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Articles 31 - 43 of 43
Full-Text Articles in Organic Chemistry
A Simplified Direct Lipid Mixing Lipoplex Preparation: Comparison Of Liposomal-, Dimethylsulfoxide-, And Ethanol-Based Methods, Joseph Meisel, George Gokel
A Simplified Direct Lipid Mixing Lipoplex Preparation: Comparison Of Liposomal-, Dimethylsulfoxide-, And Ethanol-Based Methods, Joseph Meisel, George Gokel
Chemistry & Biochemistry Faculty Works
Established transfection methodology often uses commercial reagents, which must be formed into liposomes in a sequence of about half a dozen steps. The simplified method reported here is a direct lipid mixing approach that requires fewer steps, less manipulation, and is less time-consuming. Results are comparable to those obtained with more commonly used methods, as judged by a variety of analytical techniques and by comparisons of transfection results. The method reported here may be applied to non-liposome-forming compounds, thereby greatly expanding the range of structures that can be tested for transfection ability.
Uplc–Qtof–Ms And Nmr Analyses Of Graviola (Annona Muricata) Leaves, Ingrid De Moraes, Paulo Ribeiro, Flávio Schmidt, Kirley Canuto, Guilherme Zocolo, Edy De Brito, Rensheng Luo, Kristy Richards, Kevin Tran, Robert Smith
Uplc–Qtof–Ms And Nmr Analyses Of Graviola (Annona Muricata) Leaves, Ingrid De Moraes, Paulo Ribeiro, Flávio Schmidt, Kirley Canuto, Guilherme Zocolo, Edy De Brito, Rensheng Luo, Kristy Richards, Kevin Tran, Robert Smith
Chemistry & Biochemistry Faculty Works
No abstract provided.
Stereocontrolled 1,2-Cis Glycosylation As The Driving Force Of Progress In Synthetic Carbohydrate Chemistry, Swati Nigudkar, Alexei Demchenko
Stereocontrolled 1,2-Cis Glycosylation As The Driving Force Of Progress In Synthetic Carbohydrate Chemistry, Swati Nigudkar, Alexei Demchenko
Chemistry & Biochemistry Faculty Works
Recent developments in stereoselective 1,2-cis glycosylation that have emerged during the past decade are surveyed herein. For detailed coverage of the previous achievements in the field the reader is referred to our earlier reviews: A. V. Demchenko, Curr. Org. Chem., 2003, 7, 35–79 and Synlett, 2003, 1225–1240.
Relay Cross Metathesis Reactions Of Vinylphosphonates, Raj Malla, Jeremy Ridenour, Christopher Spilling
Relay Cross Metathesis Reactions Of Vinylphosphonates, Raj Malla, Jeremy Ridenour, Christopher Spilling
Chemistry & Biochemistry Faculty Works
Dimethyl (β-substituted) vinylphosphonates do not readily undergo cross metathesis reactions with Grubbs catalyst and terminal alkenes. However, the corresponding mono- or diallyl vinylphosphonate esters undergo facile cross metathesis reactions. The improved reactivity is attributed to a relay step in the cross metathesis reaction mechanism.
New Bis(Imino)Pyridine Complexes Of Iron(Ii) And Iron(Iii), And Their Catalytic Activity In The Mukaiyama Aldol Reaction, Pushkar Shejwalkar, Nigam Rath, Eike Bauer
New Bis(Imino)Pyridine Complexes Of Iron(Ii) And Iron(Iii), And Their Catalytic Activity In The Mukaiyama Aldol Reaction, Pushkar Shejwalkar, Nigam Rath, Eike Bauer
Chemistry & Biochemistry Faculty Works
New iron(II) and iron(III) complexes bearing bis(imino)pyridine ligands were synthesized and successfully applied to the Mukaiyama aldol reaction. The two complexes [FeCl2 L] (L = bis(imino)pyridine ligand, 55% isolated yield) and [LFe(μCl)3FeCl3] (76%) were obtained employing FeCl2 and FeCl3 iron sources, respectively, and characterized by elemental analyses, mass spectrometry, IR spectroscopy and, one example, by X-ray diffraction. The two new iron complexes were subsequently employed as catalysts in the Mukaiyama aldol reaction after abstraction of two chlorides by AgSbF6 to obtain the aldol products in 43% to virtually quantitative yield (CH2Cl2 solvent, room temperature, 3.5 to 16 h reaction time). …
2-Allylphenyl Glycosides As Complementary Building Blocks For Oligosaccharide And Glycoconjugate Synthesis, Hemali Premathilake, Alexei Demchenko
2-Allylphenyl Glycosides As Complementary Building Blocks For Oligosaccharide And Glycoconjugate Synthesis, Hemali Premathilake, Alexei Demchenko
Chemistry & Biochemistry Faculty Works
The O-allylphenyl (AP) anomeric moiety was investigated as a new leaving group that can be activated for chemical glycosylation under a variety of conditions, through both direct and remote pathways. Differentiation between the two activation pathways was achieved in a mechanistic study. The orthogonal-type activation of the AP moiety along with common thioglycosides allows for the execution of efficient oligosaccharide assembly.
