135283-68-0Relevant academic research and scientific papers
Convergent Synthesis of Kibdelone C
Dai, Yihua,Ma, Feixia,Shen, Yanfang,Xie, Tao,Gao, Shuanhu
, p. 2872 - 2875 (2018)
The synthesis of kibdelone C, a polycyclic natural xanthone isolated from a soil actinomycete, was achieved through a convergent approach. A 6?€-electrocyclization was applied to construct the highly substituted dihydrophenanthrenol fragment (B-C-D ring). InBr3-promoted lactonization was employed to build the isocoumarin ring, which served as a common precursor for the formation of isoquinolinone ring (A-B ring). A key DMAP-mediated oxa-Michael/aldol cascade reaction was developed to install the tetrahydroxanthone fragment (E-F ring). This approach provides a new solution to prepare its derivatives and structurally related natural products.
Total Synthesis of All Four Diastereomers of 2-Acetamido-2,4-dideoxy-D-hexapyranose as Potential Competitive Inhibitors of N-Acetylneuraminic Acid Synthase
Mulzer, Johann,Seilz, Carsten,Luger, Peter,Weber, Manuela,Reutter, Werner
, p. 947 - 955 (2007/10/02)
A nine-step gram-scale total synthesis of all four diastereomers 3-6 of 2-acetamido-2,4-dideoxy-D-hexapyranose from aldehyde 9, a known derivative of (S)-malic acid, is described. Key Words: Deoxymannosamine / Carbohydrates, total synthesis of / Glycoprot
