27992-27-4Relevant articles and documents
Synthesis of 3,5-disubstituted pyrazole derivatives with a carbamate function
Velikorodov,Kovalev,Krivosheev
, p. 1208 - 1209 (2009)
One-pot reaction of 1,3-dipolar cycloaddition of aryldiazamethanes generated in situ from the sodium salts of tosylhydrazones of benzaldehyde, p-nitro-, p-methoxy-, and 3,4-dimethoxybenzaldehyde to propargyl-N-phenyl carbamate under heating led to the for
Synthesis of new pyrazolines and their biological evaluation as antimicrobial agents
Hamadi, Naoufel Ben,Haouas, Amel,Methamem, Mahbouba,Msaddek, Moncef
, p. 563 - 565,3 (2020/09/16)
2-Diazopropane and diazo compounds derived from aromatic aldehydes were reacted with aromatic esters of 3- hydroxyprop-1-yne to give the aromatic esters of 5-hydroxymethyl-3-substituted pyrazoles. Anti-microbial screening using the Gram positive (Staphylo
Laser flash photolysis study of phenylcarbene, o-tolylcarbene and mesitylcarbene
Admasu, Atnaf,Platz, Matthew S.,Marcinek, Andrzej,Michalak, Jacek,Gudmundsdottir, Anna Dora,Gebicki, Jerzy
, p. 207 - 220 (2007/10/03)
Laser flash photolysis (LFP, XeCl, 308 nm, 20 ns) of phenyldiazomethane (PDM), o-tolydiazomethane (TDM) and mesitydiazomethane (MDM) produces phenylcarbene (PC), o-tolycarbene (TC) and mesitylcarbene (MSC), respectively. Transient spectra of PC and TC cou
