112606-72-1Relevant articles and documents
Optically operated second order optical effects in some substituted 4-(5-nitro-1,3-benzoxazol-2-yl)aniline chromophores
Szlachcic,Fedorchuk,Danel,Jarosz,El Naggar,Albassam,Wojciechowski,Gondek,Uchacz,Stadnicka,Lakshminarayana,Kityk
, p. 333 - 341 (2017)
In this work, we report on second order nonlinear optical (NLO) susceptibilities of some substituted 4-(5-nitro-1,3-benzoxazol-2-yl)aniline chromophores that were embedded into photopolymer matrices. Depending on the photo-induced nitrogen laser (waveleng
Synthesis of Benzoxazoles Using Electrochemically Generated Hypervalent Iodine
Koleda, Olesja,Broese, Timo,Noetzel, Jan,Roemelt, Michael,Suna, Edgars,Francke, Robert
, p. 11669 - 11681 (2017/11/24)
The indirect ("ex-cell") electrochemical synthesis of benzoxazoles from imines using a redox mediator based on the iodine(I)/iodine(III) redox couple is reported. Tethering the redox-active iodophenyl subunit to a tetra-alkylammonium moiety allowed for anodic oxidation to be performed without supporting electrolyte. The mediator salt can be easily recovered and reused. Our "ex-cell" approach toward the electrosynthesis of benzoxazoles is compatible with a range of redox-sensitive functional groups. An unprecedented concerted reductive elimination mechanism for benzoxazole formation is proposed on the basis of control experiments and DFT calculations.
Parallel synthesis of benzoxazoles via microwave-assisted dielectric heating
Pottorf, Richard S.,Chadha, Naresh K.,Katkevics, Martins,Ozola, Vita,Suna, Edgars,Ghane, Hadi,Regberg, Tor,Player, Mark R.
, p. 175 - 178 (2007/10/03)
A facile route to benzoxazoles has been developed using microwave-assisted dielectric heating. The ease of synthesis and workup allowed the parallel synthesis of a 48-membered library of benzoxazoles quickly and efficiently.