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Trivalent organophosphorus reagent induced pinacol rearrangement of 4H-cyclopenta[2,1-b:3,4-b ']dithiophen-4-one

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In this Letter we report on the reaction of 4H-cyclopenta[2,1-b:3,4-b']dithiophen-4-one with various trivalent organophosphorus derivatives, with an emphasis on the final products depending on the applied reagents. No reaction occurred upon treatment with either triphenyl- or tricyclohexylphosphine, whereas addition of triethyl phosphite or tri(n-butyl)phosphine resulted in pinacol rearrangement. Structure elucidation of the isolated 5H-spiro(benzo[1,2-b:6,5-b']dithiophene-4,4'-cyclopenta[2,1-6:3,4-b']dithiophen)-5-one was achieved by combined NMR experiments, theoretical chemical shift and geometry calculations, and single crystal X-ray analysis. (C) 2012 Elsevier Ltd. All rights reserved.
Tijdschrift: TETRAHEDRON LETTERS
ISSN: 0040-4039
Issue: 6
Volume: 54
Pagina's: 526 - 529
Jaar van publicatie:2013
Trefwoorden:Chemistry, Organic, 4H-Cyclopenta[2,1-b:3,4-b ']dithiophene, Pinacol rearrangement, Trivalent organophosphorus reagents, Chemical shift calculations, X-ray diffraction
BOF-keylabel:ja
IOF-keylabel:ja
BOF-publication weight:1
CSS-citation score:1
Authors from:Government, Higher Education, Private
Toegankelijkheid:Closed