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High pressure activation in the asymmetric Michael addition of chiral imines to alkyl and aryl crotonates

✍ Scribed by Cheikhou Camara; Delphine Joseph; Françoise Dumas; Jean d'Angelo; Angèle Chiaroni


Book ID
104250481
Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
116 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


High pressure-mediated Michael addition of chiral imines derived from 2-methylcyclopentanone, 2-methylcyclohexanone and optically active 1-phenylethylamine, to methyl and phenyl crotonates was investigated. The corresponding adducts were obtained in fair yields and with a high degree of regio-, diastereo-and enantioselectivity.


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