Ionic-Liquid-Mediated MacMillan’s Catalyst for Diels-Alder Reaction
Ionic liquids were used to enhance as well as recycle the MacMillan's catalyst 1 for the Diels-Alder reaction. Using our developed protocol, Diels-Alder adducts were obtained in good yields and selectivities along the 6 times recycling of MacMillan's imidazolidinone catalyst 1. Synthesis o...
Saved in:
Main Author: | Vivek Srivastava |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2013-01-01
|
Series: | Journal of Chemistry |
Online Access: | http://dx.doi.org/10.1155/2013/954094 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Diels–Alder Reaction as a Tool to Modify the Surface of Polymeric Microspheres
by: Marta Grochowicz, et al.
Published: (2015-08-01) -
Jean Arnold and Lila Marz Harper (eds), George Eliot. Interdisciplinary Essays. A Bicentennial Collection. Palgrave MacMillan, 2019
by: Sylvie Jougan
Published: (2021-11-01) -
DFT Investigation of the Stereoselectivity of the Lewis-Acid-Catalyzed Diels–Alder Reaction between 2,5-Dimethylfuran and Acrolein
by: Mohamed Chellegui, et al.
Published: (2025-01-01) -
T3P- A Novel Catalyst for Aza-Diels-Alder Reaction: One-Pot Synthesis of Pyrano[3,2-c]quinolines and furano[3,2-c]quinolines
by: T. S. R. Prasanna, et al.
Published: (2011-01-01) -
Substituent Effects on Regioselectivity of the Diels-Alder Reactions: Reactions of 10-Allyl-1,8-dichloroanthracene with 2-Chloroacrylonitrile, 1-Cyanovinyl Acetate and Phenyl Vinyl Sulfone
by: Mujeeb A. Sultan, et al.
Published: (2016-01-01)