Organic Process Research & Development
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
Inhaltsverzeichnis
- 659
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Octavio Augusto Ceva Antunes| 2009
- 660
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Some Items of Interest to Process R&D Chemists and EngineersMcLaughlin, Mark / Rubio, Silvina García / Pfeiffer, Matthew et al. | 2009
- 669
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A Review of U.S. Patents in the Field of Organic Process Development Published During February and March 2009Turner, Keith et al. | 2009
- 683
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Preparative Chromatography Technique in the Removal of Isostructural Genotoxic Impurity in Rizatriptan: Use of Physicochemical Descriptors of Solute and AdsorbentMaddula, Srinivasula Reddy / Kharkar, Manoj / Manudhane, Kushal et al. | 2009
- 690
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Model-Based Solvent Selection during Conceptual Process Design of a New Drug Manufacturing ProcessHsieh, Daniel / Marchut, Alexander J. / Wei, Chenkou et al. | 2009
- 698
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Facile, Fast and Safe Process Development of Nitration and Bromination Reactions Using Continuous Flow ReactorsPelleter, Jacques / Renaud, Fabrice et al. | 2009
- 706
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Development of an Acid-Washable Tag for the Separation of Enantiomers from BioresolutionsBrossat, Maude / Moody, Thomas S. / de Nanteuil, Florian et al. | 2009
- 710
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A Facile, One-Pot Synthesis of Lacidipine Using in Situ Generation of Wittig IntermediatesPrasada Raju, V. V. N. K. V. / Ravindra, Vedantham / Mathad, Vijayavitthal T. et al. | 2009
- 716
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The Process Development of Ravuconazole: An Efficient Multikilogram Scale Preparation of an Antifungal Agent(1)Pesti, Jaan et al. | 2009
- 716
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The Process Development of Ravuconazole: An Efficient Multikilogram Scale Preparation of an Antifungal AgentPesti, Jaan / Chen, Chien-Kuang / Spangler, Lori et al. | 2009
- 729
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Process Development for A Novel Pleuromutilin-Derived AntibioticAndemichael, Yemane / Chen, Jun / Clawson, Jacalyn S. et al. | 2009
- 739
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Scale-Up of Trisodium [(3β,5β,12α)-3-[[4(S)-4-[Bis[2-[bis[(carboxy-kO)methyl]amino-kN]ethyl]amino-kN]-4-(carboxy-kO)-1-oxobutyl]amino]-12-hydroxycholan-24-oato(6-)]gadolinate(3-)], a Gd(III) Complex under Development As a Contrast Agent for MRI Coronary AngiographyAnelli, Pier Lucio / Brocchetta, Marino / Lattuada, Luciano et al. | 2009
- 739
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Scale-Up of Trisodium [(3 beta ,5 beta ,12 alpha )-3-[[4(S)-4-[Bis[2-[bis[(carboxy-kO)methyl]amino-kN]ethyl]-amino-kN]-4-(carboxy-kO)-1-oxobutyl]amino]-12-hydroxycholan-24-oato(6-)]gadolinate(3-)], a Gd(III) Complex under Development As a Contrast Agent for MRI Coronary AngiographyAnelli, P.L. / Brocchetta, M. / Lattuada, L. et al. | 2009
- 747
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Adaptation of an Exothermic and Acylazide-Involving Synthesis Sequence to Microreactor TechnologyRumi, Luigi / Pfleger, Christophe / Spurr, Paul et al. | 2009
- 751
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A Convergent Synthesis of AR-C123196 Utilising Reaction Between a Cyclic Carbonate and a Phenol for Aryl Alkyl Ether FormationAllsop, Glyn L. / Cole, Andrea J. / Giles, Melvyn E. et al. | 2009
- 760
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Practical Synthetic Method of (2Z,3E)-1,4-Diphenylbutadiene T-2639, an Inhibitor of Plasminogen Activator Inhibitor-1 (PAI-1) ProductionMiyazaki, Hiroshi / Ohmizu, Hiroshi / Ogiku, Tsuyoshi et al. | 2009
- 764
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Development of an Open-Air and Robust Method for Large-Scale Palladium-Catalyzed Cyanation of Aryl Halides: The Use of i-PrOH to Prevent Catalyst Poisoning by OxygenRen, Yunlai / Liu, Zhifei / He, Shebin et al. | 2009
- 769
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A Simple, Efficient, Green, Cost Effective and Chemoselective Process for the Esterification of Carboxylic AcidsRekha, Vamsi V. / Ramani, Modukuri V. / Ratnamala, A. et al. | 2009
- 769
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A Simple, Efficient, Green, Cost Effective and Chemoselective Process for the Esterification of Carboxlic AcidsRekha, V.V. / Ramani, M.V. / Ratnamala, A. et al. | 2009
- 774
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Development of a Supply Route for the Synthesis of an iNOS Inhibitor: Complications of the Key SN2 ReactionRassias, Geracimos / Hermitage, Stephen A. / Sanganee, Mahesh J. et al. | 2009
- 781
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Kilogram-Scale Synthesis of the CXCR4 Antagonist GSK812397Boggs, Sharon / Elitzin, Vassil I. / Gudmundsson, Kristjan et al. | 2009
- 786
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Controlling the Genotoxins Ethyl Chloride and Methyl Chloride Formed During the Preparation of Amine Hydrochloride Salts from Solutions of Ethanol and MethanolYang, Qiang / Haney, Brian P. / Vaux, Alexander et al. | 2009
- 792
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An Improved and Single Pot Process for the Production of Quetiapine Hemifumarate Substantially Free from Potential ImpuritiesNiphade, Navnath C. / Mali, Anil C. / Pandit, Bhushan S. et al. | 2009
- 798
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Orthogonal Experiments in the Development of Organic Synthetic ProcessesCarlson, Rolf / Simonsen, Geir / Descomps, Alexandre et al. | 2009
- 804
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An Improved Synthesis of Antiulcerative Drug: TenatoprazoleSripathi, Somaiah / Bojja, Ramachandra Reddy / Karnati, Venugopal Reddy et al. | 2009
- 807
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Practical Synthesis of 5-Fluoro-2-(piperidin-4-yloxy)pyrimidin-4-amine, a Key Intermediate in the Preparation of Potent Deoxycytidine Kinase InhibitorsZhang, Haiming / Yan, Jie / Kanamarlapudi, Ramanaiah C. et al. | 2009
- 812
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An Efficient Process of Racemization of 3-(Carbamoylmethyl)-5-methylhexanoic acid: A Pregabalin IntermediateChavan, Anil B. / Maikap, Golak C. / Gurjar, Mukund K. et al. | 2009
- 812
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An Efficient Process of Racemization of 3-(Carbamolmethyl)-5-methylhexanoic acid: A Pregabalin IntermediateChavan, A.B. / Maikap, G.C. / Gurjar, M.K. et al. | 2009
- 815
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An Improved Process for the Preparation of Diphenylmethyl 7 beta -Phenylacetamido-3-hydroxymethyl-3-cephem-4-carboxylateYu, K. / Sun, N. / Fang, S. et al. | 2009
- 815
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An Improved Process for the Preparation of Diphenylmethyl 7β-Phenylacetamido-3-hydroxymethyl-3-cephem-4-carboxylateYu, Keping / Sun, Nan / Fang, Shanzong et al. | 2009
- 820
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First Multigram Preparation of SCP-123, A Novel Water-Soluble AnalgesicMiao, Lei / Xu, Liang / Narducy, Kenneth W. et al. | 2009