6277-45-8Relevant articles and documents
Cyclization of Active Methylene Isocyanides with α-Oxodithioesters Induced by Base: An Expedient Synthesis of 4-Methylthio/Ethoxycarbonyl-5-acylthiazoles
Anil, Seegehalli M.,Kiran, Kuppalli R.,Rajeev, Narasimhamurthy,Rangappa, Kanchugarakoppal S.,Sadashiva, Maralinganadoddi P.,Swaroop, Toreshettahally R.
, p. 1444 - 1450 (2020/04/27)
Cyclization of tosylmethyl isocyanide with α-oxodithioesters in the presence of KOH is reported for the synthesis of 4-methylthio-5-acylthiazoles. Similarly, ethyl isocyanoacetate underwent cyclization with α-oxodithioesters to form 4-ethoxycarbonyl-5-acy
Acid-Catalyzed Condensation of o-Phenylenediammines and o-Aminophenols with α-Oxodithioesters: A Divergent and Regio? selective Synthesis of 2-Methylthio-3-Aryl/Heteroarylquinoxalines and 2-Acylbenzoxazoles
Anil, Seegehally M,Kiran, Kuppalli R,Rangappa, Kanchugarakoppal S,Sadashiva, Maralinganadoddi P,Shruthi, Jeegundipattana B,Sukrutha, Kodipura P,Swaroop, Toreshettahally R
, p. 4205 - 4214 (2019/11/14)
o-Phenylenediammines and o-Aminophenols were reacted with α-oxodithioesters in a highly regioselective fashion to give 2-methylthio-3-Aryl/heteroarylquinoxalines and 2-Acylbenzoxazoles in 55-94percent and 45-86percent, respectively, in the presence of p-T
Coupling of azomethine ylides with nitrilium derivatives of closo-decaborate clusters: A synthetic and theoretical study
Mindich, Aleksey L.,Bokach, Nadezhda A.,Kuznetsov, Maxim L.,Haukka, Matti,Zhdanov, Andrey P.,Zhizhin, Konstantin Yu.,Miltsov, Serguei A.,Kuznetsov, Nikolay T.,Kukushkin, Vadim Yu.
, p. 1075 - 1086 (2013/03/13)
The azomethine ylides p-R3C5H4N+CHCOC 6H4R2-p (3a: R3=H, R2=H, X=Br; 3b: R3=H, R2=Me, X=I; 3c: R3=H, R2=OMe, X=I; 3d: R3=H, R2=F, X=I; 3e: R3=Me, R2=Me, X=Br) react with the nitrile functio