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Selenocarbonyl synthesis using Woollins Reagent
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dc.contributor.author | Bhattacharyya, Pravat | |
dc.contributor.author | Woollins, John Derek | |
dc.date.accessioned | 2011-04-04T09:34:44Z | |
dc.date.available | 2011-04-04T09:34:44Z | |
dc.date.issued | 2001-08-20 | |
dc.identifier | 5673224 | |
dc.identifier | 0518146b-5258-4296-9084-c9f134644e3c | |
dc.identifier | 000170376800040 | |
dc.identifier | 0035920859 | |
dc.identifier.citation | Bhattacharyya , P & Woollins , J D 2001 , ' Selenocarbonyl synthesis using Woollins Reagent ' , Tetrahedron Letters , vol. 42 , no. 34 , pp. 5949-5951 . https://doi.org/10.1016/S0040-4039(01)01113-3 | en |
dc.identifier.issn | 0040-4039 | |
dc.identifier.other | ORCID: /0000-0002-1498-9652/work/31779295 | |
dc.identifier.uri | https://hdl.handle.net/10023/1776 | |
dc.description | This work was funded by EPSRC | en |
dc.description.abstract | [PhP(Se)(mu -Se)](2) selenates secondary and tertiary amides to the corresponding selenoamides in 30-70% yields at 130 degreesC in toluene and indolizine-3-aldehydes to selenoaldehydes in 40-59% yield at 25 degreesC. (C) 2001 Elsevier Science Ltd. All rights reserved. | |
dc.format.extent | 73121 | |
dc.language.iso | eng | |
dc.relation.ispartof | Tetrahedron Letters | en |
dc.subject | Selenoamide | en |
dc.subject | Selenoaldehyde | en |
dc.subject | Selenation | en |
dc.subject | Woollins reagent | en |
dc.subject | Telluroamides | en |
dc.subject | Selenoamides | en |
dc.subject | Selenide | en |
dc.subject | QD Chemistry | en |
dc.subject.lcc | QD | en |
dc.title | Selenocarbonyl synthesis using Woollins Reagent | en |
dc.type | Journal article | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.identifier.doi | 10.1016/S0040-4039(01)01113-3 | |
dc.description.status | Peer reviewed | en |
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