| Literature DB >> 31877050 |
Philemon Ngoje1,2, David Crich1,2,3,4.
Abstract
We describe the synthesis of the unusual bicyclic sugar bradyrhizose in 14 steps and a 6% overall yield from d-glucose. The synthesis involves the elaboration of a trans-fused carbocyclic ring onto the preexisting glucopyranose framework followed by adjustment of the oxidation levels. Key steps include radical extension of the glucopyranose side chain, ring closing metathesis, allylic oxidation, Luche reduction, hydroxy-directed epoxidation, and acid-catalyzed epoxide opening at the more substituted position.Entities:
Mesh:
Substances:
Year: 2019 PMID: 31877050 PMCID: PMC6980344 DOI: 10.1021/acs.orglett.9b04279
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005