TY - JOUR
T1 - Cascade Nucleophilic Addition-Cyclic Michael Addition of Arynes and Indoles Bearing Michael Acceptor
T2 - A Strategy to Construct Pyrroloacridines and Study of Their Physicochemical Properties
AU - Hazra, Gurupada
AU - Kundu, Sayantan
AU - Dandela, Rambabu
AU - Thirupathi, Barla
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/7/7
Y1 - 2023/7/7
N2 - A facile synthetic approach to 6H-pyrrolo[3,2,1-de]acridines has been developed by using cascade N-nucleophilic addition-cyclic Michael addition process of arynes and indoles substituted with Michael acceptors under metal-free conditions. Additionally, photophysical studies of a few of the newly synthesized pyrroloacridine compounds indicated good fluorescence emission properties.
AB - A facile synthetic approach to 6H-pyrrolo[3,2,1-de]acridines has been developed by using cascade N-nucleophilic addition-cyclic Michael addition process of arynes and indoles substituted with Michael acceptors under metal-free conditions. Additionally, photophysical studies of a few of the newly synthesized pyrroloacridine compounds indicated good fluorescence emission properties.
UR - http://www.scopus.com/inward/record.url?scp=85163439363&partnerID=8YFLogxK
U2 - 10.1021/acs.joc.3c00462
DO - 10.1021/acs.joc.3c00462
M3 - Article
AN - SCOPUS:85163439363
SN - 0022-3263
VL - 88
SP - 8493
EP - 8504
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 13
ER -