64073-85-4Relevant academic research and scientific papers
Use of Hypervalent Iodine in the Synthesis of Isomeric Dihydrooxazoles
Carlucci, Claudia,Tota, Arianna,Colella, Marco,Ronamazzi, Giuseppe,Clarkson, Guy J.,Luisi, Renzo,Degennaro, Leonardo
, p. 428 - 436 (2018/06/11)
[Figure not available: see fulltext.] A convenient synthesis of 2- and/or 3-oxazolines has been developed depending on the structure and stereochemistry of the starting amino alcohol. PhI(OAc)2 acted as oxidant on the intermediate imine, as sup
Synthesis, characterization and solid state structural studies of oxovanadium (IV) - O, N donor Schiff base chelates
Mishra,Pandey
, p. 94 - 97 (2007/10/03)
VO(IV)-complexes with the Schiff bases viz., 4-chlorobenzylidene-2-amino-4- chlorophenol (CAP), 4-dimethyl-aminobenzylidene-2-aminophenol (DAP) and 2-hydroxy-1-naphthylidene-4-bromoaniline (HBA) have been synthesized and characterized by elemental analyse
Hypervalent iodine(III) mediated synthesis of 2-substituted benzoxazoles
Prakash, Om,Batra, Anita,Sharma, Vijay,Saini, Rajesh K.,Verma, Rajender S.
, p. 1031 - 1034 (2007/10/03)
2-Substituted benzoxazoles (6a-j, 7a-e, 7j-l) have been synthesized via the oxidative intramolecular cyclization of Schiff's bases (4a-j, 5a-e, 5j-l) using iodobenzene diacetate (IBD) as an oxidant in dry methanol. A one-pot procedure for the synthesis of 6a-j, 7a-e and 7j-l starting from o-aminophenol/p-chloro-o- aminophenol and aldehydes has also been developed.
