Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans via a two-step sequential Michael-Evans aldol cyclization strategy: total synthesis of (+)-magnolone

Ganesh Pandey,Srikanth Luckorse,Vedavati G Puranik,Asha Budakoti

doi:10.1016/j.tetlet.2010.03.111

Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans via a two-step sequential Michael-Evans aldol cyclization strategy: total synthesis of (+)-magnolone

Ganesh Pandey, Srikanth Luckorse + Show 2 more

https://doi.org/10.1016/j.tetlet.2010.03.111

Copy DOI

Journal: Tetrahedron Letters	Publication Date: Apr 4, 2010
Citations: 9

Affiliation: National Chemical Laboratory

#Two-step Strategy #Synthesis Of Natural Product + Show 8 more

Abstract
Full-Text PDF
Similar Papers

Abstract

Abstract Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans is described employing a two-step Michael-Evans aldol cyclization strategy. The approach is successfully applied for the total synthesis of furano lignan natural product (+)-magnolone.

Full Text