𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Three component reactions of N-nucleophiles and activated acetylenes with NH-acids: A facile synthesis in water

✍ Scribed by Faramarz Rostami Charati; Zinatossadat Hossaini; Mohammad R. Hosseini-Tabatabaei


Publisher
Journal of Heterocyclic Chemistry
Year
2011
Tongue
English
Weight
450 KB
Volume
49
Category
Article
ISSN
0022-152X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

A straightforward and efficient method for the synthesis of 1,2‐dihydroisoquinolines via a one‐pot, three‐component reaction of isoquinoline, activated acetylenes, and NH‐acids in water at 70°C without using any catalyst is reported. The method offers several advantages including high yields of products and an easy workup procedure. J. Heterocyclic Chem., (2012).


📜 SIMILAR VOLUMES


The reaction of (N-isocyanimino) triphen
✍ Ali Ramazani; Yavar Ahmadi; Morteza Rouhani; Nahid Shajari; Ali Souldozi 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 169 KB 👁 1 views

## Abstract Reactions of electron‐poor α‐haloketones with (__N__‐isocyanimino) triphenylphosphorane in the presence of aromatic carboxylic acids proceed smoothly at room temperature and in neutral conditions to afford disubstituted 1,3,4‐oxadiazole derivatives in high yields. © 2010 Wiley Periodica

Three-Component Reaction of an Isocyanid
✍ Ali Ramazani; Aram Rezaei; Amir Tofangchi Mahyari; Morteza Rouhani; Mehdi Khoobi 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 German ⚖ 138 KB 👁 1 views

The zwitterion, formed from the reaction of an alkyl isocyanide and a dialkyl acetylenedicarboxylate, reacts with phenacyl halides in H 2 O to produce g-iminolactone derivatives in high yields. H 2 O helps to avoid the use of highly toxic and environmentally unfavorable solvents for this conversion.