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Sequential and regioselective Friedel–Crafts reactions of
gem-dihalogenocyclopropanecarbonyl chlorides with benzenes for
the synthesis of 4-aryl-1-naphthol derivatives
. Yoshinori Nishii, Yoo Tanabe
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 477
- CXX.—The aluminium-mercury couple. Part III. Chlorination of aromatic hydrocarbons in presence of the couple. The constitution of the dichlorotoluenes. Julius B. Cohen, Henry D. Dakin
, J. Chem. Soc., Trans.
, 1901
, 79
, 1111
- Solvatochromic shifts of single-walled carbon nanotubes in nonpolar microenvironments. Carlos A. Silvera-Batista, Randy K. Wang, Philip Weinberg, Kirk J. Ziegler
, Phys. Chem. Chem. Phys.
, 2010
, 12
, 6990
- Continuous photochemical benzylic bromination using in situ generated Br2: process intensification towards optimal PMI and throughput. Alexander Steiner, Jason D. Williams, Oscar de Frutos, Juan A. Rincón, Carlos Mateos, C. Oliver Kappe
, Green Chem.
, 2020
, 22
, 448
- Dielectric relaxation and dipole-dipole interaction. J. Sobhanadri
, Trans. Faraday Soc.
, 1960
, 56
, 965
- Cyclic phosphopeptides for interference with Grb2 SH2 domain signal transduction prepared by ring-closing metathesis and phosphorylation. Frank J. Dekker, Nico J. de Mol, Marcel J. E. Fischer, Johan Kemmink, Rob M. J. Liskamp
, Org. Biomol. Chem.
, 2003
, 1
, 3297
- Perfectly imperfect: a review of chemical tools for exciton engineering in single-walled carbon nanotubes. Dawid Janas
, Mater. Horiz.
, 2020
, 7
, 2860
- SERS-based detection of an organochlorine pesticide through surface plasmon-induced C–C coupling. Douglas S. Lopes, Ester V. Miranda, Rômulo A. Ando, Paola Corio
, Environ. Sci.: Nano
, 2023
, 10
, 1920
- XCVI.—The cumulative effect of the chlorine atom and the methyl and sulphonyl chloride groups on substitution in the benzene nucleus. Part I. William Davies
, J. Chem. Soc., Trans.
, 1921
, 119
, 853
- CXXXIV.—The chlorination of the dichlorotoluenes in presence of the aluminium-mercury couple. The constitution of the trichlorotoluenes. Julius B. Cohen, Henry D. Dakin
, J. Chem. Soc., Trans.
, 1902
, 81
, 1324