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Synlett 1993; 1993(10): 737-738
DOI: 10.1055/s-1993-22589
DOI: 10.1055/s-1993-22589
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Synthesis of the 2,3-Disubstituted Maleic Anhydride Segment of Tautomycin
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Publikationsverlauf
Publikationsdatum:
19. März 2002 (online)
The 2,3-disubstituted maleic anhydride segment of tautomycin has been synthesized by oxidation of 3,4-disubstituted furan employing singlet oxygen.