Consequences of acid catalysis in concurrent ring opening and halogenation of spiroketals.

Consequences of acid catalysis in concurrent ring opening and halogenation of spiroketals.
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酸催化同时发生螺酮缩环开环和卤化的后果。

DOI:
10.1021/ol991078r
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发表时间:
1999
期刊:
影响因子:
5.2
通讯作者:
Fuchs,PL
Fuchs,PL
中科院分区:
化学1区
文献类型:
--
作者:
LaCour,TG;Tong,Z;Fuchs,PL

文献摘要

被引文献

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刘易斯酸和/或布朗斯台德酸添加剂允许螺缩酮在显著降低的温度下开环和卤化,以提高的产率和纯度生产ω-碘代烯醇醚,其可以在远端亲电中心的存在下进行进一步反应,得到新的类固醇骨架。
Lewis and/or Bronsted acid additives permit ring opening and halogenation of spiroketals at substantially reduced temperatures to produce ω-iodo enol ethers in improved yield and purity, which can undergo further reaction in the presence of distal electrophilic centers to give new steroid skeletons.