Interhalogen-catalyzed cleavages of ethers and esters with trimethylsilyl bromide or chloride

conversion of trimethylsilyl ethers to a

conversion of trimethylsilyl ethers to acetyl or formyl esters with TiCl 4

✍ Iranpoor, Nasser; Zeynizadeh, Behzad 📂 Article 📅 1999 🏛 Taylor and Francis Group 🌐 English ⚖ 201 KB

ChemInform Abstract: Conversion of Trime

ChemInform Abstract: Conversion of Trimethylsilyl Ethers to Acetyl or Formyl Esters with TiCl4.

✍ Nasser Iranpoor; Behzad Zeynizadeh 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

Palladium-catalyzed coupling reaction of

Palladium-catalyzed coupling reaction of amino acids (esters) with aryl bromides and chlorides

✍ Fangfang Ma; Xiaomin Xie; Lina Ding; Jinsheng Gao; Zhaoguo Zhang 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 452 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

Mild deprotection of methoxymethyl, meth

Mild deprotection of methoxymethyl, methylthiomethyl, methoxyethoxymethyl, and and β-(trimethylsilyl,)ethoxymethyl, esters with magnesium bromide in ether

✍ Sunggak Kim; Young Hee Park; In Seo Kee 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 133 KB