Extended knowledge of Oxazolidin-2-one

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of Oxazolidin-2-one, you can also check out more blogs about497-25-6

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Application In Synthesis of Oxazolidin-2-one. Introducing a new discovery about 497-25-6, Name is Oxazolidin-2-one

The Evans Aldol-Prins cyclization: A general and stereoselective method for the synthesis of 2,3,4,5,6-pentasubstituted tetrahydropyrans

A general and stereoselective method to synthesize 2,3,4,5,6-pentasubstituted tetrahydropyrans in three steps starting from three different aldehydes is described. Key substrates beta,gamma-unsaturated N-acyloxazolidin-2-ones were subjected to an “Evans Aldol-Prins” protocol to generate five sigma-bonds and five stereocenters in only a one-pot process with yields up to 60% and excellent stereoselectivities.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of Oxazolidin-2-one, you can also check out more blogs about497-25-6

Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H296NO – PubChem