专利号:US-5302595-A 优先权日:1988-10-04 标题:Muscarinic receptor antagonists 发明人:CROSS PETER E; MACKENZIE ALEXANDER R 权利人:PFIZER 摘要:Compounds of the formula I ##STR1## wherein X, Y and v are as defined below, novel intermediates used in their synthesis, and the pharmaceutically acceptable salts of such compounds and intermediates. The compounds of formula I and the novel intermediates used in their synthesis are muscarinic receptor antagonists that are selected for smooth muscle muscarinic sites and are useful in the prevention and treatment of diseases associated with altered motility or tone of smooth muscle, such as irritable bowel syndrome, diverticular disease, urinary incontinence, aesophageal achalasia, and chronic obstructive airways disease.
专利号:US-9518067-B2 优先权日:2013-03-27 标题 :Trifluoroborate mass spectrometric tags 发明人:HUANG YUMEI 权利人:CELLMOSAIC INC 摘要:The invention provides compositions and methods for mass spectrometric (MS), organic synthesis, and applications of organo-trifluoroborate, for example, as mass tags for use in negative ion mode. When subject to MS fragmentation, organo-trifluoroborates preferentially undergo neutral losses of hydrogen fluoride (HF) or boron trifluoride (BF 3 ) molecules, transferring the negative charge to the rest of the molecule. Such a fragmentation pattern is used to detect and quantitate analytes of interest after derivatization with organo-trifluoroborates.
专利号:CN-102731449-A 优先权日:2011-04-01 标题 :A kind of synthesis technology of dalfinacin intermediate 5-(2-bromoethyl)-2,3-dihydro-1-benzofuran
专利号:CN-102731449-B 优先权日:2011-04-01 标 题 :A kind of synthesis technology of dalfinacin intermediate 5-(2-bromoethyl)-2,3-dihydro-1-benzofuran
参考标题:Diversity‐oriented Synthesis Of Aliphatic Fluorides Via Reductive C(Sp3)−c(Sp3) Cross‐coupling Fluoroalkylation 作者:Jie Sheng,Hui‐qi Ni,Shan‐xiu Ni,Yan He,Ru Cui,Guang‐xu Liao,Kang‐jie Bian,Bing‐bing Wu,Xi‐sheng Wang |发布日期:2021.6.25 摘要:Catalyst And Alkyl Bromide Whereas The Generation Of Monofluoroalkyl Radical Is Not Involved In The Rate-Determining Step. This Strategy Provides A General And Efficient Method For The Synthesis Of Aliphatic Fluorides.