Results 211 to 220 of about 30,128 (251)
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Synthesis of sterically hindered allyl thiocyanates: kinetic and DFT studies of their rearrangement
Tetrahedron Letters, 2016Marat Baimuratov +2 more
exaly +2 more sources
, 2015 A convenient procedure for one-pot conversion of alcohols into the corresponding alkyl thiocyanates in the presence of cross-linked poly (N-propyl-4-vinylpyridinium) thiocyanate ion [P4-VP]Pr-SCN, promoted by cyanuric chloride/dimethylformamide, is ...
M. K. Zarchi +1 more
semanticscholar +2 more sources
Activation of aryl thiocyanates followed by aryne insertion: access to 1,2-thiobenzonitriles.
Organic Letters, 2015 Palladium-catalyzed activation of carbon-sulfur bonds allows aryne insertion into aryl thiocyanates to generate new C-SAr and C-CN bonds in one step.
Martin Pawliczek +2 more
semanticscholar +2 more sources
Selectfluor™: a novel and efficient reagent for the synthesis of β-hydroxy thiocyanates
Tetrahedron Letters, 2004 A variety of epoxides undergo rapid ring opening with ammonium thiocyanate in the presence of 10 mol % Selectfluor™ in acetonitrile at room temperature to afford the corresponding β-hydroxy thiocyanates in excellent yields with high ...
B V S Reddy
exaly +2 more sources
Organic Letters, 2019
Thiocyanate compounds are key intermediates in the synthesis of pharmaceuticals and other sulfur-containing organic compounds. Herein, we first report an electrochemical protocol to synthesize vinyl thiocyanates from decarboxylative coupling of cinnamic ...
Shun Yang +3 more
semanticscholar +1 more source
Thiocyanate compounds are key intermediates in the synthesis of pharmaceuticals and other sulfur-containing organic compounds. Herein, we first report an electrochemical protocol to synthesize vinyl thiocyanates from decarboxylative coupling of cinnamic ...
Shun Yang +3 more
semanticscholar +1 more source
, 1930 The mechanism of the desulphurizing action of alkali cyanides on thiuram and xanthogen disulphides has been determined. The reaction is shown to take place in two steps, the intermediate products formed in the first step have been identified as ...
A. Cambron
semanticscholar +2 more sources
Inorganica Chimica Acta, 2019
Novel mononuclear lanthanide thiocyanates with 2,2′;6′,2″-terpyridine (terpy), namely isomorphic complexes [Ln(terpy)2(NCS)3] (Ln = Y, Eu, Tb and Dy) were prepared and studied.
S. Petrosyants +7 more
semanticscholar +1 more source
Novel mononuclear lanthanide thiocyanates with 2,2′;6′,2″-terpyridine (terpy), namely isomorphic complexes [Ln(terpy)2(NCS)3] (Ln = Y, Eu, Tb and Dy) were prepared and studied.
S. Petrosyants +7 more
semanticscholar +1 more source
Recent advances in the chemistry of organic thiocyanates.
Chemical Society Reviews, 2016Thomas Castanheiro +3 more
semanticscholar +1 more source