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Potassium dodecatangestocobaltate trihydrate (K5CoW12O40·3H2O): a mild and efficient catalyst for deprotection of dioxolanes and trimethylsilyl ethers

✍ Scribed by Mohammad H Habibi; Shahram Tangestaninejad; Iraj Mohammadpoor-Baltork; Valiollah Mirkhani; Bahram Yadollahi


Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
107 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis


Mild and easy deprotection of benzylic dioxolanes to carbonyl compounds (in refluxing dry acetone) and trimethylsilyl ethers to alcohols in acetonitrile at ambient temperature has been carried out in excellent yields under K 5 CoW 12 O 40 •3H 2 O (0.01 molar equiv.


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Potassium dodecatangestocobaltate trihyd
✍ Mohammad H Habibi; Shahram Tangestaninejad; Iraj Mohammadpoor-Baltork; Valiollah 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 59 KB

A simple, mild and effective method for tetrahydropyranylation of a variety of alcohols and cleavage of their tetrahydropyranyl ethers at ambient temperature in the presence of K 5 CoW 12 O 40 •3H 2 O as the catalyst with high turnovers is described.