نتایج جستجو برای: chiral compounds

تعداد نتایج: 262114  

Journal: :Chirality 2005
Amanda L Jenkins William A Hedgepeth

Recent American Food and Drug Administration guidelines have effectively determined that mixtures of chiral compounds can no longer be brought to the pharmaceuticals marketplace. These guidelines require a means for chiral detection and compound separation. This article describes separation and detection of chiral pharmaceuticals using HPLC with circular dichroism detection. Two over-the-counte...

Journal: :Chemical Science 2023

Chiral separation has already become a crucial topic for effectively utilizing superfluous racemates synthesized by chemical means and satisfying the growing requirements producing enantiopure chiral compounds. However, remarkably...

Journal: :Journal of agricultural and food chemistry 2010
Xiaofen Du Chad Finn Michael C Qian

The distribution of volatile constituents in ancestral genotypes of 'Marion' blackberry's pedigree was investigated over two growing seasons. Each genotype in the pedigree had a specific volatile composition. Red raspberry was dominated by norisoprenoids, lactones, and acids. 'Logan' and 'Olallie' also had a norisoprenoid dominance but at much lower concentrations. The concentration of norisopr...

Journal: :Chemistry 2014
Shiqing Xu Akimichi Oda Ei-ichi Negishi

Chiral compounds arising from the replacement of hydrogen atoms by deuterium are very important in organic chemistry and biochemistry. Some of these chiral compounds have a non-measurable specific rotation, owing to very small differences between the isotopomeric groups, and exhibit cryptochirality. This particular class of compounds is difficult to synthesize and characterize. Herein, we prese...

Journal: :Journal of chromatography. A 2002
Jared L Anderson Jie Ding Ryan D McCulla William S Jenks Daniel W Armstrong

The separation of 17 chiral sulfoxides and eight chiral sulfinate esters by gas chromatography (GC) on four derivatized cyclodextrin chiral stationary phases (CSPs) (Chiraldex G-TA, G-BP, G-PN, B-DM) is presented. Many of these compounds are structural isomers or part of a homologous series. Differences in enantioselectivity of the methyl phenyl sulfoxide isomers on the derivatized gamma cyclod...

Journal: :Physical review letters 2011
T Aaltonen B Álvarez González S Amerio D Amidei A Anastassov A Annovi J Antos G Apollinari J A Appel A Apresyan T Arisawa A Artikov J Asaadi W Ashmanskas B Auerbach A Aurisano F Azfar W Badgett A Barbaro-Galtieri V E Barnes B A Barnett P Barria P Bartos M Bauce G Bauer F Bedeschi D Beecher S Behari G Bellettini J Bellinger D Benjamin A Beretvas A Bhatti M Binkley D Bisello I Bizjak K R Bland B Blumenfeld A Bocci A Bodek D Bortoletto J Boudreau A Boveia B Brau L Brigliadori A Brisuda C Bromberg E Brucken M Bucciantonio J Budagov H S Budd S Budd K Burkett G Busetto P Bussey A Buzatu C Calancha S Camarda M Campanelli M Campbell F Canelli A Canepa B Carls D Carlsmith R Carosi S Carrillo S Carron B Casal M Casarsa A Castro P Catastini D Cauz V Cavaliere M Cavalli-Sforza A Cerri L Cerrito Y C Chen M Chertok G Chiarelli G Chlachidze F Chlebana K Cho D Chokheli J P Chou W H Chung Y S Chung C I Ciobanu M A Ciocci A Clark G Compostella M E Convery J Conway M Corbo M Cordelli C A Cox D J Cox F Crescioli C Cuenca Almenar J Cuevas R Culbertson D Dagenhart N d'Ascenzo M Datta P de Barbaro S De Cecco G De Lorenzo M Dell'Orso C Deluca L Demortier J Deng M Deninno F Devoto M d'Errico A Di Canto B Di Ruzza J R Dittmann M D'Onofrio S Donati P Dong M Dorigo T Dorigo K Ebina A Elagin A Eppig R Erbacher D Errede S Errede N Ershaidat R Eusebi H C Fang S Farrington M Feindt J P Fernandez C Ferrazza R Field G Flanagan R Forrest M J Frank M Franklin J C Freeman Y Funakoshi I Furic M Gallinaro J Galyardt J E Garcia A F Garfinkel P Garosi H Gerberich E Gerchtein S Giagu V Giakoumopoulou P Giannetti K Gibson C M Ginsburg N Giokaris P Giromini M Giunta G Giurgiu V Glagolev D Glenzinski M Gold D Goldin N Goldschmidt A Golossanov G Gomez G Gomez-Ceballos M Goncharov O González I Gorelov A T Goshaw K Goulianos A Gresele S Grinstein C Grosso-Pilcher R C Group J Guimaraes da Costa Z Gunay-Unalan C Haber S R Hahn E Halkiadakis A Hamaguchi J Y Han F Happacher K Hara D Hare M Hare R F Harr K Hatakeyama C Hays M Heck J Heinrich M Herndon S Hewamanage D Hidas A Hocker W Hopkins D Horn S Hou R E Hughes M Hurwitz U Husemann N Hussain M Hussein J Huston G Introzzi M Iori A Ivanov E James D Jang B Jayatilaka E J Jeon M K Jha S Jindariani W Johnson M Jones K K Joo S Y Jun T R Junk T Kamon P E Karchin Y Kato W Ketchum J Keung V Khotilovich B Kilminster D H Kim H S Kim H W Kim J E Kim M J Kim S B Kim S H Kim Y K Kim N Kimura M Kirby S Klimenko K Kondo D J Kong J Konigsberg A V Kotwal M Kreps J Kroll D Krop N Krumnack M Kruse V Krutelyov T Kuhr M Kurata S Kwang A T Laasanen S Lami S Lammel M Lancaster R L Lander K Lannon A Lath G Latino I Lazzizzera T LeCompte E Lee H S Lee J S Lee S W Lee S Leo S Leone J D Lewis C-J Lin J Linacre M Lindgren E Lipeles A Lister D O Litvintsev C Liu Q Liu T Liu S Lockwitz N S Lockyer A Loginov D Lucchesi J Lueck P Lujan P Lukens G Lungu J Lys R Lysak R Madrak K Maeshima K Makhoul P Maksimovic S Malik G Manca A Manousakis-Katsikakis F Margaroli C Marino M Martínez R Martínez-Ballarín P Mastrandrea M Mathis M E Mattson P Mazzanti K S McFarland P McIntyre R McNulty A Mehta P Mehtala A Menzione C Mesropian T Miao D Mietlicki A Mitra H Miyake S Moed N Moggi M N Mondragon C S Moon R Moore M J Morello J Morlock P Movilla Fernandez A Mukherjee Th Muller P Murat M Mussini J Nachtman Y Nagai J Naganoma I Nakano A Napier J Nett C Neu M S Neubauer J Nielsen L Nodulman O Norniella E Nurse L Oakes S H Oh Y D Oh I Oksuzian T Okusawa R Orava L Ortolan S Pagan Griso C Pagliarone E Palencia V Papadimitriou A A Paramonov J Patrick G Pauletta M Paulini C Paus D E Pellett A Penzo T J Phillips G Piacentino E Pianori J Pilot K Pitts C Plager L Pondrom K Potamianos O Poukhov F Prokoshin A Pronko F Ptohos E Pueschel G Punzi J Pursley A Rahaman V Ramakrishnan N Ranjan I Redondo P Renton M Rescigno F Rimondi L Ristori A Robson T Rodrigo T Rodriguez E Rogers S Rolli R Roser M Rossi F Rubbo F Ruffini A Ruiz J Russ V Rusu A Safonov W K Sakumoto Y Sakurai L Santi L Sartori K Sato V Saveliev A Savoy-Navarro P Schlabach A Schmidt E E Schmidt M P Schmidt M Schmitt T Schwarz L Scodellaro A Scribano F Scuri A Sedov S Seidel Y Seiya A Semenov F Sforza A Sfyrla S Z Shalhout T Shears P F Shepard M Shimojima S Shiraishi M Shochet I Shreyber A Simonenko P Sinervo A Sissakian K Sliwa J R Smith F D Snider A Soha S Somalwar V Sorin P Squillacioti M Stancari M Stanitzki R St Denis B Stelzer O Stelzer-Chilton D Stentz J Strologas G L Strycker Y Sudo A Sukhanov I Suslov K Takemasa Y Takeuchi J Tang M Tecchio P K Teng J Thom J Thome G A Thompson E Thomson P Ttito-Guzmán S Tkaczyk D Toback S Tokar K Tollefson T Tomura D Tonelli S Torre D Torretta P Totaro M Trovato Y Tu F Ukegawa S Uozumi A Varganov F Vázquez G Velev C Vellidis M Vidal I Vila R Vilar J Vizán M Vogel G Volpi P Wagner R L Wagner T Wakisaka R Wallny S M Wang A Warburton D Waters M Weinberger W C Wester B Whitehouse D Whiteson A B Wicklund E Wicklund S Wilbur F Wick H H Williams J S Wilson P Wilson B L Winer P Wittich S Wolbers H Wolfe T Wright X Wu Z Wu K Yamamoto J Yamaoka T Yang

