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Site-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Amination

Authors
Ban, JaeyoungLim, MinkyungShabbir, SairaBaek, JunghyunRhee, Hakjune
Issue Date
Mar-2020
Publisher
Georg Thieme Verlag
Keywords
N-acetylation; aryl homocoupling; Ullmann coupling reaction; Tauber carbazole synthesis; intramolecular amination
Citation
Synthesis, v.52, no.6, pp 917 - 927
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
Synthesis
Volume
52
Number
6
Start Page
917
End Page
927
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/1214
DOI
10.1055/s-0039-1690759
ISSN
0039-7881
1437-210X
Abstract
We synthesized various carbazoles from anilines through a three-step process with good overall yields (up to 48%). This process comprises N-acetylation, copper(0)-mediated Ullmann homocoupling, and acid-mediated intramolecular amination. It permits various functional-groups on the substrate. Scale-up of the developed three-step synthetic route to carbazoles was also demonstrated.
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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ERICA 공학대학 (ERICA 에너지바이오학과)
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