Rare earth perchlorate catalyzed glycosidation of glycosyl fluorides with trimethylsilyl ethers

ChemInform Abstract: Rare Earth Salts Pr

ChemInform Abstract: Rare Earth Salts Promoted Glycosidation of Glycosyl Fluorides.

✍ W.-S. KIM; S. HOSONO; H. SASAI; M. SHIBASAKI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

A New Glycosidation Procedure Utilizing

A New Glycosidation Procedure Utilizing Rare Earth Salts and Glycosyl Fluorides, with or without the Requirement of Lewis Acids

✍ Hosono, Shigeru; Kim, Won-Sup; Sasai, Hiroaki; Shibasaki, Masakatsu 📂 Article 📅 1995 🏛 American Chemical Society 🌐 English ⚖ 297 KB

A novel procedure for C-glycosylation in

A novel procedure for C-glycosylation involving Lewis acid-catalyzed coupling-reactions of glycosyl fluorides with enol trimethylsilyl ethers

✍ Younosuke Araki; Kazuko Watanabe; Fu-Hua Kuan; Kiyotaka Itoh; Naoki Kobayashi; Y 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 409 KB

ChemInform Abstract: A New Glycosylation

ChemInform Abstract: A New Glycosylation Procedure Utilizing Rare Earth Salts and Glycosyl Fluorides, With or Without the Requirement of Lewis Acids.

✍ S. HOSONO; W.-S. KIM; H. SASAI; M. SHIBASAKI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB

Pd-Catalyzed α-Arylation of Trimethylsil

Pd-Catalyzed α-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives

✍ Weiping Su; Steven Raders; John G. Verkade; Xuebin Liao; John F. Hartwig 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 1 views

Ketone enolates are among the most common nucleophiles in organic chemistry, and transition-metal-catalyzed cross-coup ling reactions are among the most commonly used catalytic processes. [1] However, the combination of these two chemistries-cross-coupling of enolate nucleophiles-has been developed

Pd-Catalyzed α-Arylation of Trimethylsil

Pd-Catalyzed α-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives

✍ Weiping Su; Steven Raders; John G. Verkade; Xuebin Liao; John F. Hartwig 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 1 views

Ketone enolates are among the most common nucleophiles in organic chemistry, and transition-metal-catalyzed cross-coup ling reactions are among the most commonly used catalytic processes. [1] However, the combination of these two chemistries-cross-coupling of enolate nucleophiles-has been developed