Synthesis of homoallylic alcohols via palladium-catalyzed coupling of organomercurials and vinylic oxetanes

1988 ◽  
Vol 29 (40) ◽  
pp. 5069-5072 ◽  
Author(s):  
Richard C. Larock ◽  
Sandra K. Stolz-Dunn
ChemCatChem ◽  
2014 ◽  
Vol 6 (2) ◽  
pp. 561-566 ◽  
Author(s):  
Liangbin Huang ◽  
Qian Wang ◽  
Wanqing Wu ◽  
Huanfeng Jiang

Synlett ◽  
2020 ◽  
Vol 31 (13) ◽  
pp. 1323-1327
Author(s):  
Yoshikazu Horino ◽  
Juri Sakamoto ◽  
Miki Murakami ◽  
Miki Sugata

A synthesis of (Z)-alkene-containing linear conjugated dienyl homoallylic alcohols by using a palladium-catalyzed three-component reaction has been developed. This method shows good functional-group compatibility and generality, with high diastereoselectivity. Additionally, in many cases, the present method controls the alkene stereochemistry of the newly formed C–C bond and overcomes the inherent preference for (E)-alkene formation, giving (Z,E)- and (Z,Z)-products.


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