نتایج جستجو برای: oxazolidinone chiral

تعداد نتایج: 37927  

Journal: :Organic letters 1999
M T Crimmins K A Emmitte

[formula: see text] The enantioselective total synthesis of (+)-laurencin 1 is achieved in 18 steps from (S)-(+)-4-benzyl-3-benzyloxyacetyl-2-oxazolidinone. The key steps in this synthesis are an asymmetric glycolate alkylation leading to acyl oxazolidinone 2 and a subsequent ring-closing olefin metathesis to construct the oxocene core of 1. The approach to medium ring ethers utilized in this s...

Journal: :Organic & biomolecular chemistry 2015
Aurélie Paulen Véronique Gasser Françoise Hoegy Quentin Perraud Bénédicte Pesset Isabelle J Schalk Gaëtan L A Mislin

Pseudomonas aeruginosa is a Gram-negative pathogenic bacterium responsible for severe infections in which resistance to most of the approved families of antibiotics is increasing. Oxazolidinone antibiotics are active against many Gram-positive bacteria, but are only weakly active against Gram-negative pathogens. We describe the synthesis of conjugates between a catechol moiety and oxazolidinone...

Journal: :the iranian journal of pharmaceutical research 0
farrin sattary javid pharmaceutical chemistry department, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. alireza shafaati pharmaceutical chemistry department, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. afshin zarghi pharmaceutical chemistry department, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

one of the problems encountered in ce separations of basic compounds is the adsorption of analytes onto the negatively charged capillary wall which could lead to poor repeatability of migration time and peak area. additionally, separation of enantiomers of chiral of basic drugs is commonly carried out in low ph buffer which contributes to strong ionic interaction of the cationic drug ions with ...

Journal: :Antimicrobial agents and chemotherapy 2018
Erica Yookyung Lee Aisling R Caffrey

Several studies have suggested the risk of thrombocytopenia with tedizolid, a second-in-class oxazolidinone antibiotic (approved June 2014), is less than that observed with linezolid (first-in-class oxazolidinone). Using data from the Food and Drug Administration adverse event reporting system (July 2014 through December 2016), we observed significantly increased risks of thrombocytopenia of si...

Journal: :Angewandte Chemie 2004
Frank Glorius Nick Spielkamp Sigrid Holle Richard Goddard Christian W Lehmann

available and the reaction has the potential for the simultaneous creation of multiple stereocenters. Here we describe an efficient and unprecedented auxiliary-based method for the asymmetric hydrogenation of substituted pyridines (YR= N), which enables the stereoselective formation of piperidines with up to four new chiral centers in a single operation (Scheme 2a). The heterogeneous catalytic ...

Journal: :Antimicrobial agents and chemotherapy 2009
Stephan Schmidt Sreedharan Nair Sabarinath April Barbour Darren Abbanat Prasarn Manitpisitkul Sue Sha Hartmut Derendorf

Linezolid is the first FDA-approved oxazolidinone with activity against clinically important gram-positive pathogens, including methicillin (meticillin)-resistant Staphylococcus aureus (MRSA). RWJ-416457 is a new oxazolidinone with an antimicrobial spectrum similar to that of linezolid. The goal of the present study was to develop a general pharmacokinetic (PK)-pharmacodynamic (PD) model that a...

Journal: :RNA 1999
N B Matassova M V Rodnina R Endermann H P Kroll U Pleiss H Wild W Wintermeyer

Oxazolidinones are antibacterial agents that act primarily against gram-positive bacteria by inhibiting protein synthesis. The binding of oxazolidinones to 70S ribosomes from Escherichia coli was studied by both UV-induced cross-linking using an azido derivative of oxazolidinone and chemical footprinting using dimethyl sulphate. Oxazolidinone binding sites were found on both 30S and 50S subunit...

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 ...

Journal: :Chemical communications 2012
Srinivas Banala Roland G Huber Thomas Müller Martin Fechtel Klaus R Liedl Bernhard Kräutler

A hexafullereno-diporphyrinoid was obtained in a sequence of cycloaddition steps using porphyrins programmed for [4+2]-cycloaddition reactions and C(60)-fullerene.

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