✦ LIBER ✦

Montmorillonite K10 Catalyzed Nucleophilic Addition Reaction to Aldimines in Water.

✍ Scribed by Takahiko Akiyama; Keiichiro Matsuda; Kohei Fuchibe

Book ID: 101987429
Publisher: John Wiley and Sons
Year: 2006
Weight: 23 KB
Volume: 37
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200609040

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Montmorillonite-K10 Catalyzed Addition O

Montmorillonite-K10 Catalyzed Addition OF Trimethylsilylcyanide (TMSCN) to Aldehydes.

✍ Somanathan, R.; Rivero, I. A.; Gama, Angeles; Ochoa, A.; Aguirre, G. 📂 Article 📅 1998 🏛 Taylor and Francis Group 🌐 English ⚖ 234 KB

ChemInform Abstract: Montmorillonite-K10

ChemInform Abstract: Montmorillonite-K10 Catalyzed Addition of Trimethylsilylcyanide (TmsCN) to Aldehydes.

✍ R. SOMANATHAN; I. A. RIVERO; A. GAMA; A. OCHOA; G. AGUIRRE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

Clay montmorillonite K10 catalyzed aldol

Clay montmorillonite K10 catalyzed aldol-type reaction of aldehydes with silyl enol ethers in water

✍ Teck-Peng Loh; Xu-Ran Li 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 733 KB

Metal-Catalyzed Reactions in Water (Dixn

Metal-Catalyzed Reactions in Water (Dixneuf/Metal-Catalyzed Reactions in Water) || Catalytic Nucleophilic Additions of Alkynes in Water

✍ Dixneuf, Pierre H.; Cadierno, Victorio 📂 Article 📅 2013 🏛 Wiley-VCH Verlag GmbH & Co. KGaA ⚖ 188 KB

ChemInform Abstract: Clay Montmorillonit

ChemInform Abstract: Clay Montmorillonite K10 Catalyzed Aldol-Type Reaction of Aldehydes with Silyl Enol Ethers in Water.

✍ Teck-Peng Loh; Xu-Ran Li 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Double nucleophilic addition reaction to

Double nucleophilic addition reaction to α,β-unsaturated aldimines promoted by aluminum chloride and a limited amount of water

✍ Makoto Shimizu; Toshiki Ogawa; Takafumi Nishi 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 64 KB

In the presence of AlCl 3 and MS 4 A containing H 2 O, ketene silyl acetals underwent 1,4-and then 1,2-addition with a,b-unsaturated imines to give doubly alkylated products in good yields with high diastereomeric excesses.