33906-65-9 = 960-71-4 反应条件:1.1 -78 °C -> 200 °C; 15 Min,200 °C 标题:Iron Complexes Of A Proton-Responsive Scs Pincer Ligand With A Sensitive Electronic Structure 作者:Skubi,Kazimer L.; Hooper,Reagan X.; Mercado,Brandon Q.; Bollmeyer,Melissa M.; Macmillan,Samantha N.; Et Al 参考文献:Inorganic Chemistry 日期:2022 卷标:61(3) 页码:1644-1658]
87005-57-0 = 960-71-4 [标题:Reaction Conditions 标题:Preparation Of Triarylboranes 参考文献:United States]
= 960-71-4 反应条件:1.1 Reagents: Boron Trifluoride Etherate,Magnesium,Iodine Solvents: Xylene 标题:Cost-Effective Preparation Method Of Triphenylboron Using Magnesium Powder And Bromobenzene 参考文献:China]
= 960-71-4 反应条件:1.1 Reagents: Boron Trifluoride 标题:Hydroxylamine-O-Sulfonic Acid 作者:Erdik,Ender; Saczewski,Jaroslaw 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2013 卷标:1 页码:1-10]
33906-65-9 = 960-71-4 反应条件:1.1 Reagents: Mesitylene; 3 H,170 °C 标题:Preparation Of Triarylboranes And Their Complexes By Thermal Decomposition Of Trialkylammonium Borates 参考文献:Japan]
971-66-4 = 960-71-4 反应条件:1.1 Reagents: Mesitylene; 180 °C 标题:Preparation Of Ionic-Impurity-Free Triarylborane Complexes 参考文献:Japan]
= 960-71-4 反应条件:1.1 Reagents: Boron Trifluoride Etherate,Magnesium,Iodine Solvents: Diethyl Ether 标题:Organoboranes. 44. A Convenient,Highly Efficient Synthesis Of Triorganylboranes Via A Modified Organometallic Route 作者:Brown,Herbert C.; Racherla,Uday S. 参考文献:Journal Of Organic Chemistry 日期:1986 卷标:51(4) 页码:427-32]
= 960-71-4 [标题:Reaction Conditions 标题:Boron Compounds. V. Hydrogenation Of Trialkyl- And Triarylboranes 作者:Koester,Roland; Bruno,Guenter; Binger,Paul 参考文献:Justus Liebigs Annalen Der Chemie 日期:1961 卷标:644 页码:1-22]
= 960-71-4 反应条件:1.1 Reagents: Triisopropyl Borate,Sodium Solvents: Benzene,Cyclohexane; Rt -> 80 °C; 40 Min,80 °C 标题:Preparation Method Of Triarylborane 参考文献:China]
3262-89-3 = 960-71-4 反应条件:1.1 Reagents: Potassium Carbonate Solvents: Dimethylformamide; 1 H,130 °C 标题:Unexpected Formation Of Triphenylborane From Phenylboronic Acid And Its Use As An Intermediate In Palladium-Catalyzed Cross Coupling Reaction 作者:Motokura,Ken; Fukuda,Takuma; Manaka,Yuichi 参考文献:Chemistryselect 日期:2019 卷标:4(35) 页码:10501-10505]
= 960-71-4 反应条件:1.1 Reagents: Boron Trifluoride Solvents: Diethyl Ether; 0 °C; 2 H,0 °C; 0 °C -> Rt; Overnight,Rt 标题:Controlling The Lewis Acidity And Polymerizing Effectively Prevent Frustrated Lewis Pairs From Deactivation In The Hydrogenation Of Terminal Alkynes 作者:Liu,Qiang; Yang,Liu; Yao,Chenfei; Geng,Jiao; Wu,Youting; Et Al 参考文献:Organic Letters 日期:2021 卷标:23(9) 页码:3685-3690]
= 960-71-4 反应条件:1.1 Reagents: Boron Trifluoride Etherate,Magnesium Solvents: Diethyl Ether 标题:Ultrasonics In Organoborane Chemistry. Rapid Synthesis Of Triorganylboranes Via A Modified Organometallic Route 作者:Brown,Herbert C.; Racherla,Uday S. 参考文献:Tetrahedron Letters 日期:1985 卷标:26(36) 页码:4311-14]
501-65-5 + 4151-77-3 = 960-71-4 反应条件:1.1 Catalysts: Acetic Acid 标题:Bora-Aromatic Systems. Vi. Dehalogenation Of Organoboron Dihalides In The Search For Borenes 作者:Eisch,John J.; Becker,Hans P. 参考文献:Journal Of Organometallic Chemistry 日期:1979 卷标:171(2) 页码:141-53
专利号:US-11753503-B2 优先权日:2018-05-17 标 题:Supported onium salts as initiators for the synthesis of polycarbonates by copolymerization of CO2 with epoxides 发明人:FENG XIAOSHUANG; PATIL NAGANATHA; LUCIANI CAROLINE; GNANOU YVES; HADJICHRISTIDIS NIKOS 权利人:UNIV KING ABDULLAH SCI & TECH 摘要:Supported onium salts used as initiators for the synthesis of polycarbonates by copolymerization of carbon dioxide with epoxides are described. Embodiments of the present disclosure describe initiators comprising an insoluble portion including an onium cation attached to an insoluble support; and an anion, wherein the anion is a counter-ion to the onium cation. Embodiments further describe methods of making polycarbonates using the initiator, methods of making initiators, and the like.
