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Enantioselective approach to butenolides upon reduction of alkoxycarbene complexes of chromium with chiral dihydropyridines

✍ Scribed by Henri Rudler; Andrée Parlier; Victor Certal; Jean-Cedric Frison


Book ID
104231058
Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
88 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis


Chromium alkoxycarbene complexes tethered to a triple bond react with a series of chiral dihydropyridines, among which is N-methyl-1,2-dihydronicotine, to give enantioselectively, upon cascade insertion reactions, polycyclic butenolides.


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Reaction of nucleophiles with alkoxycarb
✍ Henri Rudler; Andrée Parlier; Victor Certal; Nadège Humbert; Jacqueline Vaisserm 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 58 KB

A series of new substituted butenolides has been obtained either by reacting alkynylalkoxycarbene complexes 3 with simple nucleophiles such as metal hydrides, metal alkoxides and metal alkyls, or by reacting simple alkoxycarbene complexes 6 with more elaborate nucleophiles such as metal alkynolates