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Mannich-Type Reactions Catalyzed by Neutral Salts in Water

✍ Scribed by Catherine Loncaric; Kei Manabe; Shū Kobayashi


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
93 KB
Volume
345
Category
Article
ISSN
1615-4150

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✦ Synopsis


Abstract

Mannich‐type reactions of imines with silicon enolates were found to be catalyzed by neutral salts such as sodium triflate in water as a suspension medium. Unusual kinetic behavior indicates that the presence of the Mannich adduct facilitates the rate of its formation.


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Brønsted Acid-Catalyzed Mannich-Type Rea
✍ Takahiko Akiyama; Jun Takaya; Hirotaka Kagoshima 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 126 KB 👁 1 views

HBF 4 -catalyzed Mannich-type reaction of silyl enolates with aldimines took place smoothly in aqueous organic solvent to afford b-aminocarbonyl compounds in high yields. The HBF 4 -catalyzed Mannich-type reaction also proceeded smoothly in water without organic solvent in the presence of a surfacta