34099-33-7Relevant academic research and scientific papers
Highly effective opening of epoxides with aromatic amines in presence of β-Cyclodextrin in water
Tang, Siping,Xu, Zhifeng,Li, Junhua,Deng, Peihong,Feng, Lanyong
, p. 1165 - 1170 (2018)
This paper reports a simple, mild, and convenient method to synthesize β-amino alcohols. These β-amino alcohols were achieved in excellent yields (80-96 %) by ring-opening reaction of oxiranes with aromatic amines catalyzed by β-cyclodextrin at 30 oC in w
Fe(III) substituted Wells-Dawson type polyoxometalate: An efficient catalyst for ring opening of epoxides with aromatic amines
Aramesh,Yadollahi,Mirkhani
, p. 37 - 40 (2013/02/26)
Various β-aminoalcohols were prepared by the ring opening reaction of epoxides with aromatic amines in the presence of Fe(III) substituted Wells-Dawson type polyoxometalate, α2-[(n-C4H 9)4N]7P2/
Potassium dodecatungstocobaltate trihydrate (K5CoW 12O40·3H2O) as an efficient catalyst for aminolysis of epoxides
Rafiee,Tangestaninejad, Shahram,Habibi,Mirkhani
, p. 3673 - 3681 (2007/10/03)
Aminolysis of epoxides using various amines was catalyzed with potassium dodecatungstocobaltate trihydrate in a convenient and efficient method with good selectivities.
