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Total Synthesis of the Macrolide Antibiotic 5,6-Dihydrocineromycin B
Lutz F Tietze1, Ludwig Völkel1
1Institut für Organische Chemie der Universität Tammannstrasse 2, 37077 Göttingen (Germany) Fax: (+49) 551-39-9476.
Angewandte Chemie (International Ed. in English)
|May 2, 2018
Abstract:
Three building blocks are coupled convergently in the first total synthesis of the macrolide antibiotic 5,6-tetrahydrocineromycin B (1); the facial selective allylation of a methyl ketone is the key step of the synthesis. TBDMS=tert-butyldimethylsilyl, PMB=p-methoxybenzyl.
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