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

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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)
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