Cyclic (Alkyl)amino Carbene Based Iron Catalyst for Regioselective Dimerization of Terminal Arylalkynes

dc.contributor.authorAdhikari, D.
dc.contributor.authorMandal, S.K.
dc.date.accessioned2020-12-01T06:34:37Z
dc.date.available2020-12-01T06:34:37Z
dc.date.issued2016
dc.descriptionOnly IISERM authors are available in the record.
dc.description.abstract[(cAAC)Fe(CO)4] (1) catalyzed head-to-head dimerization of terminal arylalkynes toward conjugated enynes in very high yield and high E selectivity (up to 84:16 E:Z). The protocol can be performed under extremely low catalyst loading down to 0.01 mol %, resulting in a high TON of 6500. A mechanistic pathway for arylalkyne dimerization has been proposed on the basis of a well-defined catalyst, an isolable intermediate, and quantum chemical calculations.en_US
dc.identifier.citationOrganometallics, 35(21), pp.3775–3780en_US
dc.identifier.otherhttps://doi.org/10.1021/acs.organomet.6b00703
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.organomet.6b00703
dc.identifier.urihttp://hdl.handle.net/123456789/2416
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCatalyzeden_US
dc.subjectHead-to-head dimerizationen_US
dc.subjectTerminalen_US
dc.subjectArylalkynesen_US
dc.titleCyclic (Alkyl)amino Carbene Based Iron Catalyst for Regioselective Dimerization of Terminal Arylalkynesen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Need to add pdf.odt
Size:
8.63 KB
Format:
OpenDocument Text
Description:

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: