7605-44-9Relevant academic research and scientific papers
P(NMe2)3-Mediated Umpolung Alkylation and Nonylidic Olefination of α-Keto Esters
Wang, Sunewang Rixin,Radosevich, Alexander T.
, p. 3810 - 3813 (2015)
A commercial phosphorus-based reagent (P(NMe2)3) mediates umpolung alkylation of methyl aroylformates with benzylic and allylic bromides, leading to either Barbier-type addition or ylide-free olefination products upon workup. The reaction sequence is initiated by a two-electron redox addition of the tricoordinate phosphorus reagent with an α-keto ester compound (Kukhtin-Ramirez addition). A mechanistic rationale is offered for the chemoselectivity upon which the success of this nonmetal mediated C-C bond forming strategy is based.
Synthesis and biological evaluation of some stilbene derivatives
Karki, Subhas Somalingappa,Bhutle, Santosh Ramarao,Sahoo, Subhas,Reddy, Ratnakar,Balzarini, Jan,De Clercq, Erik,Darji, Satyanarayana Y.
, p. 1349 - 1356 (2012/05/05)
Several trans and cis stilbenes with substitution n the olefinic bridge were synthesized and characterized by IR, NMR and mass spectroscopy in an effort to obtain ubstances that could be more readily formulated. All the synthesized compounds were screened against Molt4/C8, CEM and L1210 cell lines. None of these compounds were ndowed with pronounced cytostatic activity. However,Schiff derivatives emerged as cytostatic agents (IC50: 0.77-10 μg/ml) that deserve further investigation. Springer Science+Business Media, LLC 2010.
Up to 96% enantioselectivities in the hydrogenation of fluorine substituted (E)-2,3-diphenylpropenoic acids over cinchonidine-modified palladium catalyst
Szollosi, Gyoergy,Herman, Beata,Felfoeldi, Karoly,Fueloep, Ferenc,Bartok, Mihaly
supporting information; experimental part, p. 2804 - 2814 (2009/10/20)
The enantioselective hydrogenation of methoxy-and fluorine-substituted (E)-2,3-diphenylpropenoic acid derivatives was studied over cinchonidine- modified, supported palladium catalysts in the absence and presence of benzylamine as additive. The fluorine substituent in the appropriate position was even more efficient than the methoxy group in increasing the optical purity of the saturated product. High enantioselectivities, up to 96%, were obtained in the hydrogenation of some disubstituted derivatives, unprecedented in the hydrogenation of prochiral unsaturated carboxylic acids over modified heterogeneous catalyst. The best optical purities were reached in the hydrogenation of derivates bearing a para-substituent on the β phenyl and an ortho-substituent on the a phenyl ring, respectively. The influence of the substituent on the β phenyl ring was attributed to the increase in the efficiency of the modifier-substrate interaction by electronic effects or to a decrease in the adsorption strength of the substituted acid over modified surface sites. The beneficial effect of the ortho-substituent on the a phenyl ring was assumed to be due to the additional interaction of this substituent with the modifier on the surface, its steric hindrance contributing only in a small part to the observed effect. These suggestions were supported by results obtained in the hydrogenations of some methyl-substituted derivatives.
Triethylamine-induced Reactions of Methyl 2,3-Dibromo-2,3-diarylpropanoates in Methanol
Badajoz, Mercedes A.,Montani, Rosana S.,Cabaleiro, Mercedes C.
, p. 124 - 125 (2007/10/03)
The title compounds undergo elimination with methanolic triethylamine to afford the corresponding debrominated olefins, most of them through an E2 stereoconvergent process.
Methyl 2,3-dibromo-2,3-diarylpropanoates. Debromination and dehydrobromination reactions
Badajoz, Mercedes A.,Montant, Rosana S.,Cabaleiro, Mercedes C.
, p. 1717 - 1722 (2007/10/03)
Rate and product studies of the iodide- and methoxide-mediated reactions of methyl (R,R)- and (R,S)-2,3-dibromo-2,3-diarylpropanoates and some of their 2- and 3-(4-substitutedphenyl)-derivatives have been carried out. The results indicate that the reactio
Photochemical Wittig Reaction of Quasi-phosphonium Ylides
Tomioka, Hideo,Ichikawa, Naoki,Murata, Hideki
, p. 193 - 195 (2007/10/02)
α-(Methoxycarbonyl)benzylidene quasi-phosphonium ylides, which are unreactive towards most carbonyl compounds, are found to undergo the Wittig reaction upon irradiation; irradiation with acyclic carbonyl compounds, e.g. benzaldehydes and acetophenones, af
Thallium in Organic Synthesis. 57. Reaction of Chalcones and Chalcone Ketals with Thallium(III) Trinitrate
Taylor, Edward C.,Conley, Richard A.,Johnson, David K.,McKillop, Alexander,Ford, Michael E.
, p. 3433 - 3436 (2007/10/02)
Treatment of chalcones (ArCH=CHCOAr') with thallium(III) trinitrate (TTN) in acidic methanol or in trimethyl orthoformate (TMOF) gives 3,3-dimethoxy-1,2-diarylpropan-1-ones (oxythallation, Ar rearrangement) and/or methyl 2,3-diaryl-3-methoxypropanoates (in situ ketal formation, oxythallation, Ar' rearrangement).The effect of substituents on Ar and Ar' on the ratio of the above rearrangement products has been examined.
