122950-95-2Relevant articles and documents
Enantioselective synthesis of (-)-γ-jasmolactone
Missio,Comasseto
, p. 4609 - 4615 (2007/10/03)
The title compound was prepared in seven steps starting from the commercially available 4-ketopimelic acid. The key step features an enantioselective lactonization promoted by PPL.
Enzyme-Catalyzed Enantioconvergent Lactonization of γ-Hydroxy Diesters in Organic Solvents
Gutman, Arie L.,Bravdo, Tamar
, p. 4263 - 4265 (2007/10/02)
A strategy has been developed for the enantioconvergent lactonization of symmetrical hydroxy diesters which exploits the prochiral stereospecificity of lipases in organic solvents.Using this approach, prochiral γ-hydroxypimelate diesters (2) were converte