1067-52-3Relevant articles and documents
Pereyre,Valade
, p. 489 (1969)
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Hill,J. et al.
, p. 314 - 315 (1963)
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A new method for the synthesis of stannyl ethers by acid-catalyzed reaction of alcohols with allyltributylstannane
Yamago, Shigeru,Yamada, Takeshi,Nishimura, Ryuji,Ito, Hiroki,Mino, Yosuke,Yoshida, Jun-Ichi
, p. 152 - 153 (2002)
Stannyl ethers are prepared by triflic acid-catalyzed reaction of alcohols with tributylstannane or allyltributylstannane at room temperature. The stannyl ethers thus prepared can be successfully used for the β-bromogycoside-mediated glycosylation reactions.
Effect of tributyltin alkoxides chain length on the ring-opening polymerization of ε-caprolactone: Kinetics studies by non-isothermal DSC
Limwanich, Wanich,Khunmanee, Sureerat,Kungwan, Nawee,Punyodom, Winita,Meepowpan, Puttinan
, p. 1 - 7 (2015)
The kinetics of ring-opening polymerization (ROP) of ε-caprolactone (ε-CL) initiated by 1.0 mol% of the tributyltin alkoxides (Bu3SnOR; R = Me, Et, nPr and nBu) was investigated by non-isothermal DSC technique. The DSC curves showed the depende
Brimage,Davidson
, p. 281 (1971)
Tin-Catalyzed Synthesis of 5-Substituted 1H-Tetrazoles from Nitriles: Homogeneous and Heterogeneous Procedures
Chrétien, Jean-Mathieu,Kerric, Gaelle,Zammattio, Fran?oise,Galland, Nicolas,Paris, Michael,Quintard, Jean-Paul,Le Grognec, Erwan
supporting information, p. 747 - 757 (2019/01/04)
The preparation of 5-substituted 1H-tetrazoles was efficiently achieved by reaction of trimethylsilylazide with nitriles using a triorganotin alkoxide precatalyst. The reaction mechanism was first investigated using a homogeneous tributyltin derivative and was explored through experimental investigations and DFT calculations. A heterogeneous version was then developed using a polymer-supported organotin alkoxide and afforded an efficient method for the preparation of tetrazoles in high yields with an easy work-up and a residual tin concentration in the desired products compatible for pharmaceutical applications (less than 10 ppm). (Figure presented.).