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Carbonylation of alkynols catalyzed by Pd(II)/2-PyPPh2 dissolved in organic solvents and in ionic liquids: a facile entry to α-methylene γ- and δ-lactones

✍ Scribed by Crestina S Consorti; Gunter Ebeling; Jaı̈rton Dupont


Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
94 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


The carbonylation of terminal 3-alkyn-1-ols and 1-alkyn-4-ols by Pd(OAc) 2 associated with 2-(diphenylphosphino)pyridine (2-PyPPh 2 ) dissolved in organic solvents or in 1-n-butyl-3-methyl imidazolium ionic liquids affords quantitatively and selectively exo-a-methylene gand d-lactones, respectively. In the case of the reactions performed in ionic liquids (biphasic conditions), the lactones were isolated by simple distillation and the ionic catalyst solution can be reused.


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