Unusual formation of novel highly substituted N-(3-indolyl)-imidazoles
-
Add time:07/14/2019 Source:sciencedirect.com
Treatment of 3-amidoindoles with phosphoryl chloride leads to a dimerization of the resulting iminochlorides to form tetrasubstituted imidazoles in moderate yield. One indole ring undergoes ring-opening to allow the formation of the imidazole ring. This strategically simple synthesis considerably expands the scope of delivering N-indolylimidazoles.
We also recommend Trading Suppliers and Manufacturers of N-(3-bromophenyl)-N-(3-(3-bromophenyl)-4-(4-methoxyphenyl)-1,3-thiazol-2(3H)-ylidene)amine (cas 385397-80-8). Pls Click Website Link as below: cas 385397-80-8 suppliers
Prev:Amberlite IRA-400 Cl resin catalyzed synthesis of secondary amines and transformation into N-((1H-indol-3-yl) (heteroaryl) methyl)-N-heteroaryl benzenamines and bis-indoles via multicomponent reaction
Next:Sulfonated graphene oxide-catalyzed N-acetylation of amines with acetonitrile under sonication) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- An efficient and green synthesis of highly functionalized N-methyl-2-nitro-aryl-1H-benzo[f]chromen-3-amine derivatives under catalyst-free conditions07/17/2019
- One-pot and regioselective synthesis of polysubstituted 3,4-dihydroquinazolines and 4,5-dihydro-3H-1,4-benzodiazepin-3-ones by sequential Ugi/Staudinger/aza-Wittig reaction07/16/2019
- Sulfonated graphene oxide-catalyzed N-acetylation of amines with acetonitrile under sonication07/15/2019
- Amberlite IRA-400 Cl resin catalyzed synthesis of secondary amines and transformation into N-((1H-indol-3-yl) (heteroaryl) methyl)-N-heteroaryl benzenamines and bis-indoles via multicomponent reaction07/13/2019
- Ultrasonic promoted catalyst-free N-formylation of amines in neutral ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate07/12/2019
- Sulfur, selenium and tellurium containing amines act as effective carbonic anhydrase activators07/11/2019


