نتایج جستجو برای: fluorinated enones

تعداد نتایج: 4816  

2016
Stalin R Pathipati Angela van der Werf Lars Eriksson Nicklas Selander

A diastereoselective three-component reaction between alkynyl enones, aldehydes and secondary amines is reported. With the aid of a benign indium catalyst, a range of highly substituted cyclopenta[c]furan derivatives can be obtained in a single-step procedure. The formation of the stereodefined heterocyclic motifs takes place via in situ generation of enamines followed by two sequential cycliza...

2017
Ken Takaki Makoto Hino Akira Ohno Kimihiro Komeyama Hiroto Yoshida Hiroshi Fukuoka

Thiazolium carbene-catalyzed reactions of 1,2-diketones and 1,2,3-triketones with enones and ynones have been investigated. The diketones gave α,β-double acylation products via unique Breslow intermediates isolable as acid salts, whereas the triketones formed stable adducts with the NHC instead of the coupling products.

2017
Yasaman Delaviz Meilin Yang Paul Santerre

The monomeric components of resin composites in dental restorative materials are susceptible to hydrolysis in the oral cavity. The main objective of this study was to assess the bio-stability of fluorinated urethane dimethacrylates and determine the nature of fluoro-chemistry interactions with protein and bacterial adhesion (both sources of hydrolytic activity) onto cured resin. Degradation stu...

2001
Hans J. Reich James M. Renga

The scope and limitation of the transformation of ketones to enones by selenenylation followed by selenoxide elimination have been examined. Several procedures for the preparation of a-phenylseleno ketones have been developed. The most useful are direct selenenylation of ketone enolates using PhSeBr and the reaction of enol acetates with electrophilic selenium species such as benzeneselenenyl t...

Journal: :Journal of the American Chemical Society 2010
Samantha L Riches Chandreyee Saha Noelia Fontán Filgueira Emma Grange Eoghan M McGarrigle Varinder K Aggarwal

In this paper, we describe studies on the cyclopropanation of Michael acceptors with chiral sulfur ylides. It had previously been found that semi-stabilized sulfonium ylides (e.g., Ph-stabilized) reacted with cyclic and acyclic enones and substituted acrylates with high ee and that stabilized sulfonium ylides (e.g., ester-stabilized) reacted with cyclic enones again with high ee. The current st...

2011
Anca Gliga Bernd Goldfuss Jörg M Neudörfl

Fluorinated and nonfluorinated phosphonates are employed as precatalysts in lithium phosphonate catalyzed cross benzoin couplings. Surprisingly, a decreased catalytic activity for the fluorinated precatalysts compared to the nonfluorinated systems is observed. Furthermore, the ring size of six, seven and nine membered ring catalysts appears not to be crucial for their catalytic activity.

Journal: :Journal of oral rehabilitation 1996
T Li R G Craig

Fluorinated Bis-GMA was synthesized and used with other commercially available fluorinated monomers and diluents to prepare hydrophobic composites. The composites were formulated as one-paste systems and were polymerized using blue light. Mechanical properties and water-related qualities were determined. Fluorination generally improved the hydrophobicity of the composites, but there was no clea...

Journal: :Organic & biomolecular chemistry 2013
Emerson Giovanelli Lionel Moisan Sébastien Comesse Sébastien Leroux Bernard Rousseau Paul Hellier Marc Nicolas Eric Doris

The syntheses of 20,20-difluorocatharanthine and congeners, starting from the naturally occurring catharanthine, are reported. The fluorinated catharanthine analogues were investigated as potential precursors to dimeric Vinca alkaloids of the vinflunine family. However, the biomimetic coupling of the fluorinated catharanthine derivatives with vindoline led to unexpected alkaloid structures, the...

Journal: :Chemical communications 2013
Ran-Ning Guo Xian-Feng Cai Lei Shi Zhi-Shi Ye Mu-Wang Chen Yong-Gui Zhou

An efficient iridium-catalyzed asymmetric hydrogenation of the fluorinated isoquinoline derivatives has been successfully developed for the synthesis of chiral fluorinated tetrahydroisoquinoline derivatives with up to 93% ee. This methodology features the use of a hydrochloride salt as well as a catalytic amount of halogenated hydantoin which were vital for the reactivity, enantioselectivity, a...

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