2,3,4,5,6-五氟甲苯置于溴体系中,化学反应 18.0H,反应生成α-溴-2,3,4,5,6-五氟甲基苯酸酯 参考文献:可见光促进的wohl-Ziegler在无溶剂条件下用n-溴代琥珀酰亚胺对有机分子进行官能化 标题:可见光促进的wohl-Ziegler在无溶剂条件下用n-溴代琥珀酰亚胺对有机分子进行官能化 摘要:Abstractmagnified Imagethe Visible‐light‐induced Transformation Of Toluenes With N‐bromosuccinimide (Nbs) Under Solvent‐free Reaction Conditions (Sfrc) Was Studied. The Reaction Took Place In Spite Of The Very Restricted Molecular Motion; Toluenes Could Be Regioselectively Converted To Benzyl Bromides. Selective Radical‐chain Reactions With Nbs Were Carried Out In Liquid/liquid And In Solid/solid Systems; Furthermore,Reactions Could Be Performed In The Presence Of Air. The Radical Scavenger Tempo (=2,2,6,6‐tetramethylpiperidin‐1‐yloxy) Completely Suppressed The Side‐chain Bromination Of Toluenes With Nbs Under Sfrc. Electron‐withdrawing Groups Decreased The Reactivity Of The Toluenes,And The Hammett Reaction Constant ρ+=−1.7 Indicated Involvement Of Polar Radical Intermediates With Electrophilic Character. Doi:10.1002/hlca.200800308
专利号:US-11034664-B1 优先权日:2020-05-11 标题 :Synthesis of cyclic carbonate monomers 发明人:PARK NATHANIEL H; HEDRICK JAMES L; PIUNOVA VICTORIA A; ARRECHEA PEDRO; ERDMANN TIM 权利人:IBM 摘要:Techniques regarding the synthesis of cyclic carbonate monomers are provided. For example, one or more embodiments described herein can comprise a method, which can include cyclizing a functionalized diol monomer with N,N′-carbonyldiimidazole, wherein the cyclizing produces a cyclic carbonate monomer and an imidazole carbamate. The method can also include activating the imidazole carbamate with an acid, wherein the activating promotes cyclization of the imidazole carbamate into the cyclic carbonate monomer.
专利号:EP-0274314-B1 优先权日:1986-12-11 标题 :Process for the preparation of pentafluorophenylmethyl 2,2-dimethyl-3-formylcyclopropanecarboxylate, and its use in the synthesis of pesticidal products 摘要:As new chemical products, the products (I): in all the possible stereoisomeric forms and mixtures of these stereo- isomers and their application to the synthesis of pesticide products.
专利号:US-2025163020-A1 优先权日:2022-08-31 标 题:Chiral Synthesis of Nornicotine and Nicotine 发明人:STRAKOVÃ? KAROLÃ?NA; MÜLLER DOMINIK SIMON; VAN VEGTEN CORNELIS HENDRIK; ZELLER FLORIAN DANIEL; DEBNAR THOMAS 权利人:SIEGFRIED AG; CONTRAF NICOTEX TOBACCO GMBH 摘要:The present invention relates to a method of producing nornicotine through enantioselective hydrosilylation of myosmine and a composition produced thereby, as well as a composition comprising nornicotine and a catalyst, wherein the catalyst is an organic chiral Lewis base, and a catalyst. The present invention also relates to a method of producing nicotine or a salt thereof from myosmine through enantioselective hydrosilylation of myosmine to nornicotine and further reacting the nornicotine to nicotine or a salt thereof, and a composition produced thereby, as well as a composition comprising nicotine, or a salt thereof, and a catalyst, wherein the catalyst.
专利号:US-8193392-B2 优先权日:2005-07-29 标 题:Method for enantioselective synthesis of phosphorus-stereogenic phosphines 发明人:SCRIBAN CORINA; GLUECK DAVID S 权利人:SCRIBAN CORINA; GLUECK DAVID S; DARTMOUTH COLLEGE 摘要:The present invention relates to a process for preparing an enantioenriched phosphorus-stereogenic, tertiary phosphine. Secondary phosphines are contacted with an alkyl halide and base in the presence of a chiral metal catalyst thereby producing the enantioenriched phosphorus-stereogenic, tertiary phosphine for subsequent use in homogeneous catalysis reactions.
专利号:WO-2021083438-A1 优先权日:2019-10-30 标 题:Inhibitors of purine nucleoside phosphorylase - synthesis and use thereof for treatment of t-cell acute lymphoblastic leukemia and lymphoma 发明人:SKACEL JAN; JANEBA ZLATKO; MERTLIKOVA KAISEROVA HELENA 权利人:USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR V V I 摘要:The present invention relates to new compounds of general formula I, their synthesis, their pharmaceutically acceptable salts, and their use in treatment of T-cell acute lymphoblastic leukemia and lymphoma.
专利号:US-6576454-B2 优先权日:1998-01-23 标 题:Modified enzymes and their use for peptide synthesis 发明人:JONES J BRYAN 权利人:UNIV TORONTO 摘要:The present invention relates to modified enzymes with one or more amino acid residues from an enzyme being replaced by cysteine residues, where at least some of the cysteine residues are modified by replacing thiol hydrogen in the cysteine residue with a thiol side chain to form a modified enzyme, wherein the modified enzyme has high esterase and low amidase activity. Also, a method of producing the modified enzymes is provided. The present invention also relates to a method for using the modified enzymes in peptide synthesis.
摘要:Ayad, T.; Pirat, J.-L.; Virieux, D., Science of Synthesis Knowledge Updates, (2022) 1, 343. 参考文献:10.1007/bf01192883 摘要:Veningerová M, Uhnák J, Prachar V, Kovacicová J. Chlorinated phenols in human milk. Z Lebensm Unters Forsch. 1996 Sep;203(3):309–10. doi: 10.1007/bf01192883. 参考文献:10.1007/bf01369601 摘要:Imamura T, Kage S, Kudo K, Jitsufuchi N, Nagata T. A case of drowning linked to ingested sulfides — a report with animal experiments. International Journal of Legal Medicine. 1996 Mar;109(1):42–4. doi: 10.1007/bf01369601. 参考文献:10.1007/s00420-004-0523-4 摘要:Ben-Brik E, Jérôme L, Arnaud I, Yous S, Labat L, Haguenoer JM, Multigner L. Exposure to glycol ethers in a population of French men evaluated by measurement of urinary alkoxycarboxylic acids. International Archives of Occupational and Environmental Health. 2004 May 26;77(5):368–72. doi: 10.1007/s00420-004-0523-4. 参考文献:10.2165/00044011-199816040-00006 摘要:Deray G, Bagnis C, Brouard R, Necciari J, Leenhardt AF, Raymond F, Baumelou A. Clopidogrel activities in patients with renal function impairment. Clin Drug Investig. 1998;16(4):319–28. doi: 10.2165/00044011-199816040-00006.