4940-52-7Relevant articles and documents
A Palladium-Catalyzed Oxa-(4+4)-Cycloaddition Strategy towards Oxazocine Scaffolds
Scuiller, Ana?s,Liu, Xueyang,Cordier, Marie,Garrec, Julian,Archambeau, Alexis
, p. 981 - 986 (2021/06/02)
A Pd-catalyzed oxa-(4+4)-cycloaddition between 1-azadienes and (2-hydroxymethyl)allyl carbonates is described. Aurone-derived azadienes furnished polycyclic 1,5-oxazocines in good yields. Interestingly, linear azadienes have also been involved and yielded monocyclic heterocycles with complete regioselectivity. DFT calculations were carried out to gain insight on this observation.
The Wittig reaction of benzofuran-2,3-diones
Takeuchi,Chosi,Tomozane,Yoshida,Yamato
, p. 2265 - 2267 (2007/10/02)
-
Synthesis of Pyridobenzofurans
Sarbagya, D. P.,Rangachari, K.,Mazumdar, A. K. D.,Banerji, K. D.
, p. 891 - 893 (2007/10/02)
Some diarylpyridobenzofurans have been conveniently synthesised in 50-65percent yield by the condensation of 2-arylidene-6-methoxycoumaran-3-ones (III) with phenacylpyridinium halides in the presence of ammonium acetate.In a similar manner some 5-h