Stereocontrolled Total Synthesis of (-)-Englerin A

被引:41
|
作者
Takahashi, Keisuke [1 ]
Komine, Keita [1 ]
Yokoi, Yuichi [1 ]
Ishihara, Jun [1 ]
Hatakeyama, Susumi [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Nagasaki 8528521, Japan
来源
JOURNAL OF ORGANIC CHEMISTRY | 2012年 / 77卷 / 17期
关键词
FORMAL SYNTHESIS; MAGNESIUM MONOPERPHTHALATE; EPOXYNITRILE CYCLIZATION; BIOLOGICAL EVALUATION; OXIDATION; STEREOCHEMISTRY; CYCLOADDITION; ENGLERIN; INDIUM;
D O I
10.1021/jo301145r
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The total synthesis of (-)-englerin A, a potent and selective inhibitor of renal cancer cell lines, is described. The key feature indudes the stereocontrolled construction of the cyclopentane structure by taking advantage of a base-promoted epoxynitrile cyclization.
引用
收藏
页码:7364 / 7370
页数:7
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