
TY  - JOUR
A1  - Baerlocher, Felix Jakob 
A1  - Baerlocher, Mark Otto 
A1  - Guckert, Kristal Dawn 
A1  - Langler, Richard Francis 
A1  - MacQuarrie, Stephanie Lee 
A1  - O'Connor, Paul Eric 
A1  - Sung, Gabriel Carl Yan 
T1  - Selected <font face="symbol">a</font>,<font face="symbol">a</font>'-Dimethyl Disulfides: Submicrogram Fungitoxins
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 2001
VL  - 54
IS  - 6
SP  - 397
EP  - 400
KW  - 
UR  - https://doi.org/10.1071/CH01046 
N2  - Recently developed synthetic methodology has been exploited for the preparation of an assortment of &#945;,&#945;&acute;-disubstituted disulfides including all three linkage isomeric types of &#945;,&#945;&acute;-diester dimethyl disulfides. Two of the diesters are very powerful antifungal agents against Aspergillus niger and Aspergillus flavus. An &#945;-ester &#945;&acute;-sulfone disulfide is the most powerful fungitoxin developed by this ongoing research effort. 
ER  -

