Synthesis of bis(3-{[2-(allyloxy)ethoxy]methyl}-2,4,6-trimethylbenzoyl)(phenyl)phosphine oxide – a tailor-made photoinitiator for dental adhesives

• Norbert Moszner,
• Iris Lamparth,
• Jörg Angermann,
• Urs Karl Fischer,
• Frank Zeuner,
• Thorsten Bock,
• Robert Liska and
• Volker Rheinberger

Beilstein J. Org. Chem. 2010, 6, No. 26, doi:10.3762/bjoc.6.26

• photopolymerization of dimethacrylate resins, dental adhesives or composites and undergo an α-cleavage with the formation of benzoyl and germyl radicals, which may initiate the free-radical polymerization of the monomers present. In addition, bisacylphosphine oxides, such as commercially available bis(2,4,6

N-alkyl-N-(phosphonoethyl) substituted (meth)acrylamides – new adhesive monomers for self-etching self-priming one part dental adhesive

• Joachim E. Klee and
• Uwe Lehmann

Beilstein J. Org. Chem. 2009, 5, No. 72, doi:10.3762/bjoc.5.72

• oxide from BASF Interorgana. N,N′-diethyl-1,3-(bisacrylamido)propane, 3(4),8(9)-bis(acrylamidomethyl)tricyclo[5.2.1.02,6]decane all of Dentsply. Spectrum TPH (Dentsply) is a dental composite comprising methacrylate basing resins and glass filler. Nupro (Dentsply) is a polishing paste. Conditioner 36

Asymmetric reactions in continuous flow

• Xiao Yin Mak,
• Paola Laurino and
• Peter H. Seeberger

Beilstein J. Org. Chem. 2009, 5, No. 19, doi:10.3762/bjoc.5.19

• drops during flow-through that can often be problematic with gel-type resins. The flexibility and ease for adjusting porosity, composition and shape of these materials is an additional advantage [37][38]. The monolith-supported chiral amino alcohol catalyst 29 has been developed for the enantioselective

A biphasic oxidation of alcohols to aldehydes and ketones using a simplified packed- bed microreactor

• Andrew Bogdan and
• D. Tyler McQuade

Beilstein J. Org. Chem. 2009, 5, No. 17, doi:10.3762/bjoc.5.17

• , leading to no disruptions or degradation of the packing material. Thus, the AO-TEMPO resins are recyclable, showing no loss of catalytic activity and a substrate scope that encompasses many primary and secondary alcohols. The devices presented are predicted to be readily scaled-up to achieve the desired

Chemoselective reduction of aldehydes by ruthenium trichloride and resin- bound formates

• Basudeb Basu,
• Bablee Mandal,
• Sajal Das,
• Pralay Das and
• Ashis K. Nanda

Beilstein J. Org. Chem. 2008, 4, No. 53, doi:10.3762/bjoc.4.53

• ® resins; chemoselectivity; hydrogen transfer; reduction of carbonyl group; ruthenium chloride; Introduction Reduction of carbonyl functionality by transition metal-catalyzed transfer hydrogenation (CTH) with the aid of a suitable hydrogen donor is a valuable synthetic tool and has proved to be a viable

• ) and then the resins were filtered off by passing through a cotton bed. The filtrate was diluted with water, extracted with ether (2 × 10 mL) and the combined organic layers were washed with brine and dried over Na2SO4. Removal of the solvent afforded an oil, which was purified through a small pad of

Expedient syntheses of the N-heterocyclic carbene precursor imidazolium salts IPr·HCl, IMes·HCl and IXy·HCl

• Lukas Hintermann

Beilstein J. Org. Chem. 2007, 3, No. 22, doi:10.1186/1860-5397-3-22

• intermediates, producing brown resins. We reasoned that the water of condensation had to be removed either chemically or simply by homogeneous dissolution in the reaction mixture. Indeed, by adding 30% of tetrahydrofurane (THF) to the reaction solvent (entry 13), IXy·HCl (3) was precipitated in very high yield