229643-15-6Relevant articles and documents
Synthesis of New P-substituted Iminophosphoranes Via Staudinger Raction and Antimicrobial Activity Evaluation
Madhava,Subramanyam,Thaslim Basha,Jawahar Babu,Naga Raju
, p. 16 - 21 (2016)
A class of two series of new P-substituted iminophosphoranes, N-(1,3-benzothiazol-2-ylmethyl)-N-(alkyl subtituted-λ5-phosphanylidene)amine 5(a-e) and N-(alkyl substituted-λ5-phosphanylidene)-(3,5-difluorophenyl)methanamine 9(a-e) was
Catalytic Aerobic Photo-oxidation of a Methyl Group on a Heterocycle to Produce an Aldehyde via Homolytic C-I Bond Cleavage caused by Irradiation with Visible Light
Nagasawa,Tachikawa,Yamaguchi,Tada,Miura,Itoh
supporting information, p. 178 - 182 (2016/02/14)
A new catalytic method was developed for photo-oxidizing the methyl group on aromatic heterocycles such as benzothiazole, benzoxazole, and quinoline to produce the corresponding aldehyde. This is the first report of the metal-free catalytic synthesis of benzothiazole-2-carboxaldehydes using molecular oxygen as the terminal oxidant.
Samarium Barbier reactions of α-iodomethyloxazoles and thiazoles with aliphatic aldehydes
Williams, David R.,Berliner, Martin A.,Stroup, Bryan W.,Nag, Partha P.,Clark, Michael P.
, p. 4099 - 4102 (2007/10/03)
(Chemical Equation Presented) The reductive coupling of substituted α-iodomethyloxazoles and thiazoles with aliphatic aldehydes under Barbier conditions provides an effective method for the direct incorporation of intact heterocyclic systems.