Stereoselective reduction of 1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione using sodium borohydride with selected metal chlorides
1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione is an intermediate product produced in the synthesis towards the natural bioactive compound, zopfiellamide A. This compound was synthesized via four main steps including dimethylations, addition with CuBr2, cyclization with benzylamine and react...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | en en |
| Published: |
Universiti Kebangsaan Malaysia (UKM)
2017
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| Subjects: | |
| Online Access: | http://irep.iium.edu.my/60337/1/NorSaliyana_21_5_22-2.pdf http://irep.iium.edu.my/60337/3/60337_Stereoselective%20reduction_scopus.pdf http://irep.iium.edu.my/60337/ |
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| Summary: | 1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione is an intermediate product produced in the synthesis towards the natural bioactive compound, zopfiellamide A. This compound was synthesized via four main steps including dimethylations, addition with CuBr2, cyclization with benzylamine and reaction with formaldehyde. The corresponding intermediate was an α,ß-unsaturated ketone having exo-alkene group, and it was subjected to reduction using sodium borohydride and selected metal chlorides. In this study, the effect and the hydride transfer mechanism of sodium borohydride-metal chlorides system in the reduction of 1-benzyl-3,3-dimethyl-5-methylenepyrrolidine-2,4-dione was investigated based on the stereochemical outcome of the product.
Keywords: stereoselective, reduction, metal borohydride, exo-alkene |
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