18023-52-4Relevant articles and documents
Mild, Effective and Selective Method for the Silylation of Alcohols Using Silazanes Promoted by Catalytic Tetrabutylammonium Fluoride
Tanabe, Yoo,Murakami, Masanari,Kitaichi, Kazuto,Yoshida, Yoshihiro
, p. 8409 - 8412 (1994)
The presence of catalytic amounts (ca. 0.02 equiv.) of tetrabutylammonium fluoride (TBAF) significantly promoted the silylation of alcohols using a variety of available silazanes under mild conditions with high chemoselectivity, wherein the choice of sila
Room temperature silylation of alcohols catalyzed by metal organic frameworks
Dhakshinamoorthy, Amarajothi,Santiago-Portillo, Andrea,Concepción, Patricia,Herance, José R.,Navalón, Sergio,Alvaro, Mercedes,Garcia, Hermenegildo
, p. 2445 - 2449 (2017/07/24)
The commercial Al(OH)(BDC) (BDC: 1,4-benzenedicarboxylic acid) metal organic framework (Basolite A100) is a suitable heterogeneous catalyst for the silylation of benzylic and aliphatic alcohols by hexamethyldisilazane in toluene at room temperature. Al(OH
Highly efficient protection of alcohols and phenols catalysed by tin porphyrin supported on MIL-101
Zadehahmadi, Farnaz,Tangestaninejad, Shahram,Moghadam, Majid,Mirkhani, Valiollah,Mohammadpoor-Baltork, Iraj,Kardanpour, Reihaneh
, p. 209 - 215 (2015/03/30)
The catalytic activity of 5,10,15,20-tetrakis(4-aminophenyl)porphyrinatotin(IV) trifluoromethanesulfonate, [SnIV(TNH2PP)(OTf)2], supported on chloromethylated MIL-101, was investigated in the trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) and also their tetrahydropyranylation with 3,4-dihydro-2H-pyran. Excellent yields, mild reaction conditions, short reaction times and reusability of the catalyst without significant decrease in its initial activity are noteworthy advantages of this supported catalyst.