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Lewis Acid Promoted Cyclocondensations of α-Ketophosphonoenoates with Dienes — From Diels—Alder to hetero Diels—Alder Reactions.

✍ Scribed by Stephen Hanessian; Philippe Compain


Publisher
John Wiley and Sons
Year
2010
Weight
36 KB
Volume
33
Category
Article
ISSN
0931-7597

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✦ Synopsis


Abstract

For Abstract see ChemInform Abstract in Full Text.


📜 SIMILAR VOLUMES


Enantioselective sequential transformati
✍ Dr. Lutz F. Tietze; Peter Saling 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 210 KB

Enantioselective reaction of the aldehydes la-g and the 1,3-dicarbonyl compound 2 in the presence of the chiral Lewis acid 5, derived from diacetone glucose, leads in a sequential transformation consisting of a Knoevenagel condensation and an intramolecular Diels Alder reaction to the cycloadducts 4