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Comprehensive Evaluation of Dietary Exposure and Health Risk of Polychlorinated Naphthalenes
Environmental Science & Technology, 2022Intake from food is considered an important route of human exposure to polychlorinated naphthalenes. To our knowledge, several studies have quantified dietary exposure but only in European countries and measuring only a few of the 75 congeners.
Yongning Wu, Minghui Zheng, Lili Yang
exaly +2 more sources
Industrial & Engineering Chemistry Research, 2019
Methyl-substituted benzenes and methyl-substituted naphthalenes are important starting chemicals for organic synthesis and polymer production and superior additives of high-density fuels.
Qingya Liu, Zhenyu Liu
exaly +2 more sources
Methyl-substituted benzenes and methyl-substituted naphthalenes are important starting chemicals for organic synthesis and polymer production and superior additives of high-density fuels.
Qingya Liu, Zhenyu Liu
exaly +2 more sources
Angewandte Chemie - International Edition, 2016
We report the synthesis of orthogonally functionalized naphthalenes from simple, commercially available indanones in four steps. The developed method proceeds through a two-step process that features a thermally induced fragmentation of a cyclopropane ...
Thomas Magauer, K Hara
exaly +2 more sources
We report the synthesis of orthogonally functionalized naphthalenes from simple, commercially available indanones in four steps. The developed method proceeds through a two-step process that features a thermally induced fragmentation of a cyclopropane ...
Thomas Magauer, K Hara
exaly +2 more sources
Journal of Organic Chemistry, 2017
In this paper, we report an intramolecular cyclization of benzylic-substituted propargyl alcohols promoted by iron(III) chloride and diorganyl diselenides to give 2-organoselenyl-naphthalenes via a sequential carbon-carbon/carbon-selenium bond formation.
Davi Fernando Back, Gilson Zeni
exaly +2 more sources
In this paper, we report an intramolecular cyclization of benzylic-substituted propargyl alcohols promoted by iron(III) chloride and diorganyl diselenides to give 2-organoselenyl-naphthalenes via a sequential carbon-carbon/carbon-selenium bond formation.
Davi Fernando Back, Gilson Zeni
exaly +2 more sources
Catalytic Asymmetric Hydrogenation of Naphthalenes
Angewandte Chemie - International Edition, 2012The catalytic asymmetric hydrogenation of heteroarenes has been intensively studied during the last decade. Nowadays, various heteroaromatics, for example, indoles, pyrroles, and quinolines, can be reduced to the corresponding chiral heterocycles with ...
Ryoichi Kuwano, Shigeki Matsunaga
exaly +2 more sources
Azulene–Naphthalene, Naphthalene–Naphthalene, and Azulene–Azulene Rearrangements
The Journal of Organic Chemistry, 2022The mechanism(s) of thermal rearrangement of azulenes have been enigmatic for several decades. Herein, we have employed density functional theory (DFT) calculations at the M06-2X/6-311+G(d,p) level together with single-point calculations at the CCSD(T) level to assess possible mechanisms of the experimentally observed azulene and naphthalene ...
M. Saeed Mirzaei+2 more
openaire +2 more sources
Organic Letters, 2022
Diversity-oriented synthesis is tremendously useful for expanding the explorable chemical space but restricted by the limited available toolbox of skeleton-diversification chemistry.
Weiping Wu+3 more
semanticscholar +1 more source
Diversity-oriented synthesis is tremendously useful for expanding the explorable chemical space but restricted by the limited available toolbox of skeleton-diversification chemistry.
Weiping Wu+3 more
semanticscholar +1 more source
Photooxygenation of Naphthalene
ChemPhotoChem, 2021AbstractThe photooxygenation of naphthalene to the corresponding endoperoxide (EPO) under various conditions is described. Substantial conversion is only observed at −10 °C and after more than two days, indicating that the [4+2] cycloaddition of singlet oxygen to this acene proceeds much more slowly than corresponding reactions of substituted ...
Werner Fudickar, Torsten Linker
openaire +3 more sources
Journal of Organic Chemistry, 2020
This review analyzes the new life of a long-known reaction, the photocyclization of diarylethenes, which became a classical tool for the synthesis of phenanthrenes and their heterocyclic analogs (Mallory reaction).
A. Lvov
semanticscholar +1 more source
This review analyzes the new life of a long-known reaction, the photocyclization of diarylethenes, which became a classical tool for the synthesis of phenanthrenes and their heterocyclic analogs (Mallory reaction).
A. Lvov
semanticscholar +1 more source