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Regio- and stereoselective reductive opening of diene-ester derived monoepoxides with palladium catalyst and dimethylamine–borane complex

✍ Scribed by Hervé David; Laurent Dupuis; Marie-George Guillerez; François Guibé


Book ID
104210207
Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
140 KB
Volume
41
Category
Article
ISSN
0040-4039

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✦ Synopsis


Monoepoxides of diene-esters are regio-and stereoselectively reduced to homoallylic alcohols by dimethylamine-borane complex in the presence of acetic acid and catalytic amounts of Pd(PPh 3 ) 4 .


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