Solid state oxidation of 1,4-dihydropyridines to pyridines using phenyliodine(III) bis(trifluoroacetate) or elemental sulfur

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DC Field	Value	Language
dc.contributor.author	Kumar, Dalip	-
dc.date.accessioned	2021-10-27T04:23:48Z	-
dc.date.available	2021-10-27T04:23:48Z	-
dc.date.issued	1999	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlehtml/1999/p1/a809494b	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3098	-
dc.description.abstract	A solventless oxidation of 1,4-dihydropyridines is effected by phenyliodine(III) bis(trifluoroacetate) (PIFA) at room temperature or elemental sulfur under microwave irradiation conditions. Dealkylation at the 4-position in the cases of ethyl, isopropyl and benzyl substituted dihydropyridine derivatives with PIFA is circumvented by an alternative general procedure using elemental sulfur which provides pyridines in good yields.	en_US
dc.language.iso	en	en_US
dc.publisher	RSC	en_US
dc.subject	Chemistry	en_US
dc.subject	1,4-dihydropyridines	en_US
dc.subject	Phenyliodine(III)	en_US
dc.subject	Bis(trifluoroacetate)	en_US
dc.title	Solid state oxidation of 1,4-dihydropyridines to pyridines using phenyliodine(III) bis(trifluoroacetate) or elemental sulfur	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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