Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions

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Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions. / Molchanov, A. P.; Efremova, M. M.; Kuznetsov, M. A.

In: Russian Chemical Bulletin, Vol. 71, No. 4, 01.04.2022, p. 620-650.

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

BibTeX

@article{c3399528542c4ab78da11be06ac2576f,

title = "Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions",

abstract = "The review considers the main results of the cycloaddition reactions involving cyclopropenes and methylenecyclopropanes, the compounds bearing strained three-membered rings and, respectively, endo- and exocyclic double bonds. The main attention is focused on the reactions of these compounds with 1,3-dipoles (nitrones, azomethine imines, azomethine ylides, carbonyl ylides, etc.), which gave complex heterocyclic systems with high regio- and stereoselectivity.",

keywords = "azomethine imines, azomethine ylides, carbonyl ylides, cyclopropenes, diazo compounds, dipolar cycloaddition, methylenecyclopropanes, nitrones",

author = "Molchanov, {A. P.} and Efremova, {M. M.} and Kuznetsov, {M. A.}",

note = "Publisher Copyright: {\textcopyright} 2022, Springer Science+Business Media LLC.",

year = "2022",

month = apr,

day = "1",

doi = "10.1007/s11172-022-3460-z",

language = "English",

volume = "71",

pages = "620--650",

journal = "Russian Chemical Bulletin",

issn = "1066-5285",

publisher = "Springer Nature",

number = "4",

}

RIS

TY - JOUR

T1 - Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions

AU - Molchanov, A. P.

AU - Efremova, M. M.

AU - Kuznetsov, M. A.

PY - 2022/4/1

Y1 - 2022/4/1

N2 - The review considers the main results of the cycloaddition reactions involving cyclopropenes and methylenecyclopropanes, the compounds bearing strained three-membered rings and, respectively, endo- and exocyclic double bonds. The main attention is focused on the reactions of these compounds with 1,3-dipoles (nitrones, azomethine imines, azomethine ylides, carbonyl ylides, etc.), which gave complex heterocyclic systems with high regio- and stereoselectivity.

AB - The review considers the main results of the cycloaddition reactions involving cyclopropenes and methylenecyclopropanes, the compounds bearing strained three-membered rings and, respectively, endo- and exocyclic double bonds. The main attention is focused on the reactions of these compounds with 1,3-dipoles (nitrones, azomethine imines, azomethine ylides, carbonyl ylides, etc.), which gave complex heterocyclic systems with high regio- and stereoselectivity.

KW - azomethine imines

KW - azomethine ylides

KW - carbonyl ylides

KW - cyclopropenes

KW - diazo compounds

KW - dipolar cycloaddition

KW - methylenecyclopropanes

KW - nitrones

UR - http://www.scopus.com/inward/record.url?scp=85128849338&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/18dc67c1-14c3-35c2-bf56-88fc320a02d8/

U2 - 10.1007/s11172-022-3460-z

DO - 10.1007/s11172-022-3460-z

M3 - Review article

AN - SCOPUS:85128849338

VL - 71

SP - 620

EP - 650

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 4

ER -

ID: 96242286