Radical cyanocarbonylation using alkyl allyl sulfone precursors

Acyl cyanides have been prepared by the three-component coupling reactions comprised of alkyl allyl sulfones, carbon monoxide, and p-tolylsulfonyl cyanide under tin-free radical reaction conditions.
Publisher
Georg Thieme Verlag Kg
Issue Date
2005-12
Language
ENG
Keywords

AROMATIC ACYL CYANIDES; CARBON-MONOXIDE; AROYL CYANIDES; RATE CONSTANTS; OXIME ETHERS; IODIDES; CARBONYLATION; ALDEHYDES; KETONES; 1,2-DIKETONES

Citation

SYNLETT, v.20, no.20, pp.3160 - 3162

ISSN
0936-5214
DOI
10.1055/s-2005-921932
URI
http://hdl.handle.net/10203/87546
Appears in Collection
CH-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
  • Hit : 130
  • Download : 0
  • Cited 0 times in thomson ci
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡClick to seewebofscience_button
⊙ Cited 17 items in WoSClick to see citing articles inrecords_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0