Anthriporphyrinoids: Design, Synthesis, and Reactivity towards Diels-Alder Reaction

被引:3
|
作者
Yadav, Bharti [1 ]
Ravikanth, Mangalampalli [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Mumbai 400076, India
来源
JOURNAL OF ORGANIC CHEMISTRY | 2023年 / 88卷 / 13期
关键词
FRAMEWORK; CHEMISTRY; SUBUNIT;
D O I
10.1021/acs.joc.3c00953
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of non-aromatic anthripentaphyrinscontaining an anthraceneunit, two thiophenes, and two pyrrole rings as a part of a macrocyclicframework connected via three meso-carbons were synthesized.The crystal structure of one of the anthripentaphyrins revealed thatthe two thiophene rings were in an inverted orientation, and the macrocycleadopts a nonplanar Z-like ruffled structure. These anthriporphyrinoidsact as dienes and undergo Diels-Alder reaction with dienophilesto form stable non-aromatic Diels-Alder adducts.
引用
收藏
页码:9343 / 9351
页数:9
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