Enantioselectivity investigation of short polar peptides with different positions in the Michael reaction
This work reports the effectiveness of short polar peptides as asymmetric catalysts in Michael reactions to attain good yields of enantio- and diastereoselective isomers. In a comparison, glutamic acid and histidine produced greater ee and yields when they were applied as the second amino acid in sh...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English English |
| Published: |
Taylor & Francis
2013
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| Online Access: | http://psasir.upm.edu.my/id/eprint/30274/1/Enantioselectivity%20investigation%20of%20short%20polar%20peptides%20with%20different%20positions%20in%20the%20Michael%20reaction.pdf |