1878-94-0 + 993-15-7 = 940-64-7 反应条件:1.1 Reagents: Potassium Hydroxide Catalysts: Palladium Chloride Solvents: Water 标题:Palladium-Catalyzed Cross Coupling Of Organohalostannanes With Aryl Halides In Aqueous Medium 作者:Bumagin,N. A.; Roshchin,A. I. 参考文献:Russian Journal Of General Chemistry (Translation Of Zhurnal Obshchei Khimii) 日期:2000 卷标:70(1) 页码:57-63]
67028-40-4 = 940-64-7 反应条件:1.1 Reagents: Potassium Hydroxide Solvents: Ethanol; 12 H,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Rt 标题:Preparation Of Isoflavone Amide Derivatives For Treatment Of Hyperlipemia,Obesity Or Type 2 Diabetes 参考文献:China]
67028-40-4 = 940-64-7 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Ethanol,Water; 8 H,Reflux; Cooled1.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Cooled 标题:Design,Docking,Synthesis,And Characterization Of Novel N'(2-Phenoxyacetyl) Nicotinohydrazide And N'(2-Phenoxyacetyl)Isonicotinohydrazide Derivatives As Anti-Inflammatory And Analgesic Agents 作者:M,Pallavi H.; Al-Ostoot,Fares Hezam; Vivek,Hamse Kameshwar; Khanum,Shaukath Ara 参考文献:Journal Of Molecular Structure 日期:2022 卷标:1247]
专利号:WO-9002605-A1 优先权日:1988-09-02 标题:An apparatus and a method for the synthesis of peptides 发明人:MELDAL MORTEN; HOLM ARNE; BUCHARDT OLE 权利人:MELDAL MORTEN; HOLM ARNE; BUCHARDT OLE 摘要:An apparatus for use in chemical synthesis, especially peptide synthesis, comprises a synthesis chamber unit having a multiplicity of synthesis chambers, each of which has a liquid inlet and a liquid outlet, means for introducing liquid into the individual synthesis chambers and means for simultaneous removal of liquid via the liquid outlets of the synthesis chambers by regulation of the fluid pressure difference between the liquid inlets and the liquid outlets. A method for peptide synthesis using such an apparatus comprises the provision in each of the synthesis chambers of a solid-phase support material having a first, at least N-protected amino acid coupled thereto, after which a liquid deprotection reagent is introduced into the synthesis chambers. Following deprotection, the deprotection reagent is removed, after which a second, at least N-protected amino acid is introduced into each synthesis chamber in order to couple the first and second amino acids. Third, fourth, etc. amino acids may be coupled analogously. Complete removal of the deprotection reagent from the synthesis chambers and the support material can be ensured by incorporating a stable, intensely coloured dye, e.g., azorubin, in the deprotection reagent. The apparatus and the method make possible the parallel synthesis of a large number of peptides, e.g. peptides having overlapping amino acid sequences and constituting part of a longer peptide chain. The apparatus can be adapted to manual, semi-automatic or fully automatic performance of the various steps in the synthesis procedure.
专利号:US-5986132-A 优先权日:1995-11-18 标 题 :Synthesis of carboxylic acid derivatives 发明人:REEVE MAXWELL; BOWLES STEPHEN ARTHUR 权利人:BRITISH BIOTECH PHARM 摘要:Compounds of formula (I) wherein R 1 , R 2 , R 3 , R 4 , X are as defined in the specification and are prepared by elimination of one of the groups X 1 and X 2 from a compound of formula (II) wherein X 1 and X 2 each independently represent a carboxylic acid group or salt thereof, or a protected carboxylic acid group, the non-eliminated group X 1 or X 2 corresponding to the group X in the desired compound of formula (I). ##STR1##
专利号:US-6531470-B1 优先权日:1998-01-23 标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation 发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC 权利人:UPJOHN CO 摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.
专利号:US-6562844-B2 优先权日:1998-01-23 标 题:Oxazolidinone combinatorial libraries, compositions and methods of preparation 发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC 权利人:UPJOHN CO 摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.
专利号:US-9217012-B2 优先权日:2009-04-08 标题 :Inhibitors of protein tyrosine phosphatases 发明人:ZHANG ZHONG-YIN; ZHANG SHENG 权利人:ZHANG ZHONG-YIN; ZHANG SHENG; UNIV INDIANA RES & TECH CORP 摘要:Disclosed herein are compounds that selectively inhibit members of the PTP family of enzymes. Synthesized compounds demonstrated selective inhibition of TC-PTP. Also provided are methods of using the compounds and formulations containing the compounds. Also described is a fluorescence-tagged combinatorial library synthesis and screening method. And methods of using these compounds to effect enzyme activity both in cells and in vitro as well as method of using these compounds to treat diseases in human and animals.
专利号:WO-9719050-A1 优先权日:1995-11-18 标题:Synthesis of carboxylic acid derivatives