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N-Alkoxyimidoyl Bromides as a New and Efficient Coupling Partner in Pd-Catalyzed Stille Reaction
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N-Alkoxyimidoyl Bromides as a New and Efficient Coupling Partner in Pd-Catalyzed Stille Reaction
N-Alkoxyimidoyl Bromides as a New and Efficient Coupling Partner in Pd-Catalyzed Stille Reaction
Sukbok Chang
Sukbok Chang
ML
Myunghee Lee
Myunghee Lee
SK
Sunggak Kim
Sunggak Kim
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27 September 2001
journal article
letter
Published by
Georg Thieme Verlag KG
in
Synlett
Vol. 2001
(10)
,
1557-1558
https://doi.org/10.1055/s-2001-17480
Abstract
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.
Keywords
CATALYSIS
CROSS-COUPLING
PALLADIUM
STILLE REACTION
TIN
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