Highly Diastereoselective Vinylogous Mukaiyama Aldol Reaction of Isatins with 2-(Trimethylsilyloxy)furans Catalyzed by Quinine
Author:
Affiliation:
1. a State Key Laboratory and Institute of Elemento-Organic Chemistry , Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University , Tianjin , China
2. b Tianjin Yaohua High School , Tianjin , China
Funder
We thank the National Natural Science Foundation of China (21072102), the Committee of Science and Technology of Tianjin (11JCYBJC04200), and the State Key Laboratory of Elemento-organic Chemistry in Nankai University for financial support.
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2013.837926
Reference10 articles.
1. The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver
2. Recent advances in the chemistry of unsaturated lactones
3. Regioselective Functionalisation of the Da,b-Butenolide Ring via Group IV-B Organometallics
4. Recent Advances in Vinylogous Aldol Reactions and Their Applications in the Syntheses of Natural Products
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