期刊
SYNLETT
卷 26, 期 1, 页码 6-30出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1379361
关键词
acylation; Diels-Alder reaction; electrophilic addition; halogenation; substituent effects
资金
- National Natural Science Foundation of China [21332008, 51373180]
- National Basic Research Program of China [2011CB932501]
Iptycenes are a class of aromatic compounds that contain several arene units fused to a bicyclo[2.2.2] octatriene bridgehead system. This unique, rigid, three-dimensional molecular structure provides several open electron-rich cavities with an abundance of reactive positions, and makes them useful for a wide range of applications. There is no doubt that the synthesis and reactions of iptycene derivatives with different functional groups form the fundamental basis of iptycene development. In this account, the synthesis of substituted iptycenes is described. In particular, the different synthetic strategies toward substituted triptycenes and pentiptycenes are the main focus.
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