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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| Outros Autores: | , |
| Formato: | article |
| Idioma: | eng |
| Publicado em: |
1998
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| Assuntos: | |
| Texto completo: | http://hdl.handle.net/10316/13018 |
| País: | Portugal |
| Oai: | oai:estudogeral.sib.uc.pt:10316/13018 |
| Resumo: | 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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