CAS: 1517-63-1; Phenyl(P-Tolyl)Methanol

相似化合物

134-84-9 885-77-8 91-01-0

上下游产品

CAS号3262-89-3 苯硼酸酐 | CAS号104-87-0 对甲基苯甲醛 | CAS号98-80-6 苯硼酸 | CAS号934-56-5 三甲基苯基锡 | CAS号5720-05-8 对甲基苯基硼酸 | CAS号100-52-7 苯甲醛 | CAS号134-84-9 4-甲基二苯甲酮 | CAS号4463-41-6 4-甲基苯硼酸-1,3-丙二醇酯 | CAS号6843-66-9 二苯基二甲氧基硅烷 | CAS号2996-92-1 苯基三甲氧基硅烷 | CAS号55095-21-1 [(4-甲基苯基)(苯基)甲基]胺盐酸盐 | CAS号220322-74-7 1-methyl-4-(1-p... | CAS号19804-27-4 托拉代尔 | CAS号620-83-7 4-甲基二苯甲烷 | CAS号134-84-9 4-甲基二苯甲酮 | CAS号37858-00-7 4,4'-(oxybis(ph... | CAS号16271-22-0 3,3',5,5'-Tetra... | CAS号110047-35-3 bis(4-methoxy-3... | CAS号1083-30-3 1,3-二苯基丙-1-酮 | CAS号14097-24-6 1,3-二苯基丙-1-醇

4-甲基二苯甲酮置于lithium Tert-Butoxide体系中,用 异丙醇 用作溶剂,化学反应 24.0H,以91%的收率获得4-甲基二苯甲醇
参考文献:在温和条件下用异丙醇光驱动 Mpv 型将芳基酮/醛还原为醇
标题:在温和条件下用异丙醇光驱动 Mpv 型将芳基酮/醛还原为醇
摘要:醇是药物,农用化学品和精细化学品的多功能结构基序.在绿色化学方面,非常需要开发更可持续和更具成本效益的将酮/醛转化为醇的工艺.在此,开发了一种使用异丙醇作为还原剂和溶剂,在t-Buoli存在下,在室温空气气氛下将酮/醛还原为醇的直接光驱动策略.这种操作简单的光促进 Meerwein-Ponndorf-Verley (Mpv) 型还原可用于生产各种苯甲醇衍生物,也可应用于生物活性分子和 Peek 模型化合物,展示了其应用潜力.
Doi:10.1039/d1Gc02449C

专利信息

专利号:US-8859765-B2
优先权日:2011-11-30
标 题:Process for the manufacture of chiral catalysts and their salts
发明人：WU PING-YU; HENSCHKE JULIAN PAUL
权利人:SCINOPHARM TAIWAN LTD
摘要:The present invention provides efficient and economical methods for synthesis of (−)-2-exo-morpholinoisoborne-10-thiol, its enantiomer, and related chiral catalysts. Novel compounds and methods of asymmetric synthesis are also disclosed.

专利号:US-7176297-B2
优先权日:2002-04-08
标 题:Photoactivatable silane compounds and methods for their synthesis and use
发明人：LI HANDONG; MCGALL GLENN H
权利人:AFFYMETRIX INC
摘要:In one aspect of the invention, photoactivatable silane compounds and methods for their synthesis and use are provided. In one embodiment, the photoactivatable silane compounds synthesized are represented by a formula: PG-LS-SN, wherein PG is a photoactivatable group, LS is a linkage and spacer group, and SN is a silane group. The silanes allow the photoactivatable silane compounds to be covalently bound to the surface of a substrate such as silica. The photoactivatable group forms a hydrophobic layer that can be photochemically cross-linked with a layer of hydrophilic functional polymers. In another embodiment, a method is disclosed to synthesize a substrate of hydrophobic layers and hydrophilic functional polymer layers thereafter onto glass surfaces. An array of biopolymers such as nucleic acids and peptides may then be covalently attached to the substrate using photolithography and biopolymer synthesis.

专利号:US-5780692-A
优先权日:1995-12-28
标 题:Process for producing optically active benzhydrol compounds
发明人：SAKAGUCHI MINZO; IMAI TAKASHI; MIURA TAKASHI; YAMAZAKI TETSURO
权利人:TAKASAGO PERFUMERY CO LTD
摘要:A process for producing a benzhydrol compound (II) which comprises hydrogenating a benzophenone compound (I) in the presence of a hydrogenation catalyst consisting of a transition metal complex, a base and an optically active diamine compound: (I) (II) wherein R1 to R10 each represents H, OH, C1-4 alkyl, C1-4 alkoxy, C1-4 alkanoyl, etc., R2 and R3, and R8 and R9 may form -CH=CH-CH=CH-, or any two of R1 to R9 adjacent to each other may be bonded to thereby form -OCH2O- or -(CH2)3-. By using this process, optically active benzhydrol compounds which have a high purity and are useful as, for example, intermediates in the synthesis of drugs can be produced by simple procedures.

专利号:US-11279734-B2
优先权日:2017-12-01
标 题:Solution-phase affinity selection of inhibitors from combinatorial peptide libraries
发明人：PENTELUTE BRADLEY L; TOUTI FAYCAL
权利人:MASSACHUSETTS INST TECHNOLOGY
摘要:The present invention provides novel peptides (e.g., peptides, macrocyclic peptides, mini-proteins) that modulate protein-protein interactions or salts thereof, and methods of making and using the inventive peptides. In some embodiments, the peptides are high affinity inhibitors (e.g., K D of at most 100 nM, at most 10 nM, at most 1 nM) of a protein-protein interaction. In certain embodiments, these peptides interfere with p53-MDM2 binding interactions (e.g., by binding to MDM2 (GenBank® Gene ID: 4193)). In some embodiments, the peptides interfere with the dimerization of the C-terminal domain of the human immunodeficiency virus (HIV) capsid protein (C-CA), comprising residues 146-231 of the HIV capsid protein (e.g., by binding to the C-terminal domain of the HIV capsid protein (C-CA), thereby inhibiting the dimeric interface of HIV capsid protein, thereby inhibiting viral assembly). These inventive peptides were rapidly generated and identified using novel methods described herein comprising combinatorial peptide synthesis and/or solution affinity selection.

专利号:CN-109053754-B
优先权日:2018-08-15
标 题:Synthesis of polysubstituted chroman compounds based on dearomatization cycloaddition strategy of biomass-derived 2,5-dimethylfuran

专利号:CN-103073372-A
优先权日:2011-10-25
标 题 :Method for Catalytic Synthesis of Amine Compounds by Functionalized Ionic Liquid