885107-69-7Relevant academic research and scientific papers
Total Synthesis of (+)-SCH 351448: Efficiency via Chemoselectivity and Redox-Economy Powered by Metal Catalysis
Wang, Gang,Krische, Michael J.
, p. 8088 - 8091 (2016/07/16)
The polyketide natural product (+)-SCH 351448, a macrodiolide ionophore bearing 14 stereogenic centers, is prepared in 14 steps (LLS). In eight prior syntheses, 22-32 steps were required. Multiple chemoselective and redox-economic functional group interco
Total synthesis of (+)-SCH 351448
Zhu, Kaicheng,Panek, James S.
, p. 4652 - 4655 (2011/11/06)
A convergent synthesis of (+)-SCH 351448 (1), a monosodium salt of a C 2-symmetric macrodiolide, is described. Our approach is based on a [4 + 2] annulation with a chiral allyl silane (anti-5c) to assemble the pyran subunits. Homodimerization w
Efficient asymmetric synthesis of (+)-SCH 351448
Bolshakov, Sergei,Leighton, James L.
, p. 3809 - 3812 (2007/10/03)
(Chemical Equation Presented) An efficient and stereocontrolled total synthesis of (+)-SCH 351448, a novel activator of low-density lipoprotein receptor promoter, has been achieved with a longest linear sequence of 21 steps. Key steps include applications
