نتایج جستجو برای: fluoro β diketones

تعداد نتایج: 185255  

Journal: :Dalton transactions 2012
Christian Maurer Ernst Pittenauer Van An Du Günter Allmaier Ulrich Schubert

Reaction of Ti(OiPr)(4) with various bis(β-diketones) and bis(β-ketoesters) (LH(2)) results in the formation of dimeric complexes [Ti(OiPr)(2)L](2), where each metal centre is coordinated by two terminal OiPr ligands and two bridging β-diketonate or β-ketoesterate groups (L). Macrocycles containing two M(OiPr)(2) moieties are thus formed. Reaction of Zr(OiPr)(4) with the same bis(β-diketones) a...

Journal: :Organic & biomolecular chemistry 2011
Federico Berti Simone Bincoletto Ivan Donati Giampaolo Fontanive Massimo Fregonese Fabio Benedetti

The reduction of 1,3-diketones and β-hydroxyketones with NaBH(4) in aqueous acetonitrile is highly stereoselective in the presence of stoichiometric amounts of bovine or human albumin, giving anti 1,3-diols with d.e. up to 96%. The same reaction, without albumin, gives syn and anti 1,3-diols in approximately 1:1 ratio. The presence of an aromatic carbonyl group is essential for diastereoselecti...

Journal: :Inorganic chemistry 2016
Blenerhassitt E Buitendach Elizabeth Erasmus Marilé Landman J W Hans Niemantsverdriet Jannie C Swarts

Reaction of [Mn3(OAc)6O·3H2O](+) (1) with ferrocenyl β-diketones of the type FcCOCH2COR with R = CF3 (2a) and CH3 (2b), Ph = C6H5 (2c), and Fc = Fe(II)(η(5)-C5H4)(η(5)-C5H5) (2d) yielded a series of ferrocene-functionalized β-diketonato manganese(III) complexes 3a-3d, respectively, of general formula [Mn(FcCOCHCOR)3]. The mixed-ligand β-diketonato complex [Mn(FcCOCHCOFc)2(FcCOCHCOCH3)] (4) was ...

Journal: :Chemical and Pharmaceutical Bulletin 1960

2016
Andreas Steinbacher Pramod Kumar Verma Federico Koch Patrick Nuernberger Tobias Brixner

The photodynamics in symmetric and unsymmetric β-diketones are studied with transient absorption in the deep-UV. Excitation leads to ultrafast ESIPT while further relaxation and isomerization processes depend on the molecular symmetry and solvent environment. OCIS codes: (320.7150) Ultrafast spectroscopy; (300.6540) Spectroscopy, ultraviolet; (190.7110) Ultrafast nonlinear optics

Journal: :Organic & biomolecular chemistry 2014
Karuppusamy Sakthivel Kannupal Srinivasan

Indium(III) triflate is found to be an effective catalyst for the benzannulation reactions of o-alkynylbenzaldehydes with enolisable aldehydes, ketones, 1,3-diketones and β-keto esters. The reactions produce naphthyl ketones through ring opening of adducts arising from the inverse electron demand Diels-Alder reactions between in situ generated isochromenylium cations and enols. The main feature...

Journal: :Dalton transactions 2016
Bing Li Hongfeng Li Peng Chen Wenbin Sun Cheng Wang Ting Gao Pengfei Yan

Three neodymium complexes Nd(TTA)3(DMSO)2 (1, TTA = 2-thenoyltrifluoroacetone), Nd2(BDT)3(DMSO)6 (2, BDT = bis(4,4,4-trifluoro-1,3-dioxobutyl)thiophene) and Nd2(BTT)3(DMSO)4 (3, BTT = bis(4,4,4-trifluoro-1,3-dioxobutyl)(2,2'-bithiophene)) constructed from three thiophene-based β-diketonate ligands, were prepared for the purpose of building the relationships between the structures, energy levels...

2005
Gideon GROGAN

The enzymatic cleavage of C–C bonds in β-diketones is, comparatively, a little studied biochemical process, but one that has important relevance to human metabolism, bioremediation and preparative biocatalysis. In recent studies, four types of enzymes have come to light that cleave C–C bonds in the β-diketone functionality using different chemical mechanisms. OPH [oxidized poly(vinyl alcohol) h...

Journal: :Chemical communications 2015
Jorge Saavedra-Olavarría Gean C Arteaga Jhon J López Edwin G Pérez

A copper-catalyzed regio- and intermolecular aminofluorination of styrenes has been developed. In this reaction Ph-I=N-Ts and Et3N·3HF act as nitrogen and fluorine sources, respectively. The obtained β-fluoro-N-Ts-phenethylamines can be N-alkylated with subsequent deprotection affording the corresponding β-fluoro-N-alkylated phenethylamines, which are interesting building blocks for compounds a...

Journal: :Journal of Synthetic Organic Chemistry, Japan 1969

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