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Published in 2025 at "Natural product research"
DOI: 10.1080/14786419.2025.2575122
Abstract: A novel stereoselective approach for synthesising a 10-membered β-resocylic macrolide, relgro (1) was established, utilising known chiral bis-epoxide and commercially made available Orsellinic acid. Key steps included Yamaguchi macrolactonization, hydroboration and alkylation of 1,3-dithiane as…
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Keywords:
total synthesis;
synthesis relgro;
alternative novel;
relgro ... See more keywords