Some scientific research about 142-25-6

If you are interested in 142-25-6, you can contact me at any time and look forward to more communication. Application In Synthesis of N1,N1,N2-Trimethylethane-1,2-diamine.

In an article, author is Hattori, Masashi, once mentioned the application of 142-25-6, Application In Synthesis of N1,N1,N2-Trimethylethane-1,2-diamine, Name is N1,N1,N2-Trimethylethane-1,2-diamine, molecular formula is C5H14N2, molecular weight is 102.18, MDL number is MFCD00014874, category is amides-buliding-blocks. Now introduce a scientific discovery about this category.

The catalytic enantioselective synthesis of the chiral key intermediate of the antidepressant (-)-paroxetine is demonstrated as a continuous flow process on multi-gram scale. The critical step is a solvent-free organocatalytic conjugate addition followed by a telescoped reductive amination-lactamization-amide/ester reduction sequence. Due to the efficient heterogeneous catalysts and the solvent-free or highly concentrated conditions applied, the flow method offers key advances in terms of productivity and sustainability compared to earlier batch approaches.

If you are interested in 142-25-6, you can contact me at any time and look forward to more communication. Application In Synthesis of N1,N1,N2-Trimethylethane-1,2-diamine.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics