化学
烯丙基重排
特里斯
取代基
产量(工程)
立体化学
杯芳烃
组合化学
分子
有机化学
催化作用
生物化学
冶金
材料科学
作者
Martin Lepeintre,Julie Champciaux,Benoît Colasson,Ivan Jabin
标识
DOI:10.1021/acs.joc.3c02790
摘要
Few synthetic methodologies that yield tris-functionalized C3v-symmetrical calix[6]arenes have been reported. In this work, three allyl protecting groups are selectively placed in 1,3,5 alternate positions of three pristine calix[6]arenes, each differing by their substituent on the large rim, resulting in three new C3v-symmetrical molecular platforms. Removal of the protecting allylic groups gives access to sophisticated calix[6]arenes that can be further modified. The potential of these new C3v-symmetrical molecular platforms is notably exemplified through the development of a new family of calix[6]arene-based N ligands.
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