| Literature DB >> 33267583 |
Arun K Ghosh1, Shivaji B Markad1, William L Robinson1.
Abstract
We describe an enantioselective synthesis of (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-ol which is a key subunit of darunavir, a widely used HIV-1 protease inhibitor drug for the treatment of HIV/AIDS patients. The synthesis was achieved in optically pure form utilizing commercially available sugar derivatives as the starting material. The key steps involve a highly stereoselective substrate-controlled hydrogenation, a Lewis acid catalyzed anomeric reduction of a 1,2-O-isopropylidene-protected glycofuranoside, and a Baeyer-Villiger oxidation of a tetrahydrofuranyl-2-aldehyde derivative. This optically active ligand alcohol was converted to darunavir efficiently.Entities:
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Year: 2020 PMID: 33267583 PMCID: PMC7894212 DOI: 10.1021/acs.joc.0c02396
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354