6H-Indolo[2,3-b]Quinoline: A recent synthetic comprehension

Kadam, H.K.; Tilve, S.G.

dc.contributor.author	Kadam, H.K.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2019-02-18T04:05:51Z
dc.date.available	2019-02-18T04:05:51Z
dc.date.issued	2019
dc.identifier.citation	Mini-Reviews in Organic Chemistry. 16(1); 2019; 35-42.	en_US
dc.identifier.uri	https://doi.org/10.2174/1570193X15666180528103548
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/5596
dc.description.abstract	The present review provides a comprehensive overview of the synthetic methods developed recently for 6H-Indolo[2,3-b]quinoline. The review is classified into the following: 1) inheriting indole skeleton and constructing quinoline ring; 2) inheriting quinoline skeleton and constructing indole ring, and 3) convergent strategies constructing both rings simultaneously or step by step. This review discusses the scope of multifunctional reactivity of indole and quinoline skeleton for constructing the desired indoloquinolines as explored in various research strategies.	en_US
dc.publisher	Bentham Science Publishers	en_US
dc.subject	Chemistry	en_US
dc.title	6H-Indolo[2,3-b]Quinoline: A recent synthetic comprehension	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y