Najwa Sbei, Belen Batanero, Fructuoso Barba, Beya Haouas, Mohamed Lamine Benkhoud, Isidoro Barba
Index: 10.1016/j.tet.2018.03.010
Full Text: HTML
A new series of 3,4-disubstituted quinazolin-2-ones, with potential T-type calcium channel antagonist activity, and new 4-methylene-quinazolin-2-ones, promising catalysts as N-heterocyclic olefins, have been prepared in good yield by a simple reaction between 2-aminobenzophenone, or 2-aminoacetophenone, and cyanomethyl anion electrogenerated by acetonitrile reduction at a graphite electrode, followed by the addition of different organic isocyanates and subsequent heterocyclization.
|
Synthesis of chiral α-amino anilides via a DMEDA-promoted se...
2018-04-11 [10.1016/j.tet.2018.03.003] |
|
A site isolation-enabled organocatalytic approach to enantio...
2018-04-11 [10.1016/j.tet.2018.04.022] |
|
Chemoselectivity in the Kosugi-Migita-Stille coupling of bro...
2018-04-10 [10.1016/j.tet.2018.02.051] |
|
Process design methodology for organometallic chemistry in c...
2018-04-07 [10.1016/j.tet.2018.04.020] |
|
Substrate engineering: Effects of different N-protecting gro...
2018-04-07 [10.1016/j.tet.2018.04.012] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2026 ChemSrc All Rights Reserved