700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ ReadersThis Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
Original Articles Open Access
The reactions between oxyallyl cations and 9-substituted anthracene to obtain 9,10-dihydro-9,10- propanoanthracene substituted have not yet been studied extensively. For this reason, we used (4+3) cycloaddition reactions of 9-(4-pentenyl)-anthracene with 1,1,3,3-tetrabromoacetone as key step for preparation of a homologue of maprotiline which has been synthesized and developed into a clinically useful drug for the treatment of depressant by Ciba-Geigy research group in Switzerland.
To read the full article Peer-reviewed Article PDF
Author(s): Adel AlSaeedi Usama Karama Mujeeb A Sultan and Mazahar Farooquia
Oxyallyl Cations, (4+3) Cycloaddition Reactions, Homologue, Ludiomil, 1,1,3,3-Tetrabromoacetone, Bishomomaprotiline