This submission belongs to the session a. General Organic Synthesis of the event The 13th International Electronic Conference on Synthetic Organic Chemistry
Published date
31 Oct, 2009
Citation
Walid Fathalla, Ibrahim A. I. Ali, Synthesis of N-substituted-3,4,5,6-tetrachlorophthalimide using trichloroacetimidate C-C bond formation method, in Proceedings of The 13th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2009, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-13-00180
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Synthesis of N-substituted-3,4,5,6-tetrachlorophthalimide using trichloroacetimidate C-C bond formation method
Walid Fathalla 1
Ibrahim A. I. Ali 2
1. Department of Mathematics and Physical Sciences, Faculty of Engineering, Suez Canal University, Port Said, Egypt
2. Department of Chemistry, Faculty of Science, Suez Canal University, Ismailia, Egypt
Abstract
A series of N-substituted-3,4,5,6-tetrachlorophthalimides were prepared by a novel sequential reaction of trichloroacetimidate 3 with C-nucleophiles in the presence of TMSOTf. The nucleophiles include arenes, alkenes and active methylene to give the imidomethylation product of 3,4,5,6-tetrachlorophthalimide 5, 7, 9 and 11, respectively.
Keywords
Tetrachlorophthalimide
novel α-glucosidase inhibitors
trichloroacetimidate
C-C bond formation
C-nucleophiles
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