A facile one-pot transformation of baylis-hillman adducts into unsymmetrical disubstituted maleimide and maleic anhydride frameworks: A facile synthesis of himanimide A

dc.contributor.author	Basavaiah, Deevi
dc.contributor.author	Devendar, Badugu
dc.contributor.author	Aravindu, Kunche
dc.contributor.author	Veerendhar, Ainelly
dc.date.accessioned	2022-03-27T09:01:36Z
dc.date.available	2022-03-27T09:01:36Z
dc.date.issued	2010-02-15
dc.description.abstract	Unsymmetrical, disubstituted maleimide and maleic anhydride frameworks have been accessed from Baylis-Hillman adducts in an operationally simple three-step (FriedelCrafts reaction, selective hydrolysis and cyclization), one-pot strategy. This strategy has been successfully extended to the synthesis of a representative bioactive compound, himanimide A (see scheme). (Chemical Equation Representation). © 2010 Wiley-VCH Verlag GmbH & Co. KGaA,.
dc.identifier.citation	Chemistry - A European Journal. v.16(7)
dc.identifier.issn	09476539
dc.identifier.uri	10.1002/chem.200902887
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/chem.200902887
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12289
dc.subject	Friedel-crafts reaction
dc.subject	Heterocycles himanimide a
dc.subject	Natural products
dc.subject	Synthetic methods
dc.title	A facile one-pot transformation of baylis-hillman adducts into unsymmetrical disubstituted maleimide and maleic anhydride frameworks: A facile synthesis of himanimide A
dc.type	Journal. Article
dspace.entity.type

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