Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Synthesis of Fluorescent 2‐(Pyrano[3,2‐c]chromene‐5‐yl)Acetic Acids From Chromone‐Containing Acrylic Acids. / Рязанцев, Михаил Николаевич; Ефимов, Сергей; Чернов, Никита; Панов, Максим Сергеевич; Николаев, Дмитрий Михайлович; Шутов, Роман; Яковлев, Игорь .
в: Journal of Heterocyclic Chemistry, Том 62, № 8, 06.07.2025, стр. 546-553.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Synthesis of Fluorescent 2‐(Pyrano[3,2‐c]chromene‐5‐yl)Acetic Acids From Chromone‐Containing Acrylic Acids
AU - Рязанцев, Михаил Николаевич
AU - Ефимов, Сергей
AU - Чернов, Никита
AU - Панов, Максим Сергеевич
AU - Николаев, Дмитрий Михайлович
AU - Шутов, Роман
AU - Яковлев, Игорь
PY - 2025/7/6
Y1 - 2025/7/6
N2 - We have developed a convenient method for the synthesis of 2-(pyrano[3,2-c]chromen-5-yl)acetic acids and their derivatives. The synthetic approach is based on the ANRORC reaction of chromone-containing acrylic acids and ethyl cyanoacetate. The features of the method are (a) simple reaction conditions (ethanol, 20°C–25°C, triethylamine as catalyst), (b) non-chromatographic isolation of products, and (c) high yields (up to 95%). The resulting pyrano[3,2-c]chromenes have intense fluorescence in the yellow-green region of the spectrum (492–554 nm) and demonstrate large Stokes shifts (up to 6300 cm−1).
AB - We have developed a convenient method for the synthesis of 2-(pyrano[3,2-c]chromen-5-yl)acetic acids and their derivatives. The synthetic approach is based on the ANRORC reaction of chromone-containing acrylic acids and ethyl cyanoacetate. The features of the method are (a) simple reaction conditions (ethanol, 20°C–25°C, triethylamine as catalyst), (b) non-chromatographic isolation of products, and (c) high yields (up to 95%). The resulting pyrano[3,2-c]chromenes have intense fluorescence in the yellow-green region of the spectrum (492–554 nm) and demonstrate large Stokes shifts (up to 6300 cm−1).
KW - chromone
KW - cyclization
KW - fluorescence
KW - heterocycles
KW - nucleophilic addition
UR - https://www.mendeley.com/catalogue/0d572b8f-bb73-34d3-ae8e-2a6dfd8b5c93/
U2 - 10.1002/jhet.70008
DO - 10.1002/jhet.70008
M3 - Article
VL - 62
SP - 546
EP - 553
JO - Journal of Heterocyclic Chemistry
JF - Journal of Heterocyclic Chemistry
SN - 0022-152X
IS - 8
ER -
ID: 142897636