نتایج جستجو برای: epoxy compounds

تعداد نتایج: 239236  

2016
G. Trott P. K. Saini C. K. Williams

This article summarizes and reviews recent progress in the development of catalysts for the ring-opening copolymerization of carbon dioxide and epoxides. The copolymerization is an interesting method to add value to carbon dioxide, including from waste sources, and to reduce pollution associated with commodity polymer manufacture. The selection of the catalyst is of critical importance to contr...

Journal: :Organic letters 2007
Michelle M Rogers Vasily Kotov Jaruwan Chatwichien Shannon S Stahl

Palladium-catalyzed methods for intermolecular aerobic oxidative amination of alkenes have been identified that are compatible with the use of alkene as the limiting reagent. These procedures, which enhance the utility of this reaction with alkenes that are not commercially available, are demonstrated with substrates bearing dialkyl ether, carboxyester, epoxide, and silyl ether groups.

Journal: :Physical chemistry chemical physics : PCCP 2013
Alister J Page Chien-Pin Chou Buu Q Pham Henryk A Witek Stephan Irle Keiji Morokuma

We present a detailed analysis of the factors influencing the formation of epoxide and ether groups in graphene nanoflakes using conventional density functional theory (DFT), the density-functional tight-binding (DFTB) method, π-Hückel theory, and graph theoretical invariants. The relative thermodynamic stability associated with the chemisorption of oxygen atoms at various positions on hexagona...

Journal: :Journal of oleo science 2013
Manneganti Vijay Rachapudi Badari Narayana Prasad Bethala Lakshmi Anu Prabhavathi Devi

A convinent and efficient method was developed for the synthesis of 1,2-azidoalcohols by ring opening of terminal epoxides with sodium azide employing glycerol-based sulphonic acid functionalized carbon as heterogeneous catalyst in aqueous acetonitrile. The reaction is highly regioselective and affords the corresponding products in excellent yields (78-100%) under mild reaction conditions. The ...

Journal: :Organic & biomolecular chemistry 2005
Meritxell Egido-Gabás Pedro Serrano Josefina Casas Amadeu Llebaria Antonio Delgado

A series of 13 aminocyclitol derivatives belonging to two different families is described. Their configuration is governed by the regio- and stereocontrolled epoxide opening of a suitably protected conduritol-B epoxide. Studies on several glycosyl processing enzymes indicate that some of them are good inhibitors of glucosylceramide hydrolase. A rationale to account for preliminary structure-act...

2013
Venumadhav Janganati Narsimha Reddy Penthala Sean Parkin Peter A. Crooks

The title compound, C18H24N2O4·H2O {systematic name: (1aR,7aS,8R,10aS,10bS,E)-5-hy-droxy-methyl-8-[(1H-imidazol-1-yl)meth-yl]-1a-methyl-2,3,6,7,7a,8,10a,10b-octa-hydro-oxireno[2',3':9,10]cyclo-deca-[1,2-b]furan-9(1aH)-one monohydrate}, an imidazole derivative of melampomagnolide B was synthesized under Michael addition conditions. The mol-ecule is built up from fused ten-, five- (lactone) and t...

2001
Mauricio Gomes Constantino Valdemar Lacerda Valquiria Aragão

Epoxide ring opening is a frequently required transformation in Organic Synthesis. In this paper we describe the application of NbCl5 for this purpose using three different substrates. Chlorohydrins, 1,2-diols, products containing solvent residues as well as rearrangement products are obtained, depending on both the substrate structure and reaction conditions. Rationalizations to account for so...

2012
Zhe She Andrea DiFalco Georg Hähner Manfred Buck

Self-assembled monolayers (SAMs) of 4'-methylbiphenyl-4-thiol (MBP0) adsorbed on polycrystalline gold substrates served as templates to control electrochemical deposition of Cu structures from acidic solution, and enabled the subsequent lift-off of the metal structures by attachment to epoxy glue. By exploiting the negative-resist behaviour of MBP0, the SAM was patterned by means of electron-be...

Journal: :Organic & biomolecular chemistry 2011
Pipas Saha Paramartha Gogoi Anil K Saikia

An efficient methodology for the synthesis of oxabicyclo[3.3.1]nonenes and substituted tetrahydropyrans has been developed in moderate yields from the reaction of geraniol with aldehydes and epoxides promoted by boron trifluoride etherate.

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