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Construction of the Hexacyclic Core of Dispirocochlearoids A-C via a Diels-Alder Reaction 被引量:1
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作者 Qiang Fu Yonghui Wang Fajun Nan 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2022年第13期1566-1570,共5页
The natural products of dispirocochlearoids are complex Ganoderma meroterpenoids featuring a 6/6/5/6/6/6 ring system and are selective cox-2 inhibitors.Herein,we describe our progress regarding the total synthesis of ... The natural products of dispirocochlearoids are complex Ganoderma meroterpenoids featuring a 6/6/5/6/6/6 ring system and are selective cox-2 inhibitors.Herein,we describe our progress regarding the total synthesis of dispirocochlearoids A-C,in which a hexacyclic skeleton was constructed firstly.The key steps of this work involve an intermolecular[4+2]cycloaddition reaction,a ring cleavage approach via Ticla,and the installation of a profoundly sterically hindering lactone. 展开更多
关键词 Natural products dispirocochlearoids Hexacyclic skeleton CYCLOADDITION Total synthesis
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