A new procedure for the deprotection of carboxylic tert-butyl and 1-adamantyl esters, and N-Boc-amines using H2SO4 in CH2Cl2 is described. The proposed method is simple, cheap, eco-friendly and represents a valid alternative to existing ones, with special significance in large scale applications. 2005 Elsevier Ltd. All rights reserved
An efficient, environmentally benign, highly facile and convenient synthetic protocol for the select...
A series of competition experiments has revealed that selective cleavage of N-benzyl-protected secon...
It is shown that prop-2-ynyl esters are useful protecting groups for carboxylic acids and that they ...
A simple, efficient, and alternative method has been developed for the N-Boc deprotection of structu...
A cheap, less problematic, efficient and selective reagent for the removal of the t-butyl and 1-adam...
ZnBr2 in dichloromethane is a convenient reagent for mild and selective removal of the tert-butoxyca...
The extension of the deprotection procedure using HNO3 in CH2Cl2 to a number of appropriately select...
We report a mild method for the selective deprotection of the N-Boc group from a structurally divers...
The extension of the deprotection procedure of t-butylated carboxyl function using HNO3 in CH2Cl2 to...
A simple and mild procedure for the efficient deprotection of cyclic acetals and ketals, using ceriu...
We report an improved method for the selective deprotection of the <i>N</i>-phenylcarbamoyl group, w...
Copyright © 2012 Zinelaabine Cheraiet et al. This is an open access article distributed under the Cr...
<div><p></p><p>The efficient deprotection of several acetals, dithioacetals, and tetrahydropyranyl (...
A competent and fast method for the deprotection of trimethyl silyl group was attained by using chea...
A competent and fast method for the deprotection of trimethyl silyl group was attained by using chea...
An efficient, environmentally benign, highly facile and convenient synthetic protocol for the select...
A series of competition experiments has revealed that selective cleavage of N-benzyl-protected secon...
It is shown that prop-2-ynyl esters are useful protecting groups for carboxylic acids and that they ...
A simple, efficient, and alternative method has been developed for the N-Boc deprotection of structu...
A cheap, less problematic, efficient and selective reagent for the removal of the t-butyl and 1-adam...
ZnBr2 in dichloromethane is a convenient reagent for mild and selective removal of the tert-butoxyca...
The extension of the deprotection procedure using HNO3 in CH2Cl2 to a number of appropriately select...
We report a mild method for the selective deprotection of the N-Boc group from a structurally divers...
The extension of the deprotection procedure of t-butylated carboxyl function using HNO3 in CH2Cl2 to...
A simple and mild procedure for the efficient deprotection of cyclic acetals and ketals, using ceriu...
We report an improved method for the selective deprotection of the <i>N</i>-phenylcarbamoyl group, w...
Copyright © 2012 Zinelaabine Cheraiet et al. This is an open access article distributed under the Cr...
<div><p></p><p>The efficient deprotection of several acetals, dithioacetals, and tetrahydropyranyl (...
A competent and fast method for the deprotection of trimethyl silyl group was attained by using chea...
A competent and fast method for the deprotection of trimethyl silyl group was attained by using chea...
An efficient, environmentally benign, highly facile and convenient synthetic protocol for the select...
A series of competition experiments has revealed that selective cleavage of N-benzyl-protected secon...
It is shown that prop-2-ynyl esters are useful protecting groups for carboxylic acids and that they ...