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Schmidt Reaction (schmidt + reaction)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

5-Acyl-2H-pyran-2-ones in the Schmidt Reaction: Migration of the Pyran-2-one Ring.

CHEMINFORM, Issue 23 2007
Franc Pozgan
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source]

P2O5/SiO2 -Catalyzed One-Pot Synthesis of Amides from Ketones via Schmidt Reaction under Microwave Irradiation in Dry Media.

CHEMINFORM, Issue 45 2006
Hossein Eshghi
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source]

Gold(I)-Catalyzed Intramolecular Acetylenic Schmidt Reaction.

CHEMINFORM, Issue 50 2005
David J. Gorin
No abstract is available for this article. [source]

ChemInform Abstract: 3,6,6-Trimethyl-4-oxo-1-(2-pyridyl)-4,5,6,7-tetrahydroindazole (I) in Schmidt Reaction and Beckmann Rearrangement Conditions for the 4-Hydroxyimino Derivative (III).

CHEMINFORM, Issue 19 2001
L. G. Delyatitskaya
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

ChemInform Abstract: Azidomercurations of Alkenes: Mercury-Promoted Schmidt Reactions.

CHEMINFORM, Issue 16 2001
William H. Pearson
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Novel gel-entrapped base catalysts for the Claisen,Schmidt reaction

JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 7 2004
Sachin S Chaphekar
Abstract Novel gel-entrapped base catalysts (GEBCs) were prepared by entrapping aqueous solutions of bases in a gel matrix of agar agar. The bases used were NaOH, KOH, morpholine and piperidine. Ternary phase diagrams were constructed for the water,base,agar agar system to identify the various phases and especially the solid phase, useful as a solid base catalyst. The 10% NaOH solid gel was used to effect the Claisen,Schmidt reaction between benzaldehydes and acetophenones in ethanol under heterogeneous conditions to obtain 70,100% yield of the products. The solid GEBCs obtained using other bases were also used for the same reaction; however, the yields were lower. The catalyst needed no activation prior to use and could be recycled. Copyright © 2004 Society of Chemical Industry [source]