Results 71 to 80 of about 300 (133)

Barton-Kellogg Olefination of (CF₃S)₂C=S and Subsequent Cyclopropanation for the Installation of Bulky Bis(trifluoromethylthio)methylene Group. [PDF]

JACS Au
Sun J, Sun Y, Gu YC, Lin JH, Xiao JC.
europepmc   +1 more source

Strain-release trifluoromethoxylation and pentafluorosulfanoxylation of [1.1.0]bicyclobutanes: expanded access to fluorinated cyclobutane hybrid bioisosteres. [PDF]

Chem Commun (Camb)
Kraemer Y, Stephens AM, Buldt JA, Young A, McLoughlin CP, Fettinger JC, Holder LM, Pitts CR.   +7 more
europepmc   +1 more source

Dual-regioselective direct C(sp²)-arylation of unprotected β-enamino esters with 2-indolylmethanols catalyzed by Brønsted acid. [PDF]

RSC Adv
Song QC, Zhao PH, Xing YX, Bao CX, Chen LY, Li Y.   +5 more
europepmc   +1 more source

Copper-Catalyzed, N-Directed Csp³-H Trifluoromethylthiolation (-SCF₃) and Trifluoromethylselenation (-SeCF₃). [PDF]

J Am Chem Soc, 2019
Modak A, Pinter EN, Cook SP.
europepmc   +1 more source

Chiral Copper Catalysis in Enantioselective Domino Reactions. [PDF]

Molecules
Pellissier H.
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Asymmetric Synthesis and Applications of Chiral Organoselenium Compounds: A Review. [PDF]

Molecules
Jian Y, Singh T, Andersson PG, Zhou T.
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C3 Selective chalcogenation and fluorination of pyridine using classic Zincke imine intermediates. [PDF]

Nat Commun
Li S, Tang J, Shi Y, Yan M, Fu Y, Su Z, Xu J, Xue W, Zheng X, Ge Y, Li R, Chen H, Fu H.   +12 more
europepmc   +1 more source

Advances in radical peroxidation with hydroperoxides. [PDF]

Beilstein J Org Chem
Bityukov OV, Serdyuchenko PY, Kirillov AS, Nikishin GI, Vil' VA, Terent'ev AO.   +5 more
europepmc   +1 more source

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Electrophilic Trifluoromethylthiolation of Carbonyl Compounds

Chemistry - A European Journal, 2014
AbstractA general method for the α‐trifluoromethylthiolation of carbonyl compounds, without prefunctionalization, has been developed. Aldehydes, ketones, esters, amides, keto‐esters, alkaloids, and steroids have been trifluoromethylthiolated with good yields.
Luc Zimmer, Thierry Billard
exaly   +4 more sources

Recent advances in trifluoromethylthiolation using nucleophilic trifluoromethylthiolating reagents

Tetrahedron Letters, 2016
Abstract With regard to the high lipophilicity of the trifluoromethylthio group (CF 3 S–), there is a growing interest in the development of efficient methods for the incorporation of CF 3 S moiety onto organic molecules. In this review, recent advances in trifluoromethylthiolation using nucleophilic trifluoromethylthiolating reagents are discussed ...
Zhiqiang Weng, Huidong Zheng, Yangjie Huang   +2 more
exaly   +2 more sources