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        Synthesis  2003(4): 0509-0512
DOI: 10.1055/s-2003-37650
   DOI: 10.1055/s-2003-37650
PAPER
© Georg Thieme Verlag Stuttgart · New YorkConversion of Alcohols to Thiols via Tosylate Intermediates
Further Information
            
               
                  
                        
                              Received
                              26 November 2002 
                      
Publication Date:
07 March 2003 (online)
            
         
      
   Publication History
Publication Date:
07 March 2003 (online)

Abstract
High yielding syntheses of mercapto terminated monodisperse dimer, trimer, and tetramer ethyleneoxide oligomers and of p-hydroxyphenethyl thiol via an alcohol-tosylate-thiol route are reported. Comparisons are made with the more conventional alcohol-bromide-thiol route.
Key Words
thiols - esters - alcohols - thiourea - ethyleneglycol oligomer
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            review, a similar synthesis involving conversion of a hydroxyl terminated poly(ethylene
            
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