Saritha Rajendhiran, Annes Sesuraj Babiola, Ramesh Subburethinam
Department of Chemistry, School of Chemical and Biotechnology, SASTRA Deemed University Thanjavur 613401 Tamil Nadu India
RSC Adv. 2021 Apr 15;11(23):14079-14084. doi: 10.1039/d1ra02372a. eCollection 2021 Apr 13.
Highly regioselective organo photocatalysis of 4CzIPN (1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene) for the arylation of 2-indazole is demonstrated. The present synthetic route provides a highly safe and easily accessible aniline precursor as an arylation reagent. The photoactivated 4CzIPN organocatalyst is found to be more efficient for single electron transfer without any organic base for the radical reaction. The carbazole-based photocatalyst (4CzIPN) with wide redox potential is stable and recyclable for further reaction transformations. Many indazole and aniline derivatives were used in the reaction and provided the arylated indazole derivatives in good to excellent yield.
已证明4CzIPN(1,2,3,5-四(咔唑-9-基)-4,6-二氰基苯)对2-吲唑进行芳基化反应具有高度区域选择性的有机光催化作用。目前的合成路线提供了一种高度安全且易于获得的苯胺前体作为芳基化试剂。发现光活化的4CzIPN有机催化剂在无任何用于自由基反应的有机碱的情况下,单电子转移效率更高。具有宽氧化还原电位的咔唑基光催化剂(4CzIPN)稳定且可循环用于进一步的反应转化。许多吲唑和苯胺衍生物用于该反应,并以良好至优异的产率提供芳基化的吲唑衍生物。