Zeng Wang; Zihang Yuan; Xiaoyan Han; Zhiqiang Weng
Index: 10.1002/adsc.201800275
Full Text: HTML
An aluminium chloride‐mediated cascade reaction between pyrrolidones and trifluoroacetic anhydride is reported. Functionally diverse 1‐chloro‐2,2,2‐trifluoroethylidene‐substituted pyrrolidones were obtained in moderate to high yields through electrophilic trifluoroacetylation, nucleophilic chlorination, and elimination. This procedure has a wide scope, good functional‐group tolerance and the reaction conditions are amenable to scale up. Additionally the obtained 1‐chloro‐2,2,2‐trifluoroethylidene products can be applied to further functionalization as trifluoromethyl‐containing building blocks. Some of the title compounds showed fungicidal activity against cucumber downy mildew (CDM).
Iridium‐Catalyzed Tandem Cyclization of Benzoylacetonitriles...
2018-04-19 [10.1002/adsc.201800149] |
An Industrial Perspective on Counter Anions in Gold Catalysi...
2018-04-19 [10.1002/adsc.201800233] |
DBU‐Catalyzed [3+3] and [3+2] Annulation Reactions of Azomet...
2018-04-18 [10.1002/adsc.201800030] |
One‐pot Construction of Difluorinated Pyrrolizidine and Indo...
2018-04-18 [10.1002/adsc.201701643] |
Rhodium‐Catalyzed Chemo‐ and Enantioselective Hydrogenation ...
2018-04-17 [10.1002/adsc.201800243] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved