Intramolecular cyclization reactions of 5-halo- and 5-nitro-substituted furans
(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
Crawford, Kenneth R.,Bur, Scott K.,Straub, Christopher S.,Padwa, Albert
p. 3337 - 3340
(2007/10/03)
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