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A very enantioselective photodeconjugation of α,β-unsaturated esters

✍ Scribed by Olivier Piva; Françoise Henin; Jacques Muzart; Jean-Pierre Pete


Book ID
104227934
Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
213 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis


An enantiomeric excess up to 70% can be obtained in the photodeconjugation of conjugated esters in the presence of (1 R, 2s) I-phenyl, 2-isopropylamino-propanol.

It was shown previously that chiral b,y-unsaturated esters can be produced when conjugated


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