کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1309202 | 975198 | 2010 | 6 صفحه PDF | دانلود رایگان |

In this paper, rapid and highly efficient tetrahydropyranylation of alcohols and phenols with 3,4-dihydro-2H-pyran (DHP) in the presence of catalytic amounts of high-valent tin (IV) tetraphenylporphyrinato trifluoromethanesufonate, [SnIV(TPP)(OTf)2] is reported. In this catalytic system, primary, secondary and tertiary alcohols as well as phenols were converted to their corresponding tetrahydropyranyl ethers (THP-ethers) in excellent yields and short reaction times at room temperature. It is noteworthy that this method can be used for chemoselective tetrahydropyranylation of primary alcohols in the presence of secondary and tertiary alcohols and phenols. The catalyst was reused several times in the protection reactions without loss of its catalytic activity.
Rapid and highly efficient tetrahydropyranylation of primary, secondary and tertiary alcohols as well as phenols with 3,4-dihydro-2H-pyran (DHP) in the presence of catalytic amounts of high-valent [SnIV(TPP)(OTf)2] is reported. The corresponding tetrahydropyranyl ethers (THP-ethers) were obtained in excellent yields and short reaction times at room temperature. The catalyst was reused several times without loss of its catalytic activityFigure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 363, Issue 7, 20 April 2010, Pages 1523–1528