546108-61-6Relevant articles and documents
Manganese-Catalyzed Direct Conversion of Ester to Amide with Liberation of H2
Mondal, Akash,Subaramanian, Murugan,Nandakumar, Avanashiappan,Balaraman, Ekambaram
supporting information, p. 3381 - 3384 (2018/06/11)
A simple and efficient Mn-catalyzed acylation of amines is achieved using both acyl and alkoxy functions of unactivated esters with the liberation of molecular hydrogen as a sole byproduct. The present protocol provides an atom-economical and sustainable route for the synthesis of amides from esters by employing an earth-abundant manganese salt and inexpensive phosphine-free tridentate ligand.
Synthesis of cyclic imides from simple diols
Zhang, Jian,Senthilkumar, Muthaiah,Ghosh, Subhash Chandra,Hong, Soon Hyeok
supporting information; experimental part, p. 6391 - 6395 (2010/11/05)
There's something imide so strong: Cyclic imides were synthesized from simple diols with primary amines in a single step using an in-situ-generated ruthenium catalytic system. The atom-economical and operatively simple syntheses of succinimides, phthalimides, and glutarimides, which are important building blocks in natural products and drugs, was also demonstrated. Copyright