Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1403194 | Journal of Molecular Structure | 2013 | 7 Pages |
Abstract
A bicyclic goniofupyranone core was synthesized from argentilactone using epoxide as an intermediate. The absolute stereochemistry of all asymmetric centers of a compound possessing the 2,6-dioxabicyclo [3.2.1]-octan-3-one moiety were unambiguously determined directly from X-ray data for the first time. Additionally, the absolute stereochemistry of the major epoxide was reported.
► Synthesis of a bicyclic goniofupyranone core from argentilactone. ► Absolute stereochemistry determined from X-ray data. ► Absolute stereochemistry of the epoxide from argentilactone.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ricardo Justino Alves, Olga Soares do Rego Barros, Lucilia Kato, Felipe Terra Martins, Cecilia Maria Alves de Oliveira,