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Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review). / Пронина, Юлия ; Тегляй, Л.А.; Поняев, Александр; Петров, М.Л.; Бойцов, Виталий Михайлович; Степаков, Александр Владимирович.

In: Russian Journal of General Chemistry, Vol. 94, No. 1, 2024, p. 1-44.

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

Harvard

Пронина, Ю, Тегляй, ЛА, Поняев, А, Петров, МЛ, Бойцов, ВМ & Степаков, АВ 2024, 'Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review).', Russian Journal of General Chemistry, vol. 94, no. 1, pp. 1-44. https://doi.org/10.1134/S1070363224010018, https://doi.org/10.1134/S1070363224010018

APA

Пронина, Ю., Тегляй, Л. А., Поняев, А., Петров, М. Л., Бойцов, В. М., & Степаков, А. В. (2024). Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review). Russian Journal of General Chemistry, 94(1), 1-44. https://doi.org/10.1134/S1070363224010018, https://doi.org/10.1134/S1070363224010018

Vancouver

Пронина Ю, Тегляй ЛА, Поняев А, Петров МЛ, Бойцов ВМ, Степаков АВ. Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review). Russian Journal of General Chemistry. 2024;94(1):1-44. https://doi.org/10.1134/S1070363224010018, https://doi.org/10.1134/S1070363224010018

Author

Пронина, Юлия ; Тегляй, Л.А. ; Поняев, Александр ; Петров, М.Л. ; Бойцов, Виталий Михайлович ; Степаков, Александр Владимирович. / Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review). In: Russian Journal of General Chemistry. 2024 ; Vol. 94, No. 1. pp. 1-44.

BibTeX

@article{8ef171ec39f2464796af27b10750f706,
title = "Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review).",
abstract = "Abstract: One of the promising directions in 1,3-dipolar cycloaddition is the implementation of these reactions under organocatalysis conditions, which makes it possible to achieve not only high products yields, but also complete stereocontrol of the process. The presented review analyzes data published over the past 5 years according to the types of 1,3-dipoles involved into reactions. In a number of cases, the mechanisms of 1,3-dipolar cycloaddition reactions occurring in the presence of organocatalysts are discussed in detail.",
keywords = "1,3-dipolar cycloaddition, azides, azomethine imines, azomethine ylides, nitrones, organocatalysis, stereoselectivity",
author = "Юлия Пронина and Л.А. Тегляй and Александр Поняев and М.Л. Петров and Бойцов, {Виталий Михайлович} and Степаков, {Александр Владимирович}",
year = "2024",
doi = "10.1134/S1070363224010018",
language = "English",
volume = "94",
pages = "1--44",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "1",

}

RIS

TY - JOUR

T1 - Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review).

AU - Пронина, Юлия

AU - Тегляй, Л.А.

AU - Поняев, Александр

AU - Петров, М.Л.

AU - Бойцов, Виталий Михайлович

AU - Степаков, Александр Владимирович

PY - 2024

Y1 - 2024

N2 - Abstract: One of the promising directions in 1,3-dipolar cycloaddition is the implementation of these reactions under organocatalysis conditions, which makes it possible to achieve not only high products yields, but also complete stereocontrol of the process. The presented review analyzes data published over the past 5 years according to the types of 1,3-dipoles involved into reactions. In a number of cases, the mechanisms of 1,3-dipolar cycloaddition reactions occurring in the presence of organocatalysts are discussed in detail.

AB - Abstract: One of the promising directions in 1,3-dipolar cycloaddition is the implementation of these reactions under organocatalysis conditions, which makes it possible to achieve not only high products yields, but also complete stereocontrol of the process. The presented review analyzes data published over the past 5 years according to the types of 1,3-dipoles involved into reactions. In a number of cases, the mechanisms of 1,3-dipolar cycloaddition reactions occurring in the presence of organocatalysts are discussed in detail.

KW - 1,3-dipolar cycloaddition

KW - azides

KW - azomethine imines

KW - azomethine ylides

KW - nitrones

KW - organocatalysis

KW - stereoselectivity

UR - https://www.mendeley.com/catalogue/d14facd5-e124-3735-9aff-0c5c17a452c0/

U2 - 10.1134/S1070363224010018

DO - 10.1134/S1070363224010018

M3 - Review article

VL - 94

SP - 1

EP - 44

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 1

ER -

ID: 124623046