797035-69-9Relevant academic research and scientific papers
Total synthesis of phorboxazole B
Li, De-Run,Zhang, Dong-Hui,Sun, Cai-Yun,Zhang, Ji-Wen,Yang, Li,Chen, Jian,Liu, Bo,Su, Ce,Zhou, Wei-Shan,Lin, Guo-Qiang
, p. 1185 - 1204 (2007/10/03)
An efficient and highly convergent total synthesis of the potent antitumor agent phorboxazole B has been achieved. The synthetic strategy of this synthesis features: 1) a highly efficient substrate-controlled hydrogenation to construct the functionalized
A catalytic enantioselective hetero Diels-Alder approach to the C20-C32 segment of the phorboxazoles
Lucas, Brian S.,Luther, Laura M.,Burke, Steven D.
, p. 3757 - 3760 (2007/10/03)
(Chemical Equation Presented) An efficient synthesis of the C20-C32 segment of the phorboxazoles has been achieved using an enantioselective hetero Diels-Alder reaction catalyzed by Jacobsen's Cr(III) amino indanol Schiff base catalyst.
Toward the total synthesis of phorboxazole B: An efficient synthesis of the C20-C46 segment
De, Run Li,Cai, Yun Sun,Su, Ce,Lin, Guo-Qiang,Zhou, Wei-Shan
, p. 4261 - 4264 (2007/10/03)
(Chemical Equation Presented) An efficient synthesis of the C20-C46 segment of phorboxazole B is described. The key steps involved Hg(OAc) 2/I2-induced cyclization to construct the cis-tetrahydropyran moiety, the coupling of the meta
