Results 1 to 10 of about 2,380,041 (121)

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, Aiichiro Nagaki, Jun-ichi Yoshida   +2 more
doaj   +4 more sources

Themed series in organo-fluorine chemistry [PDF]

Beilstein Journal of Organic Chemistry, 2008
Peer ...
David O'Hagan
doaj   +6 more sources

Organo-fluorine chemistry II [PDF]

Beilstein Journal of Organic Chemistry, 2010
Peer ...
David O'Hagan
doaj   +5 more sources

Organo-fluorine chemistry V [PDF]

Beilstein Journal of Organic Chemistry, 2021
David O’Hagan
doaj   +3 more sources

Organo-fluorine chemistry III [PDF]

Beilstein Journal of Organic Chemistry, 2013
David O'Hagan
doaj   +3 more sources

Direct Regioselective para-Fluorination via I(I)/I(III) Catalysis. [PDF]

Angew Chem Int Ed Engl
A 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, Bendix JD, Hilton TA, Bussmann K, Daniliuc CG, Gilmour R.   +5 more
europepmc   +3 more sources

Borylation of Aryl Halides Induced by Visible Light Under Open-To-Air Environment. [PDF]

ChemSusChem
Borylation 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, López-Paz JL, Díaz Díaz D, Jiménez MC, Sampedro D, Pérez-Ruiz R.   +5 more
europepmc   +2 more sources

Nickel-Catalyzed Reductive Cross-Coupling of Xanthate Esters With Aryl and Alkenyl Iodides. [PDF]

Chemistry
A 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, Zwettler K, Sharapa DI, Studt F, Fleischer I.   +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 Chemistry
The 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, Mariam T. Sayed, Reem Aledamat, Sumyah Hassan, Alaa AlReyashi, Naheed Sidiq, Siham Y. Al-Qaradawi, Mohamed F. Mady   +7 more
doaj   +2 more sources

Joy and Flustration with Organofluorine Compounds – A Fluorous Autobiography

CHIMIA, 2014
An overview is given about our work on fluoro-organic compounds, published or described in PhD theses between 1977 and 2013. After a discussion of structural F-effects and F-tagging applications the material is ordered by the various areas of ...
Dieter Seebach
doaj   +1 more source