Formal total synthesis of triptolide
A new approach to the medicinally-important natural product triptolide is significantly shorter than previous syntheses, highly convergent and avoids the use of protecting groups; key features include two Diels-Alder reactions and a new deoxygenative aromatisation process.
|Collections||ANU Research Publications|
|01_Miller_Formal_total_synthesis_of_2008.pdf||664.69 kB||Adobe PDF||Request a copy|
Items in Open Research are protected by copyright, with all rights reserved, unless otherwise indicated.