✦ LIBER ✦

Ionic Liquids with a Twist: New Routes to Liquid Salts

✍ Scribed by Ralf Giernoth

Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 218 KB
Volume: 49
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.201002393

No coin nor oath required. For personal study only.

✦ Synopsis

R.G. thanks the German Science Foundation (DFG) for funding through the Emmy Noether program and the special priority programs 1166 and 1191.

📜 SIMILAR VOLUMES

ChemInform Abstract: Ionic Liquids with

ChemInform Abstract: Ionic Liquids with a Twist: New Routes to Liquid Salts

✍ Ralf Giernoth 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 14 KB 👁 1 views

Ionic Liquid-based Synthesis—A Low-Tempe

Ionic Liquid-based Synthesis—A Low-Temperature Route to Nanophosphates

✍ Dr. Joanna Cybinska; Chantal Lorbeer; Prof. Dr. Eugeniusz Zych; Prof. Dr. Anja 📂 Article 📅 2011 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 340 KB

A New Generation of Ionic Liquids, Condu

A New Generation of Ionic Liquids, Conducting Salts & Strong Bronsted Acids

✍ Nikolai V. Ignat'ev; Urs Welz-Biermann 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 8 KB 👁 1 views

New Quaternary Polyfluoroalkyl-1,2,4-tri

New Quaternary Polyfluoroalkyl-1,2,4-triazolium Salts Leading to Ionic Liquids.

✍ Yousef R. Mirzaei; Jean'ne M. Shreeve 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 120 KB 👁 1 views

Mitsunobu Alkylation of Imidazole: A Con

Mitsunobu Alkylation of Imidazole: A Convenient Route to Chiral Ionic Liquids.

✍ Eun Jin Kim; Soo Y. Ko; Edward K. Dziadulewicz 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 19 KB 👁 1 views

Multicomponent reactions in chiral ionic

Multicomponent reactions in chiral ionic liquids: A stereocontrolled route to mercaptopyranothiazoles

✍ Lal Dhar S. Yadav; Beerendra S. Yadav; Vijai K. Rai 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 325 KB

## Abstract magnified image A low hazardous, one‐pot, expeditious annulation involving tandem Knoevenagel, Michael and ring transformation reactions of 3‐arylrhodanines, aromatic aldehydes and a mercaptoacetyl transfer agent, 2‐methyl‐2‐phenyl‐1,3‐oxathiolan‐5‐one, diastereoselectively yields 6‐me