A concise synthesis of 6H-Indolo[2,3-b]quinolines: Formal synthesis of Neocryptolepine

Kadam, H.K.; Parvatkar, P.T.; Tilve, S.G.

dc.contributor.author	Kadam, H.K.
dc.contributor.author	Parvatkar, P.T.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-04T03:20:09Z
dc.date.available	2015-06-04T03:20:09Z
dc.date.issued	2012
dc.identifier.citation	Synthesis-Stuttgart. 44(9); 2012; 1339-1342.	en_US
dc.identifier.uri	http://dx.doi.org/10.1055/s-0031-1290812
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2713
dc.description.abstract	A new two-step approach for the synthesis of 6H-indolo[2,3-b]quinolines is described using indole C3 alkylation and a one-pot reduction-cyclization-aromatization sequence. The synthesis of the parent 6H-indolo[2,3-b] quinoline system constitutes a formal synthesis of the alkaloid neocryptolepine (cryptotackieine).	en_US
dc.publisher	Thieme Publishing	en_US
dc.subject	Chemistry	en_US
dc.title	A concise synthesis of 6H-Indolo[2,3-b]quinolines: Formal synthesis of Neocryptolepine	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y