Аннотация:
Reactions of 3-amino-4H-chromeno[3,4-d]isoxazol-4-ones with acetic and trifluoroacetic anhydrides gave the corresponding acetyl derivatives, which were rearranged into 2-amino-4H-chromeno[3,4-d][1,3]oxazol-4-ones by heating in DMSO solution.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
V. Ya. Sosnovskikh, V. S. Moshkin, M. I. Kodess, “Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides”, Mendeleev Commun., 20:4 (2010), 209–211
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3041
https://www.mathnet.ru/rus/mendc/v20/i4/p209
Эта публикация цитируется в следующих 9 статьяx:
Al-Shimaa Badran, Aya Ahmed, Magdy A. Ibrahim, “Chemical Transformation of Chromones into Coumarins”, HETEROCYCLES, 102:12 (2021), 2277
Geetika Patel, Subhash Banerjee, “Review on Synthesis of Bio-active Coumarin-fused Heterocyclic Molecules”, COC, 24:22 (2020), 2566
Fernanda G. Medina, Joaquín G. Marrero, Mariana Macías-Alonso, Magdalena C. González, Iván Córdova-Guerrero, Ariana G. Teissier García, Soraya Osegueda-Robles, “Coumarin heterocyclic derivatives: chemical synthesis and biological activity”, Nat. Prod. Rep., 32:10 (2015), 1472
А. В. Галенко, А. Ф. Хлебников, М. С. Новиков, В. В. Пакальнис, Н. В. Ростовский, “Последние достижения химии изоксазола”, Усп. хим., 84:4 (2015), 335–377; A. V. Galenko, A. F. Khlebnikov, M. S. Novikov, V. V. Pakalnis, N. V. Rostovskii, “Recent advances in isoxazole chemistry”, Russian Chem. Reviews, 84:4 (2015), 335–377
Nayim Sepay, Sankar P. Dey, “Synthesis and Chemical Reactivity of 4‐Oxo‐4H‐1‐benzopyran‐3‐carboxaldehyde”, Journal of Heterocyclic Chem, 51:S1 (2014)
A. Brandi, M. Gensini, Organic Reaction Mechanisms Series, Organic Reaction Mechanisms · 2010, 2012, 419
V. Y. Sosnovskikh, V. S. Moshkin, “Novel data for the reaction of 3-cyano-(thio)chromones with N-nucleophiles”, Chem Heterocycl Comp, 48:1 (2012), 139
V. Ya. Sosnovskikh, V. S. Moshkin, M. Yu. Kornev, M. I. Kodess, “Reactions of 3-aminoisoxazolo[4,5-c]coumarin with benzoyl chloride: the first example of a preparative 1,2,4-oxadiazole–oxazole rearrangement”, Mendeleev Commun., 21:2 (2011), 110–111
Vyacheslav Ya. Sosnovskikh, Vladimir S. Moshkin, Mikhail I. Kodess, “ChemInform Abstract: Rearrangement of 3‐Aminoisoxazolo[4,5‐c]coumarins into 2‐Amino‐oxazolo[4,5‐c]coumarins Mediated by Carboxylic Acid Anhydrides.”, ChemInform, 41:49 (2010)
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