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Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone. / Sosnovskikh, V. Ya.
In: Russian Chemical Bulletin, Vol. 71, No. 11, 01.11.2022, p. 2285-2309.

Research output: Contribution to journal › Review article › peer-review

Harvard

Sosnovskikh, VY 2022, 'Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone', Russian Chemical Bulletin, vol. 71, no. 11, pp. 2285-2309. https://doi.org/10.1007/s11172-022-3658-0

APA

Sosnovskikh, V. Y. (2022). Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone. Russian Chemical Bulletin, 71(11), 2285-2309. https://doi.org/10.1007/s11172-022-3658-0

Vancouver

Sosnovskikh VY. Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone. Russian Chemical Bulletin. 2022 Nov 1;71(11):2285-2309. doi: 10.1007/s11172-022-3658-0

Author

Sosnovskikh, V. Ya. / Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone. In: Russian Chemical Bulletin. 2022 ; Vol. 71, No. 11. pp. 2285-2309.

BibTeX

@article{2c24047f16e74783850b4da1e61a38ba,
title = "Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone",
abstract = "The review is devoted to 2,3-heteroannelated chromones. The methods of their synthesis, unlike 2,3-heterothiochromones, were not generalized and analyzed. The systematization of synthetic approaches to these compounds is based on the structure of the used substrate. An analysis of the literature data shows that the most valuable starting substances that are most frequently used for the synthesis of xanthone heteroanalogues include 3-mono- and 2,3-difunctionalized chromones, as well as such precursors of the chromone system as 1-oxohetaryl-2-hydroxy(halo)arenes. Of all the 2,3-heterochromones described in this review, the chemistry of chromonopyrazoles is developed to a highest extent. {\textcopyright} 2022, Springer Science+Business Media LLC.",
author = "Sosnovskikh, {V. Ya.}",
year = "2022",
month = nov,
day = "1",
doi = "10.1007/s11172-022-3658-0",
language = "English",
volume = "71",
pages = "2285--2309",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "11",

}

RIS

TY - JOUR

T1 - Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone

AU - Sosnovskikh, V. Ya.

PY - 2022/11/1

Y1 - 2022/11/1

N2 - The review is devoted to 2,3-heteroannelated chromones. The methods of their synthesis, unlike 2,3-heterothiochromones, were not generalized and analyzed. The systematization of synthetic approaches to these compounds is based on the structure of the used substrate. An analysis of the literature data shows that the most valuable starting substances that are most frequently used for the synthesis of xanthone heteroanalogues include 3-mono- and 2,3-difunctionalized chromones, as well as such precursors of the chromone system as 1-oxohetaryl-2-hydroxy(halo)arenes. Of all the 2,3-heterochromones described in this review, the chemistry of chromonopyrazoles is developed to a highest extent. © 2022, Springer Science+Business Media LLC.

AB - The review is devoted to 2,3-heteroannelated chromones. The methods of their synthesis, unlike 2,3-heterothiochromones, were not generalized and analyzed. The systematization of synthetic approaches to these compounds is based on the structure of the used substrate. An analysis of the literature data shows that the most valuable starting substances that are most frequently used for the synthesis of xanthone heteroanalogues include 3-mono- and 2,3-difunctionalized chromones, as well as such precursors of the chromone system as 1-oxohetaryl-2-hydroxy(halo)arenes. Of all the 2,3-heterochromones described in this review, the chemistry of chromonopyrazoles is developed to a highest extent. © 2022, Springer Science+Business Media LLC.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85144297611

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000921286500001

U2 - 10.1007/s11172-022-3658-0

DO - 10.1007/s11172-022-3658-0

M3 - Review article

VL - 71

SP - 2285

EP - 2309

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 11

ER -

ID: 33184144