Chatare, Vijay K.; Andrade, Rodrigo B. published an article in 2017, the title of the article was Total Synthesis of (-)-Albocycline.Product Details of 3976-69-0 And the article contains the following content:
The macrolactone natural product (-)-albocycline (I) is a promising antibiotic candidate for the treatment of both methicillin resistant Staphylococcus aureus (MRSA) and vancomycin-resistant strains. Herein, we report a concise total synthesis of (-)-albocycline in 14 steps from com. available Me (R)-3-hydroxybutyrate. Novel key steps include the highly regio- and stereoselective reactions of chiral N-sulfinyl metallodienamines (NSMDs) with aldehydes and the Davis oxaziridine, in addition to the Horner-Wadsworth-Emmons olefination of N-sulfinyl imines. The experimental process involved the reaction of (R)-Methyl 3-hydroxybutanoate(cas: 3976-69-0).Product Details of 3976-69-0
The Article related to albocycline total synthesis regioselective stereoselective, n-sulfinyl metallodienamine, albocycline, antibiotics, total synthesis, Biomolecules and Their Synthetic Analogs: Other Bacterial and Fungal Metabolites and other aspects.Product Details of 3976-69-0
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics