N-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction

Cited 13 time in webofscience Cited 0 time in scopus
  • Hit : 467
  • Download : 0
N-Alkoxyimidoyl bromides have been successfully employed as an efficient organic partner in the Pd-catalyzed Stille coupling reaction with various organotin compounds, and the corresponding O-alkyloximes were obtained in good to excellent yields.
Publisher
GEORG THIEME VERLAG KG
Issue Date
2001-10
Language
English
Article Type
Article
Keywords

RADICAL ACYLATION APPROACH; OXIME ETHERS; ORGANOTIN COMPOUNDS; PALLADIUM; CHLORIDES

Citation

SYNLETT, no.10, pp.1557 - 1558

ISSN
0936-5214
URI
http://hdl.handle.net/10203/78292
Appears in Collection
CH-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 13 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0