Synthesis of the 2,3-Disubstituted Maleic Anhydride Segment of Tautomycin
- 1 January 1993
- journal article
- letter
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 1993 (10) , 737-738
- https://doi.org/10.1055/s-1993-22589
Abstract
The 2,3-disubstituted maleic anhydride segment of tautomycin has been synthesized by oxidation of 3,4-disubstituted furan employing singlet oxygen.Keywords
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