专利号:US-2004006137-A1 优先权日:2002-06-28 标题:Asymmetric synthesis of amino-pyrrolidinones and a crystalline, free-base amino-pyrrolidinone 发明人:WALTERMIRE ROBERT E; CAMPAGNA SILVIO; SAVAGE SCOTT A; BORDAWEKAR SHAILENDRA; MADUSKUIE THOMAS P; DESIKAN SRIDHAR; ANDERSON STEPHEN R 摘要:A novel process for the asymmetric synthesis of an amino-pyrrolidinone of the type shown below is described. n n n These compounds are useful as intermediates for MMP and TACE inhibitors. n Crystalline, free-base form of Compound J ((2R)-2-((3R)-3-amino-3-{-[(2-methyl-4-quinolinyl)methoxy]phenyl}-2-oxopyrrolidinyl)-N-hydroxy-4-methylpentanamide): n n n which is useful as a TACE inhibitor, pharmaceutical compositions comprising the same, and methods of using the same for treating inflammatory diseases are also described.
专利号:US-11713329-B2 优先权日:2018-12-10 标 题 :Intermediates useful in the preparation of halichondrin compounds and methods for preparing the same 发明人:XU WEIPING 权利人:BEIJING TIENYI LUFU PHARMATECH CO LTD 摘要:The invention relates to intermediates useful in the preparation of halichondrin compounds, methods for preparing the same and use thereof, such as halichondrins, eribulin, or their analogs. The intermediates, the methods and use thereof are used for the synthesis of the C20-C26 fragment of halichondrin compounds. The raw materials in the synthetic route of the invention are cheap and easily obtained, the sources and the qualities of the raw materials are reliable. The choice of the methods useful in the synthesis of chiral central structures are based on the structural characteristics of the reactants, thus effectively improving the synthesis efficiency, reducing the difficulties and risks of product quality control, and avoiding the use of highly toxic and expensive organotin catalysts to significantly decrease costs and improve environmental friendliness.
专利号:US-7271231-B2 优先权日:1995-01-24 标 题 :Polymerization of olefins 发明人:BROOKHART MAURICE S; JOHNSON LYNDA KAYE; KILLIAN CHRISTOPHER MOORE 权利人:DU PONT 摘要:Disclosed herein are processes for polymerizing ethylene, acyclic olefins, and/or selected cyclic olefins, and optionally selected olefinic esters or carboxylic acids, and other monomers. The polymerizations are catalyzed by selected transition metal compounds, and sometimes other co-catalysts. Since some of the polymerizations exhibit some characteristics of living polymerizations, block copolymers can be readily made. Many of the polymers produced are often novel, particularly in regard to their microstructure, which gives some of them unusual properties. Numerous novel catalysts are disclosed, as well as some novel processes for making them. The polymers made are useful as elastomers, molding resins, in adhesives, etc. Also described herein is the synthesis of linear α-olefins by the oligomerization of ethylene using as a catalyst system a combination a nickel compound having a selected α-diimine ligand and a selected Lewis or Bronsted acid, or by contacting selected α-diimine nickel complexes with ethylene.
专利号:US-8697902-B2 优先权日:2008-06-17 标 题:Preparation of nitriles from ethylenically unsaturated compounds 发明人:MASTROIANNI SERGIO 权利人:MASTROIANNI SERGIO; RHODIA OPERATIONS 摘要:A process for the hydrocyanation of a hydrocarbon-based compound having at least one site of ethylenic unsaturation into a nitrile compound includes reaction thereof, in a liquid medium, with hydrogen cyanide in the presence of a catalyst containing a metal element selected from among the transition metals and an organophosphorus ligand, wherein the organophosphorus ligand is a compound of formula (I): n n n n n n n n n n The subject process is particularly useful for the synthesis of adiponitrile from butadiene.
专利号:US-8716507-B2 优先权日:2008-10-31 标题 :Iron(II) catalysts containing diimino-diphosphine tetradentate ligands and their synthesis 发明人:MIKHAILINE ALEXANDRE; FREUTEL FRIEDERIKE; SUI-SENG CHRISTINE; MEYER NILS; MORRIS ROBERT H; LAGADITIS PARASKEVI OLYMPIA 权利人:MIKHAILINE ALEXANDRE; FREUTEL FRIEDERIKE; SUI-SENG CHRISTINE; MEYER NILS; MORRIS ROBERT H; LAGADITIS PARASKEVI OLYMPIA; GOVERNING COUNCIL OF UNIVERSITY OF TORONTO 摘要:New hexa-coordinate iron (II) complexes comprising compounds of formula (I) are described. These compounds comprise a tetradentate ligand with donor atoms comprising nitrogen and phosphorus. These complexes are shown for the first time to be useful catalysts for the hydrogenation of ketones, aldehydes, or imines to produce alcohols or amines, and the asymmetric hydrogenation of prochiral ketones or imines to produce non-racemic alcohols or amines. The source of the hydrogen can be hydrogen gas or a hydrogen-donating molecule such as isopropanol or hydrogen-donating mixture such as formic acid and an amine depending on the structure of the catalyst. In certain embodiments, the axial ligands on the catalyst comprise organonitrile ligands, carbonyl ligands, isonitrile ligands, or combinations thereof. The catalysts and the preparation thereof are disclosed. A reaction using phosphine and diamine precursors that is templated by the iron ion is the preferred route to the catalysts.
摘要:Stolley, R. M.; Louie, J., Science of Synthesis Knowledge Updates, (2013) 2, 39. 摘要:Ramirez y Medina, I.-M.; Kipke, W.; Makow, J.; Staubitz, A., Science of Synthesis Knowledge Updates, (2020) 2, 33. 摘要:Ulfkjær, A.; Pittelkow, M., Science of Synthesis Knowledge Updates, (2018) 1, 134. 摘要:Tauchert, M. E., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 1, 313. 摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198