Selenocarbonyl synthesis using Woollins Reagent
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[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.
Bhattacharyya , P & Woollins , J D 2001 , ' Selenocarbonyl synthesis using Woollins Reagent ' Tetrahedron Letters , vol 42 , no. 34 , pp. 5949-5951 . DOI: 10.1016/S0040-4039(01)01113-3
This is the author's version of an article published in Tetrahedron Letters, available from http://www.sciencedirect.com
This work was funded by EPSRC
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