Total Synthesis of (-)-Gardmultimine A
pubmed.ncbi.nlm.nih.gov › 32096647The first total synthesis of Gardneria oxindole alkaloid (-)-gardmultimine A has been achieved in 19 steps from d-tryptophan in a fully stereocontrolled manner. This synthesis features (1) an Ir-catalyzed regioselective C-H borylation/oxidation sequence to introduce the C12 methoxyl group, (2) a stereocontrolled oxidative rearrangement of indole to construct the spirooxindole motif, and (3) an ...
Total Synthesis of (-)-DaphnezominesA and B
capricorn.bc.edu › lsy › total-synthesisDec 16, 2020 · Total Synthesis of (-)-DaphnezominesA and B Chao Li’s group J. Am. Chem. Soc. 2020, 142, 15240 belong to the Daphniphyllumalkaloids family isolated from plants Daphniphyllum biological activities including anticancer, anti-HIV and anti-oxidant DaphnezomineA-type: aza-adamantane core bearing a carbinolamine bridge system.