𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Optimized Procedure for the Cross-Aldol Condensation of Reactive Aldehydes

✍ Scribed by Boris, ; Kohler, A. B.


Book ID
121195038
Publisher
Taylor and Francis Group
Year
1985
Tongue
English
Weight
110 KB
Volume
15
Category
Article
ISSN
0039-7911

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Ketene bis(trimethylsilyl) acetals. Cros
✍ Jacques-Emile Dubois; Georges Axiotis; Emmanuel Bertounesque πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 French βš– 270 KB

enolsilanes 1 does not govern the stereochemistry of aldol condensation products. We recently reported for the first time', acetals la6'8, that compounds 2, structural analogous of add to aldehydes and Schiff bases in a cross-aldol type condensation, to afford B-hydroxyacids and B-Lactams respective

A convenient catalytic procedure for the
✍ Margherita De Rosa; Maria Rosaria Acocella; Rosaria Villano; Annunziata Soriente πŸ“‚ Article πŸ“… 2003 πŸ› Elsevier Science 🌐 English βš– 199 KB

In the presence of catalytic amount of chiral Ti(OiPr) 4 /BINOL (0.08 equiv.) the asymmetric aldol condensation of 6-methyl-4H-[1,3]-dioxin-4-one-derived silyloxydienes takes place in high yields and enantiomeric excesses with aromatic, heteroaromatic, unsaturated and aliphatic aldehydes. Notable am