January 2000 - 16 articles
The use of an enantiomerically pure amino alcohol, coupled to a transfer hydrogenation process, in the asymmetric catalysis of the reduction of ketones to alcohols, is described. The process works well for unfunctionalised ketones, affording e.e.s of...
It is one of the great ironies of our information age that at the same time that we have the technical capability to make information freely available world-wide, budget problems are seriously endangering the free access to scientific information.[...]
The open source program for drawing 2D chemical structures JChemPaint, its current features, its envisioned further development and the principles enabling researchers and students at places all over the world to collaboratively develop such a progra...
A stepwise synthesis of a-unsubstituted pyrroles with desired substituents in the b-positions of the ring has been devised.
Furylcyclohexanones can be prepared by the reaction of acetoacetic ester (AAE) with b-furyl-a,b-unsaturated ketones [1,2].[...]
It is known that indazoles have varied biological activity [1,2].[...]
The general part of the experimental section and the purposes of this synthesis have been present elsewhere [1].[...]
Adenine (1, 0.676 g, 5.0 mmol) was suspended in anhydrous DMF (20 mL) and sodium hydride (55-60 % suspension in mineral oil, 0.262 g, 6.0 mmol) was added at room temperature.[...]
Methanediphosphonic acid tetraethyl ester is a useful intermedaite for the synthesis of phosphonoalkenes [1] or diphosphonoalkenes [2].[...]
The starting 4-hydroxy-6-methyl-1-phenethyl-2(1H)-pyridinone (1) was prepared according to the known procedure [1,2].[...]
of 2
Get Alerted
Add your email address to receive forthcoming issues of this journal.
