
TY  - JOUR
A1  - Camp, D 
A1  - Jenkins, ID 
T1  - The Reaction of Thiols and &#945;,&#969;-Dithiols With Triphenylphosphine and Diisopropyl Azodicarboxylate
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1990
VL  - 43
IS  - 1
SP  - 161
EP  - 168
KW  - 
UR  - https://doi.org/10.1071/CH9900161 
N2  - &#945;,&#969;-Dithiols in the presence of triphenylphosphine and diisopropyl  azodicarboxylate are converted into a mixture of monomeric and polymeric disulfides. The product distribution is dependent on the alkyl chain length and the reaction conditions. In contrast to normal Mitsunobu reactions, disulfide bond formation is achieved with regeneration of triphenylphosphine. The mechanism of this reaction is discussed. 
ER  -

