A facile synthesis of 2H-indazoles under neat conditions and further transformation into aza-gcarboline alkaloid analogues in a tandem one-pot fashion†

Shinde, V and A, Sagar and N C, Chaitra and D S, Sharada (2014) A facile synthesis of 2H-indazoles under neat conditions and further transformation into aza-gcarboline alkaloid analogues in a tandem one-pot fashion†. RSC Advances, 4. pp. 34232-34236. ISSN 2046-2069

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Abstract

We have described a facile, microwave-assisted, catalyst-free and solvent-free approach to 2H-indazoles and further developed a robust tandem one-pot metal-free strategy for C–C bond formation at the C-3 position of 2H-indazoles leading to a unique class of aza-g-carboline alkaloid analogues. This straightforward expedient synthesis constitutes an interesting alternative to the existing conventional transition metal catalyzed reactions.

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IITH Creators:

IITH Creators	ORCiD
D S, Sharada	UNSPECIFIED

Item Type:

Article

Additional Information:

† Electronic supplementary information (ESI) available. CCDC 994876. For ESI and crystallographic data in CIF or other electronic format see DOI:10.1039/c4ra06838f

Subjects:

?? sub5.8 ??

Divisions:

Department of Chemistry

Depositing User:

Users 3 not found.

Date Deposited:

30 Sep 2014 06:41

Last Modified:

06 Jan 2016 11:23

URI:

http://raiithold.iith.ac.in/id/eprint/157