Total Synthesis of Plakortone B

被引:18
作者
Xie, Xin-Gang [1 ,2 ]
Wu, Xun-Wei [1 ,2 ]
Lee, Hing-Ken [1 ,2 ]
Peng, Xiao-Shui [1 ,2 ]
Wong, Henry N. C. [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Dept Chem, Ctr Novel Funct Mol, Inst Chinese Med, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Inst Mol Technol Drug Discovery & Synth, Shatin, Hong Kong, Peoples R China
关键词
asymmetric synthesis; chirality; natural products; plakortone B; structure elucidation; ABSOLUTE STEREOCHEMISTRY; SECONDARY ALCOHOLS; DERIVATIVES; EXPRESSION; MECHANISM; OXIDATION; ALDEHYDES; KETONES; ALKYNES; SERIES;
D O I
10.1002/chem.201000189
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Plakortone B is a naturally occurring bicyclic[3.3.0]furanolactone compound with attractive bioactivities. Although the relative configuration of plakortone B's central core had been established by NMR spectroscopic methods, the absolute configuration of its four stereocenters remained unknown. In the present paper, all four possible isomers of plakortone B were synthesized and one of these molecules was round to be identical with the natural plakortone B on the basis of H-1. C-13 NMR spectra and specific rotation comparisons. Thus, the absolute configuration of the natural plakortone B was determined to be (3S.4S,6R.10R).
引用
收藏
页码:6933 / 6941
页数:9
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