132161-94-5Relevant articles and documents
TBD-catalyzed ring opening of aziridines with silylated nucleophiles
Matsukawa, S.,Takahashi, H.,Harada, T.
, p. 406 - 414,9 (2013)
The ring opening of N-tosylaziridines with silylated nucleophiles catalyzed by 1,5,7-triazabicyclo[4,4,0]dec-5-ene (TBD) afforded the corresponding- functionalized sulfonamides in excellent yields under mild reaction conditions. Copyright
Lewis base catalyzed ring opening of aziridines with silylated nucleophiles
Minakata, Satoshi,Okada, Yuriko,Oderaotoshi, Yoji,Komatsu, Mitsuo
, p. 3509 - 3512 (2005)
(Chemical Equation Presented) The ring opening of N-tosylaziridines with trimethylsilylated nucleophiles, catalyzed by N,N,N′,N′- tetramethylethylenediamine, led to the production of β-functionalized sulfonamides in good to excellent yields with high regi
An efficient method for opening N -tosylaziridines with silylated nucleophiles by using polystyrene-supported 1,5,7-triazabicyclo[44.0]dec-5-ene as a reusable organocatalyst
Matsukawa, Satoru,Tsukamoto, Kumiko,Yasuda, Shiori,Harada, Takeru
supporting information, p. 2959 - 2965 (2013/11/06)
Polystyrene-supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene (PS-TBD) catalyzes the ring opening of N-tosylaziridines with trimethylsilyl cyanide, trimethylsilyl azide, or trimethylsilyl halides to give the corresponding products in high yields. PS-TBD can b
