An Experimental and Theoretical Study on the Unexpected Catalytic Activity of Triethanolamine for the Carboxylative Cyclization of Propargylic Amines with CO2. Issue 9 (11th April 2017)
- Record Type:
- Journal Article
- Title:
- An Experimental and Theoretical Study on the Unexpected Catalytic Activity of Triethanolamine for the Carboxylative Cyclization of Propargylic Amines with CO2. Issue 9 (11th April 2017)
- Main Title:
- An Experimental and Theoretical Study on the Unexpected Catalytic Activity of Triethanolamine for the Carboxylative Cyclization of Propargylic Amines with CO2
- Authors:
- Zhao, Yuling
Qiu, Jikuan
Li, Zhiyong
Wang, Huiyong
Fan, Maohong
Wang, Jianji - Abstract:
- Abstract: Chemical conversion of CO2 under atmospheric pressure and metal‐free conditions remains a great challenge. In this work, a series of alkanolamines, low‐cost and biodegradable bases, were used to catalyze the carboxylative cyclization of propargylic amines with CO2 . Among these alkanolamines, triethanolamine (TEOA) was found to be a highly efficient organocatalyst for this important transformation at atmospheric pressure, and a series of desired products were synthesized in good to excellent yields. After the reactions, TEOA could be easily recovered and reused without obvious reduction in the efficiency. DFT studies revealed that TEOA may activate CO2 to form a ring‐shaped carbonate intermediate that plays an important role in the catalysis of the reaction. This finding provides an effective and environmentally friendly alternative route for the production of 2‐oxazolidinones. Abstract : Tales of the unexpected : A series of alkanolamines, low‐cost and biodegradable bases, were used to catalyze the carboxylative cyclization of propargylic amines with CO2 . Triethanolamine (TEOA) was found to be a highly efficient organocatalyst for this important transformation at atmospheric pressure and a series of desired 2‐oxazolidinone products were synthesized in good to excellent yields.
- Is Part Of:
- ChemSusChem. Volume 10:Issue 9(2017)
- Journal:
- ChemSusChem
- Issue:
- Volume 10:Issue 9(2017)
- Issue Display:
- Volume 10, Issue 9 (2017)
- Year:
- 2017
- Volume:
- 10
- Issue:
- 9
- Issue Sort Value:
- 2017-0010-0009-0000
- Page Start:
- 2001
- Page End:
- 2007
- Publication Date:
- 2017-04-11
- Subjects:
- alkanolamines -- CO2 conversion -- density functional calculations -- heterocycles -- organocatalysis
Green chemistry -- Periodicals
Sustainable engineering -- Periodicals
Chemistry -- Periodicals
Chemical engineering -- Periodicals
660 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291864-564X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cssc.201700241 ↗
- Languages:
- English
- ISSNs:
- 1864-5631
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3133.482500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14245.xml