Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines.

Camp, Jason, Craig, Donald, Funai, Kiyohiko and White, Andrew J. P. (2011) Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines. Organic & Biomolecular Chemistry, 9 (22). pp. 7904-7912. ISSN 1477-0520

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Abstract

Microwave-assisted decarboxylative Claisen rearrangement (dCr) reactions of substituted acetate derivs. of 3-(hydroxyalkyl)indoles give de-aromatized products. The reactivity of the resultant compds. was evaluated. [on SciFinder(R)]

Item Type:	Article
Additional Information:	Unmapped bibliographic data: PY - 2011/// [EPrints field already has value set] M3 - 10.1039/c1ob06212c [Field not mapped to EPrints] JA - Org. Biomol. Chem. [Field not mapped to EPrints]
Uncontrolled Keywords:	decarboxylative Claisen rearrangement hydroxyalkyl indole acetate, crystal mol structure methyl tosyl tosylethylidene indoline
Subjects:	Q Science > Q Science (General) Q Science > QD Chemistry
Schools:	School of Applied Sciences
Related URLs:	Author
Depositing User:	Sara Taylor
Date Deposited:	13 Nov 2014 16:40
Last Modified:	28 Aug 2021 11:43
URI:	http://eprints.hud.ac.uk/id/eprint/22275

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