摘要A strategy for the synthesis of spiroketal compounds through a tandem iodocyclization of 1-(2-ethynylphenyl)-4-hydroxybut-2-yn-1-one derivatives is presented. This reaction could …
A strategy for the synthesis of spiroketal compounds through a tandem iodocyclization of 1- (2-ethynylphenyl)-4-hydroxybut-2-yn-1-one derivatives is presented. This reaction could …
A strategy for the synthesis of spiroketal compounds through a tandem iodocyclization of 1- (2-ethynylphenyl)-4-hydroxybut-2-yn-1-one derivatives is presented. This reaction could …
[引用][C]Facile Synthesis of Halogenated Spiroketals via a Tandem Iodocyclization.