In contrast to tertiary phosphine oxides, the deoxygenation of aminophosphine oxides is effectively impossible due to the need to break the immensely strong and inert PO bond in the presence of a relatively weak and more reactive PN bond. This long-standing problem in organophosphorus synthesis is solved by use of oxalyl chloride, which chemoselectively cleaves the PO bond forming a chloroph...

The synthesis and characterization of the precursor isomers trans-4-(2-(pyridin-2-yl)vinylbenzaldehyde (I), trans-4-(2-(pyridin-4-yl)vinylbenzaldehyde (II), trans-4-(2-(pyridin-2-yl)vinylbenzoic acid (III) and (E)-4-(2-(pydridin-4-yl)vinylbenzoic acid (IV) are reported. These compounds were prepared in order to obtain trans-4-((E)-2-(pyridin-2-yl)vinyl)benzamide-TEMPO (V). Compounds I and II we...

ABSTRACT. A compound S,S-bis(2-(prop-1-yn-1-yl)phenyl) ethanebis(thioate) is synthesized through one-pot synthesis. The lithiation reaction of 3-bromo-2-methylbenzo[b]thiophene by using n-butyllithium, followed conversion to the corresponding organocopper compound, and subsequent with oxalyl chloride afford target compound. chemical structure final well confirmed NMR, HRMS X-ray analysis. Meanw...

The title compound, C(29)H(35)N(3)O(4), was obtained by the reaction of (2S,4S,5S)-tert-butyl N-(4-amino-1-benzyl-3-hydr-oxy-5-phenyl-pent-yl)carbamate and picolinic acid using oxalyl chloride as a chlorinating reagent to activate the carboxyl group. In the crystal structure there are two mol-ecules in the asymmetric unit, which are aligned edge-to-face. In one mol-ecule, the pyridyl ring forms...

The use of 4-amino-5-benzyl-4H-[1,2,4]triazole-3-thiol (1) as a precursor to synthesize some new biologically active heterocycles has been found to be effective. Condensation of 1 with appropriate aldehydes gave the new Schiff bases 2a, b, which either by cyclization with thioglycolic acid gave 3a, b, or by Mannich reaction using morpholine gave 4a, b. Reaction of 1 with different halogen compo...

Oxalate catabolism is conducted by phylogenetically diverse organisms, including Methylobacterium extorquens AM1. Here, we investigate the central metabolism of this alphaproteobacterium during growth on oxalate by using proteomics, mutant characterization, and (13)C-labeling experiments. Our results confirm that energy conservation proceeds as previously described for M. extorquens AM1 and oth...

An efficient triphenylphosphine oxide-catalyzed amidation and esterification for the rapid synthesis of a series dipeptides, amides, esters is described. This reaction applicable to challenging couplings hindered carboxylic acids with weakly nucleophilic amines or alcohols, giving products in good yields (67–90%) without racemization. system employs highly reactive intermediate Ph3PCl2 as activ...

Cinchophen (I) was synthesized from pyruvic acid, aniline and benzaldehyde by Doebner synthesis. Cinchophen acid chloride (II) was synthesised from cinchophen and oxalyl chloride by acylation reaction. The 2phenylquinoline-4-carboxylic acid amide (III) was synthesized from acid chloride and ammonia by simple reaction. The 2-phenylquinoline-4-carboxylic acid amine (IV) was synthesized from cinch...

To date, only one crystal structure has been reported in the literature for oxalyl dihydrazide [H(2)N.NH.CO.CO.NH.NH(2)]. In the present paper, we report the discovery of four new polymorphs of oxalyl dihydrazide, obtained by crystallization from solution under different conditions, including the use of different crystallization solvents. All polymorphs have the trans-trans-trans conformation o...