Abstract:
A new route to poorly available 5-alkoxyindolizines has been developed by reaction of oxazolo[3,2-a]pyridinium salts with sodium alkoxides; the structures of three indolizines and one parent salt have been confirmed by X-ray diffraction analysis.
Document Type:
Article
Language: English
Citation:
E. V. Babaev, A. V. Efimov, A. A. Tsisevich, A. A. Nevskaya, V. B. Rybakov, “Synthesis of 5-alkoxyindolizines from oxazolo[3,2-a]pyridinium salts”, Mendeleev Commun., 17:2 (2007), 130–132
Linking options:
https://www.mathnet.ru/eng/mendc3402
https://www.mathnet.ru/eng/mendc/v17/i2/p130
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E. V. Babaev, “2-halogen-substituted pyridinium-N-phenacylides and their cycloiminium and acyclic analogs: 1. Synthesis of the parent salts, their betaine-ylides, and oxazolium analogs”, Ref. J. Chem., 1:2 (2011), 161
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E. V. Babaev, A. A. Nevskaya, I. V. Dlinnykh, V. B. Rybakov, “Heterocycles with a bridging nitrogen atom. 19. Development of routes for the synthesis of oxazoloisoquinolinium salts based on phenacylation of α-methyl-1(3)-isoquinolones”, Chem Heterocycl Comp, 45:1 (2009), 93
E. V. Babaev, V. L. Alifanov, A. V. Efimov, “Oxazolo[3,2-a]pyridinium and oxazolo[3,2-a]pyrimidinium salts in organic synthesis”, Russ Chem Bull, 57:4 (2008), 845
Eugene V. Babaev, Andrey V. Efimov, Alexander A. Tsisevich, Aleksandra A. Nevskaya, Victor B. Rybakov, “Synthesis of 5‐Alkoxyindolizines from Oxazolo[3,2‐a]pyridinium Salts.”, ChemInform, 38:37 (2007)