Results 11 to 20 of about 82,167 (149)
Flow microreactor synthesis in organo-fluorine chemistry [PDF]
Beilstein Journal of Organic Chemistry, 2013 Organo-fluorine compounds are the substances of considerable interest in various industrial fields due to their unique physical and chemical properties.
Hideki Amii +2 more
exaly +4 more sources
Special Feature Organo-Fluorine Chemical Science
Applied Sciences (Switzerland), 2012 Fluorine is the 13th most abundant element and, with other fluorine containing functional groups, is a most effective element in biological substances, pharmaceuticals, agrochemicals, liquid crystals, dyes, polymers and a wide range of consumer products.
Neale Jackson
exaly +4 more sources
Organo-fluorine chemistry V [PDF]
Beilstein Journal of Organic Chemistry, 2021 David O'Hagan
exaly +3 more sources
Organo-fluorine chemistry III [PDF]
Beilstein Journal of Organic Chemistry, 2013 David O'Hagan
exaly +3 more sources
Organo-fluorine chemistry II [PDF]
Beilstein Journal of Organic Chemistry, 2010 David O'Hagan
exaly +3 more sources
Themed series in organo-fluorine chemistry [PDF]
Beilstein Journal of Organic Chemistry, 2008 David O'Hagan
exaly +3 more sources
Direct Regioselective para-Fluorination via I(I)/I(III) Catalysis. [PDF]
Angew Chem Int Ed EnglA direct, para‐selective fluorination by I(I)/I(III) catalysis is disclosed that does not require substrate pre‐functionalization. This strategy leverages the Leonard link inherent to phenylpropanoate and phenylpropanamides to promote a spirocyclization/para‐selective sequence. The C3‐side chain maps onto a range of common drug scaffolds and allows the
Roblick C +5 more
europepmc +3 more sources
Borylation of Aryl Halides Induced by Visible Light Under Open-To-Air Environment. [PDF]
ChemSusChemBorylation of aryl halides was successfully achieved by a sustainable protocol which involved a purely organic confined medium, visible light as energy source under an open‐to‐air environment. Experimental and computational investigations evidenced that the reaction occurred through the formation of a ground–state complex generated by hydrogen bonding.
Herrera-Luna JC +5 more
europepmc +2 more sources
Nickel-Catalyzed Reductive Cross-Coupling of Xanthate Esters With Aryl and Alkenyl Iodides. [PDF]
ChemistryA nickel‐catalyzed reductive cross‐coupling of xanthate esters and aryl/alkenyl iodides is reported without the need for separate activators for the xanthate esters. The reaction utilizes a relatively low catalyst loading. Diarylmethanes with a good functional group variety can thus be synthesized indirectly from the corresponding benzylic alcohols ...
Vöhringer F +4 more
europepmc +2 more sources
Efficient mechanochemical synthesis of new fluorinated Schiff bases: a solvent-free, alternative to conventional method with mercury adsorption properties [PDF]
BMC ChemistryThe development of sustainable synthetic techniques is of critical importance in modern chemistry. This paper describes a mechanochemical approach to the synthesis of novel fluorinated Schiff bases via ball milling, which provides a fast, high-yield, and
Mirza T. Baig +7 more
doaj +2 more sources