@article { ISI:000236437400010,
	title = {Haval-Argade contrathermodynamic rearrangement of alkylidenesuccinimides to alkylmaleimides via the corresponding isoimides: a general approach to alkyl and dialkyl substituted maleimides},
	journal = {Tetrahedron},
	volume = {62},
	number = {15},
	year = {2006},
	month = {APR},
	pages = {3557-3563},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A simple and efficient access to alkyl and dialkyl substituted maleimides has been demonstrated via the new contrathermodynamic rearrangement of (E)-alkylidenesuccinimides to alkylinaleimides. The (E)-alkylidenesuccinimides obtained from the Wittig-condensation of N-arylmaleimide with aliphatic aldehydes oil regioselective hydrolysis furnished the corresponding (E)-alkylidenesuccinanilic acids in 95-98\% yields. The beta-alkylidenesuccinanilic acids oil treatment with cyanuric chloride in the presence of triethylamine gave the corresponding beta-alkylisomaleimides in 78-80\% yields via the beta-alkylideneisosuccinimides with the exocyclic to endocyclic carbon-carbon double bond migration. The kinetically controlled products alkylisomaleimides in refluxing acetic acid furnished the thermodynamically controlled alkylinaleimides in 98\% yield. The Wittig condensation of alkyl substituted isomaleimides/maleimides with aliphatic aldehydes gave the desired dialkyl substituted maleimides in high yields. A conversion of alpha-methylenesuccinanilic acids to alpha-methylisomaleimides has also been described, with 90\% yield. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	keywords = {alkyl and dialkylmaleimides, contrathermodynamic rearrangement, isomaleimides, maleimides, wittig coupling},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2006.01.091},
	author = {Haval, Kishan P. and N. P. Argade}
}
@article { ISI:000277129300005,
	title = {Facile synthesis of N-substituted maleimides},
	journal = {Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry},
	volume = {49},
	number = {4},
	year = {2010},
	month = {APR},
	pages = {487-488},
	publisher = {COUNCIL SCIENTIFIC \& INDUSTRIAL RES},
	address = {ANUSANDHAN BHAWAN, 2 RAFI MARG, NEW DELHI, 110001, INDIA},
	abstract = {<p>A simple and efficient method for the synthesis of N-substituted malemides from the corresponding maleamie acids under the phase transfer catalysis has been described</p>},
	keywords = {Maleamic acids, maleimides, phase transfer catalysis, synthesis},
	issn = {0376-4699},
	author = {Deshpande, Sunita R. and Maybhate, Shailaja P. and Likhite, Anjali P. and Chaudhary, Preeti M.}
}
