117845-23-5Relevant articles and documents
Intramolecular cyclization reactions of 5-halo- and 5-nitro-substituted furans
Crawford, Kenneth R.,Bur, Scott K.,Straub, Christopher S.,Padwa, Albert
, p. 3337 - 3340 (2007/10/03)
(Matrix presented) Intramolecular cyclization reactions of 5-halo- and 5-nitro-substituted furanylamides were examined. The 2-alkoxy-5-bromofuran derivative 2 produced the rearranged dihydroquinone 6 (36%), a product from the rearrangement of the intermed
Chemistry of Furans: Part VI - Synthesis of 5-Amino-2-furanamides
Rai, Usha Kumari,Shanker, Birja,Singh, Sujan,Rao, R. Balaji
, p. 674 - 675 (2007/10/02)
5-Amino-2-furanamides (II) have been synthesised by the nucleophilic displacement of bromine in 5-bromo-2-furanamides by piperidine, pyrrolidine and morpholine.