1615-22-1Relevant articles and documents
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
Efficient oxidative conversion of aldehydes to 2-substituted oxazolines and oxazines using (diacetoxyiodo)benzene
Karade, Nandkishor N.,Tiwari, Girdharilal B.,Gampawar, Sumit V.
, p. 1921 - 1924 (2008/03/27)
An efficient synthesis of 2-substituted oxazolines from aldehydes and 2-amino alcohol using (diacetoxyiodo)benzene as an oxidant, is reported. (Diacetoxyiodo)benzene acts as a mild dehydrogenating agent to convert the initially formed oxazolidine from ald
Reactions of 2-(Tributylstannyl)-4,4-dimethyl-2-oxazoline with Organic Halides. Unusual Product from Aroyl Halide
Kosugi, Masanori,Fukiage, Akio,Takayanagi, Mitsuhiro,Sano, Hiroshi,Migita, Toshihiko,Satoh, Mitsuo
, p. 1351 - 1354 (2007/10/02)
2-(Tributylstannyl)-4,4-dimethyl-2-oxazoline (1) reacted with aroyl chloride smoothly without any palladium catalyst to give the unusual product, bis(N-aroyl-4,4-dimethyl-2-oxazolinylidene) in good yields.The reaction of 1 with other types of halide neede
