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Cu‐TEMPO Catalyzed Dehydrogenative Friedlander Annulation/sp3 C–H Functionalization/Spiroannulation towards Spiro[indoline‐3,3'‐pyrrolizin]‐2'‐yl)‐4‐phenylquinoline‐3‐Carboxylates.

Authors :
Pavithra, Dalavai
Ethiraj, Kannat Radhakrishnan
Nawaz Khan, Fazlur‐Rahman
Source :
European Journal of Organic Chemistry. 12/7/2020, Vol. 2020 Issue 45, p7035-7050. 16p.
Publication Year :
2020

Abstract

A series of spiro[indoline‐3,3'‐pyrrolizin]‐2'‐yl)‐4‐phenylquinoline‐3‐carboxylate 6 from 2‐amino‐5‐chlorobenzhydrol 1, benzyl alcohols 3, and methyl or ethyl acetoacetate 2 is reported by the Cu(OAc)2, TEMPO catalyzed dehydrogenative Friedlander annulation/sp3–CH‐functionalization/regioselective 1,3‐ dipolar cyclo‐ addition. Likewise, chimanine A analogues 7 were obtained using a similar strategy in DES (Deep Eutectic Solvents) as a reaction medium in excellent yields. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1434193X
Volume :
2020
Issue :
45
Database :
Academic Search Index
Journal :
European Journal of Organic Chemistry
Publication Type :
Academic Journal
Accession number :
147461639
Full Text :
https://doi.org/10.1002/ejoc.202001109