α,ω-Halohydrins and Ω-acetylenic alcohols are protected as t-butyl ethers by reaction with isobutene and an acid catalyst : Amberlyst H-15. t-Butyl ethers are, in turn, cleaved to acetates by Ac2O and 10% FeCl3 in Et2O solvent. Under these mild conditions conjugated dienic systems are neither destroyed nor isomerized
The most common method for the deprotection ofTBDMS ethers utilizes stoichiometric amounts of tetrab...
1.Introduction 2.Hydroxy Protecting Groups 2.1. Esters 2.1.1. Protection 2.1.2. Deprotection 2....
Trityl ethers are chemoselectively deprotected to the corresponding alcohols in high yields by a cat...
In the past few years, metal perchlorates have been widely exploited as Lewis acid promoters in vari...
none7Abstract: The tert-butoxy derivative is one of the most underused alcohol protectingg roups. A...
A mild, efficient, and environmentally friendly method for the selective protection of secondary hyd...
4-Methoxyphenylmethyl ethers are widely utilized as alcohol protecting groups. FeCl<sub>3</sub> effe...
APPLICATIONS OF PERCHLORATES IN ORGANIC SYNTHESIS. A NEW AND GENERAL ROUTE TO t-BUTYL ETHERS Gius...
A protecting group that can be introduced efficiently without the need for any acid or base catalysi...
Benzyltriethylammonium tetrathiomolybdate, [PhCH2NEt3](2)MoS4, 1 deprotects propargyl ethers of alco...
[[abstract]]A series of β-(trimethylsilyl)ethoxymethyl ethers were hydrolyzed to their corresponding...
The reaction between alcohols and Boc2O leads to the formation of tert-butyl ethers and/or Boc-alcoh...
An efficient and highly chemoselective method fo the protection of free hydroxy compounds with 3,4-...
<div><p></p><p>The efficient deprotection of several acetals, dithioacetals, and tetrahydropyranyl (...
Alcohols are a common form of functionality in organic chemistry, and are often present in biologica...
The most common method for the deprotection ofTBDMS ethers utilizes stoichiometric amounts of tetrab...
1.Introduction 2.Hydroxy Protecting Groups 2.1. Esters 2.1.1. Protection 2.1.2. Deprotection 2....
Trityl ethers are chemoselectively deprotected to the corresponding alcohols in high yields by a cat...
In the past few years, metal perchlorates have been widely exploited as Lewis acid promoters in vari...
none7Abstract: The tert-butoxy derivative is one of the most underused alcohol protectingg roups. A...
A mild, efficient, and environmentally friendly method for the selective protection of secondary hyd...
4-Methoxyphenylmethyl ethers are widely utilized as alcohol protecting groups. FeCl<sub>3</sub> effe...
APPLICATIONS OF PERCHLORATES IN ORGANIC SYNTHESIS. A NEW AND GENERAL ROUTE TO t-BUTYL ETHERS Gius...
A protecting group that can be introduced efficiently without the need for any acid or base catalysi...
Benzyltriethylammonium tetrathiomolybdate, [PhCH2NEt3](2)MoS4, 1 deprotects propargyl ethers of alco...
[[abstract]]A series of β-(trimethylsilyl)ethoxymethyl ethers were hydrolyzed to their corresponding...
The reaction between alcohols and Boc2O leads to the formation of tert-butyl ethers and/or Boc-alcoh...
An efficient and highly chemoselective method fo the protection of free hydroxy compounds with 3,4-...
<div><p></p><p>The efficient deprotection of several acetals, dithioacetals, and tetrahydropyranyl (...
Alcohols are a common form of functionality in organic chemistry, and are often present in biologica...
The most common method for the deprotection ofTBDMS ethers utilizes stoichiometric amounts of tetrab...
1.Introduction 2.Hydroxy Protecting Groups 2.1. Esters 2.1.1. Protection 2.1.2. Deprotection 2....
Trityl ethers are chemoselectively deprotected to the corresponding alcohols in high yields by a cat...