36243-96-6Relevant academic research and scientific papers
Water promoted iodotrimethyl silane reactions: Reductive cleavage of isoxazolidines and 2,1-benzisoxazoles to γ-amino alcohols and o-aminobenzophenones
Boruah, Monalisa,Konwar, Dilip
, p. 601 - 603 (2007/10/03)
Water promoted iodotrimethyl silane [ITMS] reductively cleaved isoxazolidines and 2,1-benzisoxazoles to γ-amino alcohols and o-aminobenzophenones respectively at shorter times and in higher yields at room temperature.
A convenient method for the production of ortho-amino and N-alkylaminobenzophenones
Dutta, Dilip Kumar,Konwar, Dilip
, p. 690 - 691 (2007/10/02)
ortho-Amino and N-alkylaminobenzophenones 3 have been prepared in good yields by the reductive cleavage of 2,1-benzisoxazole and its salts with Zn-AlCl3*6H2O/THF system.
A CONVENIENT SYNTHESIS OF 2-AMINOBENZOPHENONES USING IODOTRIMETHYLSILANE.
Konwar, D.,Boruah, R. C.,Sandhu, J. S.,Baruah, J. N.
, p. 1053 - 1058 (2007/10/02)
Iodotrimethylsilane reduces 3-aryl-2,1-benzisoxazole to o-amino-benzophenones.
