. (2017) 10.1021/acs.joc.7b02037
[31]
Uyanik J. Org. Chem. (2017) 10.1021/acs.joc.7b01941
[32]
Assal J. Org. Chem. (2017) 10.1021/acs.joc.7b02366
[33]
Deruer J. Org. Chem. (2017) 10.1021/acs.joc.7b01595
[34]
Esguerra Angew. Chem., Int. Ed. (2018) 10.1002/anie.201710271
[35]
Hashimoto Angew. Chem., Int. Ed. (2018) 10.1002/anie.201803889
[36]
Rousseaux J. Am. Chem. Soc. (2011) 10.1021/ja203644q
[37]
Rudolph Angew. Chem., Int. Ed. (2011) 10.1002/anie.201102069
[38]
Nan J. Am. Chem. Soc. (2013) 10.1021/ja410060e
[39]
Nemoto Angew. Chem., Int. Ed. (2013) 10.1002/anie.201209317
[40]
Xu J. Am. Chem. Soc. (2014) 10.1021/ja508645j
[41]
Nemoto Adv. Synth. Catal. (2014) 10.1002/adsc.201400247
[42]
Yang J. Am. Chem. Soc. (2015) 10.1021/jacs.5b01285
[43]
Zheng J. Am. Chem. Soc. (2015) 10.1021/jacs.5b01707
[44]
Yang Angew. Chem., Int. Ed. (2015) 10.1002/anie.201410257
[45]
Enantioselective Palladium‐Catalyzed Dearomative Cyclization for the Efficient Synthesis of Terpenes and Steroids

Kang Du, Pan Guo, Yuan Chen et al.

Angewandte Chemie International Edition 2015 10.1002/anie.201411817
[46]
Yang Angew. Chem., Int. Ed. (2015) 10.1002/anie.201503056
[47]
Cheng Angew. Chem., Int. Ed. (2016) 10.1002/anie.201511519
[48]
Bai Angew. Chem., Int. Ed. (2016) 10.1002/anie.201601570
[49]
Xu Angew. Chem., Int. Ed. (2016) 10.1002/anie.201608724
[50]
Wu Chem. Sci. (2016) 10.1039/c5sc04130a

Showing 50 of 76 references

Metrics
19
Citations
76
References
Details
Published
Jan 01, 2018
Vol/Issue
16(45)
Pages
8700-8703
License
View
Authors
J
Ji-Cheng Yi

State Key Laboratory of Organometallic Chemistry; Shanghai Institute of Organic Chemistry; Center for Excellence in Molecular Synthesis; University of Chinese Academy of Sciences; Chinese Academy of Sciences

H
Hang-Fei Tu

State Key Laboratory of Organometallic Chemistry; Shanghai Institute of Organic Chemistry; Center for Excellence in Molecular Synthesis; University of Chinese Academy of Sciences; Chinese Academy of Sciences

S
Shu-Li You

State Key Laboratory of Organometallic Chemistry; Shanghai Institute of Organic Chemistry; Center for Excellence in Molecular Synthesis; University of Chinese Academy of Sciences; Chinese Academy of Sciences

Funding
National Natural Science Foundation of China Award: 21332009
Chinese Academy of Sciences Award: XDB20000000
Ministry of Science and Technology of the People's Republic of China Award: 2016YFA0202900
Cite This Article
Ji-Cheng Yi, Hang-Fei Tu, Shu-Li You (2018). Rh-Catalyzed aminative dearomatization of 2-naphthols. Organic & Biomolecular Chemistry, 16(45), 8700-8703. https://doi.org/10.1039/c8ob02592d
Related

You May Also Like

Analysis of the reactions used for the preparation of drug candidate molecules

John S. Carey, David Laffan · 2006

1,808 citations

The activation strain model of chemical reactivity

Willem-Jan van Zeist, F. Matthias Bickelhaupt · 2010

678 citations

Far-red and near infrared BODIPY dyes: synthesis and applications for fluorescent pH probes and bio-imaging

Yong Ni, Jishan Wu · 2014

638 citations

Solution-state 2D NMR of ball-milled plant cell wall gels in DMSO-d6/pyridine-d5

Hoon Kim, John Ralph · 2010

604 citations

HIV-1 protease: mechanism and drug discovery

Ashraf Brik, Chi-Huey Wong · 2002

380 citations