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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 изданияхстатьяРецензирование

Harvard

Рязанцев, МН, Ефимов, С, Чернов, Н, Панов, МС, Николаев, ДМ, Шутов, Р & Яковлев, И 2025, 'Synthesis of Fluorescent 2‐(Pyrano[3,2‐c]chromene‐5‐yl)Acetic Acids From Chromone‐Containing Acrylic Acids', Journal of Heterocyclic Chemistry, Том. 62, № 8, стр. 546-553. https://doi.org/10.1002/jhet.70008

APA

Vancouver

Author

Рязанцев, Михаил Николаевич ; Ефимов, Сергей ; Чернов, Никита ; Панов, Максим Сергеевич ; Николаев, Дмитрий Михайлович ; Шутов, Роман ; Яковлев, Игорь . / Synthesis of Fluorescent 2‐(Pyrano[3,2‐c]chromene‐5‐yl)Acetic Acids From Chromone‐Containing Acrylic Acids. в: Journal of Heterocyclic Chemistry. 2025 ; Том 62, № 8. стр. 546-553.

BibTeX

@article{4e785d6e023e4110831dd8647b816dd5,
title = "Synthesis of Fluorescent 2‐(Pyrano[3,2‐c]chromene‐5‐yl)Acetic Acids From Chromone‐Containing Acrylic Acids",
abstract = "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).",
keywords = "chromone, cyclization, fluorescence, heterocycles, nucleophilic addition",
author = "Рязанцев, {Михаил Николаевич} and Сергей Ефимов and Никита Чернов and Панов, {Максим Сергеевич} and Николаев, {Дмитрий Михайлович} and Роман Шутов and Игорь Яковлев",
year = "2025",
month = jul,
day = "6",
doi = "10.1002/jhet.70008",
language = "English",
volume = "62",
pages = " 546--553",
journal = "Journal of Heterocyclic Chemistry",
issn = "0022-152X",
publisher = "Wiley-Blackwell",
number = "8",

}

RIS

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