Optically active 1-substituted taurines, a type of important sulfur analogues of naturally occurring amino acids, and their N-benzyloxycarbonyl-protected derivatives were synthesized from the corresponding optically active beta-amino secondary alcohols in three steps via N-protection with benzyl chloroformate, substitution with thiolacetic acid under Mitsunobu conditions, and oxidation with performic acid. (c) 2005 Wiley Periodicals, Inc.Chemistry, MultidisciplinarySCI(E)EI14ARTICLE6466-4711
The first half of this dissertation describes the synthesis and biological activities of a series of...
An effective and versatile method was developed to synthesize N-benzyloxycarbonyl-protected and free...
Taurine and substituted taurines were synthesized efficiently from aziridines via ring-opening react...
N-Benzyloxycarbonyl protected alpha-substituted and alpha,beta-disubstituted taurines were synthesiz...
Various substituted taurines have been synthesized expeditiously and practically in satisfactory to ...
(±)trans 2-Aminocyclohexanesulfonic acid and (±)trans 2-aminocyclo-pentanesulfonic acid were prepare...
A series of 1,1 -disubstituted taurines was synthesized expeditiously from ketones via the Corey-Cha...
A series of 1-substituted taurines, including optically active taurines, were synthesized expeditiou...
A simple and efficient protocol for the synthesis of Nβ- Fmoc/Z-amino alkyl thiols is described. Th...
Sulfonic acids and its derivatives are an important class of organic compounds. There are many sulfo...
Taurine-containing water-soluble peptidomimetics were designed and synthesized. <i>N</i>-terminal ta...
Within the class of six- and seven-membered sulfur-containing cyclic ketimines and their derivatives...
A radical addition reaction and subsequent performic acid oxidation were used for the synthesis of 1...
Have been obtained 2-aminoethanesulfonic acid (taurine) from ethanolamine, sulfuric acid and sodium ...
Starting from N-protected aminoalkyl iodides and thiourea, an efficient synthesis of the correspondi...
The first half of this dissertation describes the synthesis and biological activities of a series of...
An effective and versatile method was developed to synthesize N-benzyloxycarbonyl-protected and free...
Taurine and substituted taurines were synthesized efficiently from aziridines via ring-opening react...
N-Benzyloxycarbonyl protected alpha-substituted and alpha,beta-disubstituted taurines were synthesiz...
Various substituted taurines have been synthesized expeditiously and practically in satisfactory to ...
(±)trans 2-Aminocyclohexanesulfonic acid and (±)trans 2-aminocyclo-pentanesulfonic acid were prepare...
A series of 1,1 -disubstituted taurines was synthesized expeditiously from ketones via the Corey-Cha...
A series of 1-substituted taurines, including optically active taurines, were synthesized expeditiou...
A simple and efficient protocol for the synthesis of Nβ- Fmoc/Z-amino alkyl thiols is described. Th...
Sulfonic acids and its derivatives are an important class of organic compounds. There are many sulfo...
Taurine-containing water-soluble peptidomimetics were designed and synthesized. <i>N</i>-terminal ta...
Within the class of six- and seven-membered sulfur-containing cyclic ketimines and their derivatives...
A radical addition reaction and subsequent performic acid oxidation were used for the synthesis of 1...
Have been obtained 2-aminoethanesulfonic acid (taurine) from ethanolamine, sulfuric acid and sodium ...
Starting from N-protected aminoalkyl iodides and thiourea, an efficient synthesis of the correspondi...
The first half of this dissertation describes the synthesis and biological activities of a series of...
An effective and versatile method was developed to synthesize N-benzyloxycarbonyl-protected and free...
Taurine and substituted taurines were synthesized efficiently from aziridines via ring-opening react...