𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Self-Promoted Aldol Reaction Between Aldehyde Having Lewis Base Moiety and Trimethylsilyl Enolate.

✍ Scribed by Takashi Nakagawa; Hidehiko Fujisawa; Teruaki Mukaiyama

Publisher
John Wiley and Sons
Year
2004
Weight
158 KB
Volume
35
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Product-Catalyzed Aldol Reaction between
Product-Catalyzed Aldol Reaction between Trimethylsilyl Enolates and Aldehydes
✍ Hidehiko Fujisawa; Takashi Nakagawa; Teruaki Mukaiyama πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 240 KB πŸ‘ 1 views

## Abstract Aldol reactions between trimethylsilyl ketene acetals and aldehydes by using a catalytic amount of alkoxide anion proceeded smoothly to afford the corresponding aldols in DMF, indicating that the initially‐formed aldolate anion effectively worked to catalyze the reaction. The β€œproduct‐c