Conversion of alkynes to cyclic imides and anhydrides using reactive iron carbonyls prepared from Fe(CO) < inf > 5 < /inf >  and Fe < inf > 3 < /inf > (CO) < inf > 12 < /inf >

dc.contributor.author	Periasamy, Mariappan
dc.contributor.author	Rameshkumar, Chellappan
dc.contributor.author	Mukkanti, Amere
dc.date.accessioned	2022-03-27T09:09:32Z
dc.date.available	2022-03-27T09:09:32Z
dc.date.issued	2002-04-22
dc.description.abstract	Alkyne-iron carbonyl complexes, prepared using Fe(CO)5-NaBH4-CH3COOH-amine-alkyne and Fe3(CO)12-amine-alkyne reagent systems, react with excess of amine at 25 °C to give cyclic imides in moderate to good yields. Further, unsaturated iron carbonyl species, prepared using the Fe(CO)5-pyridine-N-oxide system, react with alkynes to give the corresponding anhydrides. © 2002 Published by Elsevier Science B.V.
dc.identifier.citation	Journal of Organometalic Chemistry. v.649(2)
dc.identifier.issn	0022328X
dc.identifier.uri	10.1016/S0022-328X(02)01129-4
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0022328X02011294
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12509
dc.subject	Alkynes
dc.subject	Cyclic imides
dc.subject	Double carbonylation
dc.subject	Iron carbonyl complexes
dc.title	Conversion of alkynes to cyclic imides and anhydrides using reactive iron carbonyls prepared from Fe(CO) < inf > 5 < /inf > and Fe < inf > 3 < /inf > (CO) < inf > 12 < /inf >
dc.type	Journal. Article
dspace.entity.type

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