Effect Of A Strategically Positioned Methoxy Substituent On The Photochemistry Of 3-Aryl-3h-1-Oxacyclopenta[L]Phenanthren-2-Ones, Roshini Thumpakara, Binoy Jose, Perupparampil Unnikrishnan, Sreedharan Prathapan, Nigam Rath
Effect Of A Strategically Positioned Methoxy Substituent On The Photochemistry Of 3-Aryl-3h-1-Oxacyclopenta[L]Phenanthren-2-Ones, Roshini Thumpakara, Binoy Jose, Perupparampil Unnikrishnan, Sreedharan Prathapan, Nigam Rath
Chemistry & Biochemistry Faculty Works
Irradiation of 3-methoxy-3-aryl-3H-1-oxacyclopenta[l]phenanthren-2-one derivatives 5a–d resulted in singlet-mediated decarbonylation reaction leading to the formation of phenanthrene derivatives 9a–d. The structure of the photoproduct was unequivocally established on the basis of X-ray crystallographic analysis.
(1e,3e)-1,4-Bis(4-Methoxyphenyl)Buta1,3-Diene, Gopinathan Narayan, Nigam Rath, Suresh Das
(1e,3e)-1,4-Bis(4-Methoxyphenyl)Buta1,3-Diene, Gopinathan Narayan, Nigam Rath, Suresh Das
Chemistry & Biochemistry Faculty Works
The title compound, C18H18O2, which exhibits blue emission in the solid state, is an intermediate in the preparation of liquid crystals and polymers. The molecule is located on an inversion centre. In the crystal, molecules are arranged in a herringbone motif.
2,4,6-TriphenylAniline, Onome Ugono, Stephanie Cowin, Alicia Beatty
2,4,6-TriphenylAniline, Onome Ugono, Stephanie Cowin, Alicia Beatty
Chemistry & Biochemistry Faculty Works
Individual molecules of the title compound, C24H19N, do not participate in hydrogen-bonding interactions due to the steric bulk of the phenyl rings ortho to the amine. The dihedral angles between the central ring and the pendant rings are 68.26 (10), 55.28 (10) and 30.61 (11)°.
New Chiral Phosphoramidite Complexes Of Iron As Catalytic Precursors In The Oxidation Of Activated Methylene Groups, Pushkar Shejwalkar, Nigam Rath, Eike Bauer
New Chiral Phosphoramidite Complexes Of Iron As Catalytic Precursors In The Oxidation Of Activated Methylene Groups, Pushkar Shejwalkar, Nigam Rath, Eike Bauer
Chemistry & Biochemistry Faculty Works
New phosphoramidite complexes of iron were synthesized and structurally characterized. Reaction of the known chiral phosphoramidites (RO)2PNR’2 (R = binaphthyl, R’ = CH3, 1a; R = binaphthyl, R’ = benzyl, 1b) with [FeBr(Cp)(CO)2] afforded the title compounds [FeBr(Cp)(CO)(1a,b)] (4a,b) in 34 and 65 % isolated yields as mixtures of diastereomers, since both the metal and the ligand are stereogenic. Similarly, reaction of 1b with [Fe(Cp)I(CO)2] in the presence of catalytic [Fe(Cp)(CO)2]2 afforded [Fe(Cp)I(CO)(1b)] (5b) in 81% yield as a mixture of diastereomers. The molecular structures of 4a, 4b and 5 were determined, revealing a pseudo octahedral coordination geometry about the …
Critically Evaluated Thermochemical Properties Of Polycyclic Aromatic Hydrocarbons, María Roux, Manuel Temprado, James Chickos, Yatsuhisa Nagano
Critically Evaluated Thermochemical Properties Of Polycyclic Aromatic Hydrocarbons, María Roux, Manuel Temprado, James Chickos, Yatsuhisa Nagano
Chemistry & Biochemistry Faculty Works
No abstract provided.
Modeling The Physical Properties Of A Homologous Series On The Melting Temperatures And Densities Of N-Alkanes And Their Simple Alkyl-Derivatives, Antun Rubčić, Jasna Rubčić, James Chickos
Modeling The Physical Properties Of A Homologous Series On The Melting Temperatures And Densities Of N-Alkanes And Their Simple Alkyl-Derivatives, Antun Rubčić, Jasna Rubčić, James Chickos
Chemistry & Biochemistry Faculty Works
No abstract provided.
2-Phenyl-3-(5,6,7,7a-Tetrahydro-1h,3h-Pyrrolo[1,2-C]Oxazol-3-Ylidene)-1-Propene-1,1-Dicarbonitrile And 4-(4-Methoxyphenyl)-2,6-Bis(Methylthio)Pyridine-3-Carbonitrile, M. George, S. Das, C.V. Ashokan, N.P. Rath, M.V. George
2-Phenyl-3-(5,6,7,7a-Tetrahydro-1h,3h-Pyrrolo[1,2-C]Oxazol-3-Ylidene)-1-Propene-1,1-Dicarbonitrile And 4-(4-Methoxyphenyl)-2,6-Bis(Methylthio)Pyridine-3-Carbonitrile, M. George, S. Das, C.V. Ashokan, N.P. Rath, M.V. George
Chemistry & Biochemistry Faculty Works
The reaction of 3-aryl-2-cyano-5,5-bis(methylthio)penta-2,4-dienenitrile, (1), with (L)-(-)-2-hydroxymethylpyrrolidine, (2), gave two types of product, the normal substitution product, (3), and a pyridine derivative, (4). The structures of two representative examples, 2-phenyl-3-(5,6,7,7a-tetrahydro1H,3H-pyrrolo[1,2-c]oxazol-3-ylidene)-1-propene-1,1-dicarbonitrile, (3a), as its hemibenzene solvate, C17H14N3O.0.5C6H6, and 4-(4-methoxyphenyl)-2,6-bis(methylthio)pyridine-3-carbonitrile, (4b), C15H14N2OS2, have been unambiguously established by X-ray crystallographic analysis. The molecular packing of (4b) involves loosly held dimers with S1...S1' distances of 3.424 (1) Å.