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Copper‐Catalyzed Deaminative Difluoromethylation

Angewandte Chemie - International Edition, 2020
AbstractThe difluoromethyl group (CF2H) is considered to be a lipophilic and metabolically stable bioisostere of an amino (NH2) group. Therefore, methods that can rapidly convert an NH2 group into a CF2H group would be of great value to medicinal chemistry. We report herein an efficient Cu‐catalyzed approach for the conversion of alkyl pyridinium salts,
Wei Liu, Aijie Cai, Xiaojun Zeng
exaly   +3 more sources

Difluoromethylation Reactions of Organic Compounds

Chemistry - A European Journal, 2017
AbstractThe relevance of the ‐CF2H moiety has attracted considerable attention from organic synthetic and medicinal chemistry communities, because this group can act as a more lipophilic isostere of the carbinol, thiol, hydroxamic acid, or amide groups.
Sebastian Barata Vallejo   +2 more
exaly   +4 more sources

(Difluoromethyl)trimethylsilane (TMSCHF2): A Useful Difluoromethylating Nucleophilic Source

Australian Journal of Chemistry, 2021
Significant advancements have been achieved due to the excellent versatility of the commercially available (difluoromethyl)trimethylsilane (TMSCHF2) as a competent donor of the CHF2 group under nucleophilic regime.[2] It is a commercially or easily accessible liquid documenting excellent experimental manipulability due to its relatively high boiling ...
Miele M., Pace V.
openaire   +2 more sources

Synthesis of Difluoromethyl-Substituted Quinazolines through Selective Difluoromethylation

Synthesis, 2021
AbstractA highly selective difluoromethylation of quinazolines has been achieved by using commercially available ethyl bromodifluoroacetate as difluorocarbene precursor, providing the corresponding difluoromethyl substituted quinazoline derivatives with up to 83% yield.
Yiyuan Peng   +4 more
openaire   +1 more source

Difluoromethylation of Sulfonamides.

ChemInform, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
K. I. Petko   +2 more
openaire   +1 more source

Radical Difluoromethylation of Thiols with (Difluoromethyl)triphenylphosphonium Bromide

Organic Letters, 2017
A method for facile difluoromethylation of various thiols using (difluoromethyl)triphenylphosphonium bromide under mild reaction conditions is presented. The transformation proceeds in the absence of any transition metal using a bench-stable and readily accessible phosphonium salt.
Niklas B. Heine, Armido Studer
openaire   +2 more sources

Direct Difluoromethylation of Alcohols with an Electrophilic Difluoromethylated Sulfonium Ylide

Angewandte Chemie International Edition, 2016
AbstractA general method for the formation of alkyl difluoromethylethers under mild reaction conditions and with good functional‐group tolerance was developed. The development of the method was based on the invention of a stable, electrophilic, difluoromethylating reagent, difluoromethyl‐(4‐nitrophenyl)‐bis(carbomethoxy) methylide sulfonium ylide ...
Jiansheng, Zhu, Yafei, Liu, Qilong, Shen
openaire   +2 more sources

Difluoromethylation of 5-Sulfanyltetrazoles

Russian Journal of Organic Chemistry, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
K. I. Petko, L. M. Yagupol'skii
openaire   +1 more source

Copper-Catalyzed Difluoromethylation of Aryl Iodides with (Difluoromethyl)zinc Reagent

Organic Letters, 2016
The combination of difluoroiodomethane and zinc dust or diethylzinc can readily lead to (difluoromethyl)zinc reagents. Therefore, the first copper-catalyzed difluoromethylation of aryl iodides with the zinc reagents is accomplished to afford the difluoromethylated arenes.
Hiroki, Serizawa   +3 more
openaire   +2 more sources

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