A facile route to pyrroles, isoindoles and hetero fused analogues

Gabbutt, Christopher D., Hepworth, John D., Heron, B. Mark and Pugh, Samantha L. (2002) A facile route to pyrroles, isoindoles and hetero fused analogues. Journal of the Chemical Society, Perkin Transactions 1 (24). pp. 2799-2808. ISSN 1472-7781

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Abstract

Enamino acids derived from 1,2-dimethylaminomethylene- or 1,2-hydroxymethylene-carbonyl compounds and amino acids undergo a decarboxylative cyclisation to pyrroles, isoindoles and other fused pyrroles. A two atom ring expansion occurs preferentially with enamino acids from cyclohexane-1,3-diones and α-alkyl-α-amino acids leading to oxocino[2,3-c]pyrroles.

Information

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

URI:

https://eprints.hud.ac.uk/id/eprint/15044

Title:

A facile route to pyrroles, isoindoles and hetero fused analogues

Creators:

Gabbutt, Christopher D., Hepworth, John D., Heron, B. Mark and Pugh, Samantha L.

Identification Number:

10.1039/B209255G

Official URL:

http://dx.doi.org/10.1039/B209255G

Date:

November 2002

Subjects:

Q Science > Q Science (General)
Q Science > QD Chemistry

Schools:

School of Applied Sciences

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Item Type:

Article

Depositing User:

Sharon Beastall

Date Deposited:

25 Sep 2012 09:39

Revision:

13

Last Modified:

28 Aug 2021 11:21

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