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Enantioselective photodeconjugation of α,β-unsaturated esters in the presence of catalytic amounts of a chiral-inducing entity

✍ Scribed by Reza Mortezaei; Françoise Henin; Jacques Muzart; Jean-Pierre Pete


Book ID
108382649
Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
142 KB
Volume
26
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES


A very enantioselective photodeconjugati
✍ Olivier Piva; Françoise Henin; Jacques Muzart; Jean-Pierre Pete 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 213 KB

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