871728-33-5Relevant articles and documents
General strategy for large-scale synthesis of (+)-rivastigmine and (+)-NPS R-568
Rao, Ramakrishna,Shewalkar, Mukesh Padmakar,Nandipati, Ramadevi,Yadav, Jhillu Singh,Khagga, Mukkanti,Shinde, Devanand Baburao
experimental part, p. 589 - 598 (2011/11/29)
An economically viable strategy for the total synthesis of (+)-rivastigmine and (+)-NPS R-568 has been reported. The strategy involves regioselective hydrogenation of diastereomerically pure bis amine to realize the desired a-methyl chiral substituted benzyl amine. The route is economical, scalable, and versatile enough to be adapted to similar classes of compounds. Taylor & Francis Group, LLC.