174175-57-6Relevant articles and documents
Expanding the versatility of Schwartz' reagent: Hydrozirconation of vinylic acid and acetylenic acyl silanes
Lipshutz,Lindsley,Bhandari
, p. 4669 - 4672 (1994)
By virtue of a triisopropylsilyl acyl silane contained with a substrate undergoing hydrozirconation, chemospecificity can be realized favoring addition across the alkene or alkyne, rather than competitive 1,2-addition of hydride to the carbonyl portion of
Stereoselective preparation of functionalized alkenylmagnesium reagents via an iodine-magnesium exchange reaction
Rottlaender, Mario,Boymond, Laure,Cahiez, Gerard,Knochel, Paul
, p. 1080 - 1081 (1999)
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Iridium-catalyzed regioselective decarboxylative allylation of β-ketoacids: Efficient construction of γ,δ-unsaturated ketones
Chen, Shu-Jie,Lu, Guo-Ping,Cai, Chun
supporting information, p. 11512 - 11514 (2016/01/15)
A highly regioselective protocol for the direct synthesis of γ,δ-unsaturated ketones from β-ketoacids and allylic alcohols was proposed and accomplished relying on the combination of [Ir(cod)Cl]2 and 10-camphorsulfonic acid via decarboxylative allylation.
t-Bu-Amphos-RhCl3·3H2O: A highly recyclable catalyst system for the cross-coupling of aldehydes and aryl- and alkenylboronic acids in aqueous solvents
Huang, Rongcai,Shaughnessy, Kevin H.
, p. 4484 - 4486 (2007/10/03)
The combination of t-Bu-Amphos and RhCl3·3H2O gave the first highly recyclable catalyst for the coupling of aryl- and vinylboronic acids with aldehydes in aqueous solvents. The Royal Society of Chemistry 2005.
