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Gold(I)-Catalyzed Domino Reaction of Allyl 2-en-4-ynyl Ethers to 1,3,6-Trien-4-yl Ketones

机译:黄金(i) - 丙烷2-烯-4-烯基醚的催化剂反应1,3,6-三烯-4-烯酮酮

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摘要

The gold(I)-catalyzed reaction of allyl 2-en-4-ynyl ethers provides stereoselectively (Z)-1,3,6-trienes with an acyl substitutent in the 4-position. The reaction proceeds through an oxygen transfer along the chain and a clean allylic inversion. This complements the preceding work by Gagosz, who obtained furan derivatives in his investigation of similar substrates with terminal alkynyl groups.10,16 The only drawback of this mechanistically new pathway is the instability of the products under the reaction conditions, which sometimes prevents their isolation in high yields.
机译:烯丙基2-ZEN-4-炔基醚的黄金(I) - 催化反应,在4-位在4-位替代酰基取代,提供立体选择性(Z)-1,3,6------烯烯。 反应通过沿链条的氧气转移和清洁的烯丙基反转进行。 这补充了Gagosz的前一班,他在他对末端炔基类似底物的调查中获得了呋喃衍生物.10,16,这个机械主义新途径的唯一缺点是在反应条件下的产品的不稳定性,有时会阻止其分离 高产率。

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