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- C8–H bond activation vs. C2–H bond activation: from naphthyl amines to lactams. Renyi Shi, Lijun Lu, Hangyu Xie, Jingwen Yan, Ting Xu, Hua Zhang, Xiaotian Qi, Yu Lan, Aiwen Lei
, Chem. Commun.
, 2016
, 52
, 13307
- Metalated covalent organic frameworks: from synthetic strategies to diverse applications. Qun Guan, Le-Le Zhou, Yu-Bin Dong
, Chem. Soc. Rev.
, 2022
, 51
, 6307
- An IR, NMR, dipole moment and X-ray study on intramolecular O–H ⋯ N hydrogen bonding in 8-hydroxy-N,N-dimethyl-1-naphthylamine. E. Grech, J. Nowicka-Scheibe, Z. Olejnik, T. Lis, Z. Pawełka, Z. Malarski, L. Sobczyk
, J. Chem. Soc., Perkin Trans. 2
, 1996
, 343
- Photo/electrocatalytic site-selective C–H functionalization of 8-aminoquinolines and their analogues. Huijie Qiao, Kun Zhao, Yuwei Li, Liting Yang, Fan Yang
, Green Chem.
, 2023
, 25
, 8385
- The solution and solid state structure of {[1-(dimethylamino)-8-naphthyl]lithium·THF }2 . Jürgen Betz, Frank Hampel, Walter Bauer
, J. Chem. Soc., Dalton Trans.
, 2001
, 1876
- Basicity and bulkiness effects of 1,8-diaminonaphthalene, 8-aminoquinoline and their alkylated derivatives on the different efficiencies of η5-C5H5 and η5-C5Me5 ruthenium precatalysts in allylic etherification reactions. Giovanna Brancatelli, Dario Drommi, Giusy Feminò, Maria Saporita, Giovanni Bottari, Felice Faraone
, New J. Chem.
, 2010
, 34
, 2853
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peri-Dimethylamino substituent effects on proton transfer at carbon in α-naphthylacetate
esters: a model for mandelate racemase. Richard J. Delley, Subhajit Bandyopadhyay, Mark A. Fox, Constanze Schliehe, David R. W. Hodgson, Florian Hollfelder, Anthony J. Kirby, AnnMarie C. O'Donoghue
, Org. Biomol. Chem.
, 2012
, 10
, 590
- O- vs. N-protonation of 1-dimethylaminonaphthalene-8-ketones: formation of a peri N–C bond or a hydrogen bond to the pi-electron density of a carbonyl group. Nerea Mercadal, Stephen P. Day, Andrew Jarmyn, Mateusz B. Pitak, Simon J. Coles, Claire Wilson, Gregory J. Rees, John V. Hanna, John D. Wallis
, CrystEngComm
, 2014
, 16
, 8363
- A new family of 1,4-diaryl-1,3-butadiynes based on the “proton sponge”: synthesis, electronic and chemical properties. Ekaterina A. Filatova, Semyon V. Tsybulin, Dmitry A. Rybin, Valery A. Ozeryanskii, Anna V. Gulevskaya, Alexander F. Pozharskii, Gennady S. Borodkin
, New J. Chem.
, 2022
, 46
, 1829
- The effects of cyclic terminal groups in di- and tri-arylmethane dyes. Part 2.1 Steric and electronic effects in derivatives of Victoria Blue. Stéphane G. R. Guinot, John D. Hepworth, Mark Wainwright
, J. Chem. Soc., Perkin Trans. 2
, 1998
, 297