134542-02-2Relevant articles and documents
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Rosen,Weber
, p. 47,48,50 (1977)
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Photoinduced Palladium-Catalyzed Carbofunctionalization of Conjugated Dienes Proceeding via Radical-Polar Crossover Scenario: 1,2-Aminoalkylation and beyond
Gevorgyan, Vladimir,Kurandina, Daria,Shing Cheung, Kelvin Pak,Yata, Tetsuji
supporting information, p. 9932 - 9937 (2020/06/27)
A photoinduced palladium-catalyzed 1,2-carbofunctionalization of conjugated dienes has been developed. This mild modular approach, which does not require employment of exogeneous photosensitizers and external oxidants, allows for efficient and highly regio- and stereoselective synthesis of a broad range of allylic amines from readily available 1,3-dienes, alkyl iodides, and amines. Employment of O- and C-nucleophiles toward oxyalkylation and dialkylation products was also demonstrated. A putative π-allyl palladium radical-polar crossover path is proposed as a key event in this three-component coupling process. The utility of this protocol is highlighted by its application for derivatization of several amine-containing drugs.
Mild and stereoconvergent palladium-catalyzed carbonyl alkenation reaction of α,β-unsaturated aldehydes
Braun, Manfred,Mross, Stefan,Schwarz, Ido
, p. 83 - 88 (2007/10/03)
The addition of preformed ketone and ester enolates to α,β-unsaturated aldehydes 1 followed by in situ protection leads to the carbonates 3, 7, 8, 11, and 13. They are converted into sensitive functionalized dienes 4, 9, 12, and 14 by a smooth palladium-c
