While the equation above is correct, it is not very useful for incremental updates since the equation above updates the checksum C, rather than the 1’s complement of the checksum, ̃C, which is the value stored in the checksum field. In addition, it suffers because the notation does not clearly specify that all arithmetic, including the unary negation, must be performed one’s complement, and so i...

A series of 1-phenyl-3-aryl-5-(4-(3-propanoloxy) phenyl)-1H-pyrazoles were synthesized from chalcones and studied for their in vitro antibacterial activity. Chalcones i.e.,1-aryl-3-(4hydroxyphenyl) prop-2-en-1-ones (1) on reaction with phenyl hydrazine in presence of acetic acid and few drops of HCl yielded the corresponding 1-phenyl-3-aryl-5-(4-hydroxyphenyl)-1H-pyrazoles (2) which on further ...

A series of 1-phenyl-3-aryl-5-(4-(2-ethanoloxy) phenyl)-1H-pyrazoles were synthesized from chalcones and studied for their in vitro antibacterial activity. Chalcones i.e.,1-aryl-3-(4hydroxyphenyl) prop-2-en-1-ones, 1 on reaction with phenyl hydrazine yielded the corresponding 1-phenyl-3-aryl-5-(4-hydroxyphenyl)-1H-pyrazoles 2 which on further reaction with 3-chloroethanol furnished the title co...

A catalyst, based on a biarylphosphine ligand, for the Pd-catalyzed cross-coupling reactions of amides and aryl mesylates is described. This system allows an array of aryl and heteroaryl mesylates to be transformed into the corresponding N-aryl amides in moderate to excellent yields.

1,3-dibromo-5,5-dimethylhydantoin (dbh), as a cheap and commercially available reagent, is efficiently able to catalyze the synthesis of polyhydroquinoline derivatives and 12-aryl-8,9,10,12-tetrahydro[a] xanthene-11-ones via one-pot multi-component reactions. this novel synthetic method has the advantages of low cost and availability of the catalyst, short reaction times, high to excellent yiel...

The aryl(imino)stannylene MesTer[N(IDipp)]Sn could be obtained by treating NHILi (NHI=N(IDipp), IDipp=C[N-(2,6-iPr2C6H3)CH]2) with MesTerSnCl (MesTer=2,6-Mes2C6H3) and offers a unique reactivity pattern compared to conventional single site tetrylene catalyzed CO2 reduction reactions. Sn(II) center, stabilized the NHI ligand enabled sequestration valorization of C1 feedstock stoichiometrically, ...

Other than triarylamines, which are protonated by strong acids both at their N-atom and aromatic rings, pyrrole its N-substituted derivatives were exclusively the carbon atoms of heteroaromatic rings. Whereas with trifluoromethane sulfonic acid (TFS) stable pyrrolium salts obtained, weaker trifluoroacetic (TFA) oligomers formed. E.g., from N-(tert-butyl)pyrrole a dimeric compound could be unamb...

Solid phase synthesis of 1,3,4-oxadiazin-5(6R)-one and 1,3,4-oxadiazol-2-one scaffolds from resin-bound acyl hydrazides is described. We demonstrate here that the reactions of resin-bound aryl or hetero-aromatic acyl hydrazides with 2-substituted-2-bromoacetic acids and 4-nitrophenyl chloroformate and subsequent treatment with DIEA lead to intramolecular cyclization reactions to produce six-mem...