CAS: 2268-17-9; 2,4,6-Trifluorophenol

上下游产品

2,4,6-trifluoroanisole 1,3,5-trifluorobenzene 2,4,6-trifluorophenylboronic acid (2,4,6-trifluoro-phenoxy)-acetic acid (S)-ethyl 1-(1-(tert-butyldimethylsilyloxy)-3-methylbutan-2-yl)-7-methoxy-4-oxo-6-((2,4,6-trifluorophenoxy)methyl)-1,4-dihydro-1,8-naphthyridine-3-carboxylate

2,4,6-三氟苯甲醚置于氢碘酸,乙酸酐体系中,化学反应生成2,4,6-三氟苯酚
参考文献:Aromatic Fluorine Compounds. Viii. Plant Growth Regulators And Intermediates1,2
标题:Aromatic Fluorine Compounds. Viii. Plant Growth Regulators And Intermediates1,2
摘要:
Doi:10.1021/ja01510A021

专利信息

专利号:WO-2025149479-A1
优先权日:2024-01-12
标题:Synthesis of modified nucleoside triphosphates
发明人：KUCHELMEISTER HANNES; PFAFFENEDER TONI; MEX MARTIN; VETH SIMON; MENKE JAN-MICHAEL
权利人:ROCHE DIAGNOSTICS GMBH
摘要:The invention relates to a new diastereoselective synthesis method for highly modified nucleoside triphosphates with two conjugable groups. The method works in liquid phase with conventional laboratory equipment as used in any chemical laboratory or production. For this, a new chiral P(V) phosphorylation reagent has been designed that allows highly efficient diastereoselective synthesis under mild conditions. Overall, a highly efficient, diastereoselective, high quality, cost-effective synthetic method of modified nucleoside triphosphates has been developed.

专利号:US-9533959-B2
优先权日:2013-10-07
标 题:Methods of regioselective synthesis of 2,4-disubstituted pyrimidines
发明人：CHARRIER JEAN-DAMIEN; O'DONNELL MICHAEL EDWARD
权利人:VERTEX PHARMA
摘要:The present invention relates to the novel regioselective syntheses of 2,4-disubstituted pyrimidines through sequential nucleophilic aromatic substitutions.

专利号:US-6828466-B2
优先权日:2002-07-19
标题:Process for the synthesis of phenols from arenes
发明人：MALECZKA JR ROBERT E; SMITH III MILTON R; HOLMES DANIEL; SHI FENG
权利人:UNIV MICHIGAN STATE
摘要:A process to synthesize substituted phenols such as those of the general formula RR'R''Ar(OH) wherein R, R', and R'' are each independently hydrogen or any group which does not interfere in the process for synthesizing the substituted phenol including, but not limited to, halo, alkyl, alkoxy, carboxylic ester, amine, amide; and Ar is any variety of aryl or hetroaryl by means of oxidation of substituted arylboronic esters is described. In particular, a metal-catalyzed C-H activation/borylation reaction is described, which when followed by direct oxidation in a single or separate reaction vessel affords phenols without the need for any intermediate manipulations. More particularly, a process wherein Ir-catalyzed borylation of arenes using pinacolborane (HBPin) followed by oxidation of the intermediate arylboronic ester by OXONE is described.

专利号:US-10005737-B2
优先权日:2013-10-07
标题:Methods of regioselective synthesis of 2,4-disubstituted pyrimidines

专利号:US-2015099875-A1
优先权日:2013-10-07
标题:Methods of regioselective synthesis of 2,4-disubstituted pyrimidines

专利号:US-2016159749-A1
优先权日:2013-10-07
标题 :Methods of regioselective synthesis of 2,4-disubstituted pyrimidines