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Approaches to the synthesis of heterocyclic C-nucleosides. / Mukhin, E. M.; Savateev, K. V.; Rusinov, V. L.
In: Russian Chemical Bulletin, Vol. 72, No. 2, 01.02.2023, p. 425-481.

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

Harvard

Mukhin, EM, Savateev, KV & Rusinov, VL 2023, 'Approaches to the synthesis of heterocyclic C-nucleosides', Russian Chemical Bulletin, vol. 72, no. 2, pp. 425-481. https://doi.org/10.1007/s11172-023-3810-1

APA

Mukhin, E. M., Savateev, K. V., & Rusinov, V. L. (2023). Approaches to the synthesis of heterocyclic C-nucleosides. Russian Chemical Bulletin, 72(2), 425-481. https://doi.org/10.1007/s11172-023-3810-1

Vancouver

Mukhin EM, Savateev KV, Rusinov VL. Approaches to the synthesis of heterocyclic C-nucleosides. Russian Chemical Bulletin. 2023 Feb 1;72(2):425-481. doi: 10.1007/s11172-023-3810-1

Author

Mukhin, E. M. ; Savateev, K. V. ; Rusinov, V. L. / Approaches to the synthesis of heterocyclic C-nucleosides. In: Russian Chemical Bulletin. 2023 ; Vol. 72, No. 2. pp. 425-481.

BibTeX

@article{a3da097b60c24c3e95f93f239a56dfbb,
title = "Approaches to the synthesis of heterocyclic C-nucleosides",
abstract = "This review is focused on the synthetic strategies to heterocyclic C-nucleosides and covers the literature from 2011 to 2021. The main attention is paid to the following three approaches: the direct C—C coupling of a carbohydrate moiety with a preformed aglycon unit, the construction of a (pseudo)sugar residue on a pre-formed aglycon, and the construction of an aglycon on a pre-formed (pseudo)sugar. In each Section, the literature data are categorized in terms of the size of aglycon from simple to complex, the advantages and drawbacks of the reviewed approaches are discussed.",
author = "Mukhin, {E. M.} and Savateev, {K. V.} and Rusinov, {V. L.}",
year = "2023",
month = feb,
day = "1",
doi = "10.1007/s11172-023-3810-1",
language = "English",
volume = "72",
pages = "425--481",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "2",

}

RIS

TY - JOUR

T1 - Approaches to the synthesis of heterocyclic C-nucleosides

AU - Mukhin, E. M.

AU - Savateev, K. V.

AU - Rusinov, V. L.

PY - 2023/2/1

Y1 - 2023/2/1

N2 - This review is focused on the synthetic strategies to heterocyclic C-nucleosides and covers the literature from 2011 to 2021. The main attention is paid to the following three approaches: the direct C—C coupling of a carbohydrate moiety with a preformed aglycon unit, the construction of a (pseudo)sugar residue on a pre-formed aglycon, and the construction of an aglycon on a pre-formed (pseudo)sugar. In each Section, the literature data are categorized in terms of the size of aglycon from simple to complex, the advantages and drawbacks of the reviewed approaches are discussed.

AB - This review is focused on the synthetic strategies to heterocyclic C-nucleosides and covers the literature from 2011 to 2021. The main attention is paid to the following three approaches: the direct C—C coupling of a carbohydrate moiety with a preformed aglycon unit, the construction of a (pseudo)sugar residue on a pre-formed aglycon, and the construction of an aglycon on a pre-formed (pseudo)sugar. In each Section, the literature data are categorized in terms of the size of aglycon from simple to complex, the advantages and drawbacks of the reviewed approaches are discussed.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85153314645

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000989930300010

U2 - 10.1007/s11172-023-3810-1

DO - 10.1007/s11172-023-3810-1

M3 - Review article

VL - 72

SP - 425

EP - 481

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 2

ER -

ID: 38496936