We report the most sensitive direct search for pair production of fourth-generation bottomlike chiral quarks (b') each decaying promptly to tW. We search for an excess of events with an electron or muon, at least five jets (one identified as due to a b or c quark), and an imbalance of transverse momentum by using data from pp collisions collected by the CDF II detector at Fermilab with an integ...

2006
R. J. Baxter

It has been known for some time that the Boltzmann weights of the chiral Potts model can be parametrized in terms of hyperelliptic functions, but as yet no such parametrization has been applied to the partition and correlation functions. Here we show that for N = 3 the function S(t p) that occurs in the recent calculation of the order parameters can be expressed quite simply in terms of such a ...

2002
Karin Wiberg Björn Sigurdsson

Many persistent organic pollutants (POPs) are chiral. These pollutants are generally released into the environment as racemates, but frequently undergo alterations in enantiomeric composition as soon as they are subjected to life chemistry processes. Enantiospecific analysis of chiral POPs is important since enantiomers of chiral compounds often exhibit differences in biological activity, and m...

Journal: :Organic & biomolecular chemistry 2011
Jérôme Vachon Steven Harthong Erwann Jeanneau Christophe Aronica Nicolas Vanthuyne Christian Roussel Jean-Pierre Dutasta

Inherently chiral phosphonatocavitands with various bridging moieties at their wide rim were synthesized. Optical resolution by chiral HPLC was performed with cavitand 8 to afford enantiopure compounds (+)-8 and (-)-8. The molecular structures of hosts 8 and 12 were determined by X-ray diffraction. The host properties were investigated by (1)H and (31)P NMR spectroscopy. The phosphonatocavitand...

2018
Aitor Urosa Ignacio E Tobal Ángela P de la Granja M Carmen Capitán R F Moro Isidro S Marcos Narciso M Garrido Francisca Sanz Emilio Calle David Díez

A novel approach to the production of chiral 1,3-cyclohexadienals has been developed. The organocatalysed asymmetric reaction of different β-disubstituted-α,β-unsaturated aldehydes with a chiral α,β-unsaturated aldehyde in the presence of a Jørgensen-Hayashi organocatalyst provides easy and stereocontrolled access to the cyclohexadienal backbone. This method allows for the synthesis of potentia...

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