Intramolecular Cycloaddition of Imines of Cysteine Derivatives
Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield
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| Other Authors: | , |
| Format: | article |
| Language: | eng |
| Published: |
1998
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| Subjects: | |
| Online Access: | http://hdl.handle.net/10316/13018 |
| Country: | Portugal |
| Oai: | oai:estudogeral.sib.uc.pt:10316/13018 |
| Summary: | Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield |
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