An enantioselective desymmetrization approach to C9-substituted trans-hydrindene rings based on a diastereotopic group-selective intramolecular Diels-Alder reaction

被引：6

作者：

Azzi, Nadia

Griffen, Ed

Light, Mark

Linclau, Bruno

机构：

[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England

[2] AstraZeneca, Macclesfield SK10 4TG, Cheshire, England

[3] Xray Crystallog Ctr, Sch Chem, Southampton SO17 1BJ, Hants, England

来源：

CHEMICAL COMMUNICATIONS | 2006年 / 47期

关键词：

D O I：

10.1039/b607488j

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The synthesis of an achiral skipped bis(1,3-diene) substrate was achieved, which was shown to undergo an enantioselective, diastereotopic group-selective, intramolecular Diels-Alder reaction.

引用

页码：4909 / 4911

页数：3

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