Diastereoselectivity in the Aza-Michael Reaction of Chiral α-Methylbenzylamines with α,β-Unsaturated Carbonyl Compounds
Abstract The aza-Michael reaction of (S)-(–)- and (R)-(+)-α-methylbenzylamines with trans-cinnamaldehyde and other α,β-unsaturated carbonyl compounds occurs with 52–98% diastereoselectivity (de); however, in the reaction with crotonaldehyde, the de is lower (20–38%). In the products obtained from th...
| المؤلفون الرئيسيون: | , , , |
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| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Georg Thieme Verlag KG
2018-04-01
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| سلاسل: | SynOpen |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1591999 |