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Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles (review). / Lobanov, P.S.; Dar'In, D.V.

In: Chemistry of Heterocyclic Compounds, Vol. 49, No. 4, 2013, p. 507-528.

Research output: Contribution to journal › Review article

Harvard

Lobanov, PS & Dar'In, DV 2013, 'Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles (review)', Chemistry of Heterocyclic Compounds, vol. 49, no. 4, pp. 507-528. https://doi.org/10.1007/s10593-013-1277-2

APA

Lobanov, P. S., & Dar'In, D. V. (2013). Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles (review). Chemistry of Heterocyclic Compounds, 49(4), 507-528. https://doi.org/10.1007/s10593-013-1277-2

Vancouver

Lobanov PS, Dar'In DV. Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles (review). Chemistry of Heterocyclic Compounds. 2013;49(4):507-528. https://doi.org/10.1007/s10593-013-1277-2

Author

Lobanov, P.S. ; Dar'In, D.V. / Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles (review). In: Chemistry of Heterocyclic Compounds. 2013 ; Vol. 49, No. 4. pp. 507-528.

BibTeX

@article{71ef97da40ab4cd4b82a6fb2a15da1fa,
title = "Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles (review)",
abstract = "Published information on heterocyclizations involving acetamidines and acetamidoximes substituted at the alpha-position with an electron-withdrawing group is reviewed, where these starting materials have been used in the synthesis of 2-aminoazaheterocycles (2-aminopyridines, 2-aminopyrroles, and 2-aminoazirines). In such reactions the alpha-carbon atom of the amidine or amidoxime is included in the ring of the obtained heterocycle.",
author = "P.S. Lobanov and D.V. Dar'In",
year = "2013",
doi = "10.1007/s10593-013-1277-2",
language = "English",
volume = "49",
pages = "507--528",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer Nature",
number = "4",

}

RIS

TY - JOUR

T1 - Acetamidines and acetamidoximes containing an electron-withdrawing group at the α-carbon atom: their use in the synthesis of nitrogen heterocycles (review)

AU - Lobanov, P.S.

AU - Dar'In, D.V.

PY - 2013

Y1 - 2013

N2 - Published information on heterocyclizations involving acetamidines and acetamidoximes substituted at the alpha-position with an electron-withdrawing group is reviewed, where these starting materials have been used in the synthesis of 2-aminoazaheterocycles (2-aminopyridines, 2-aminopyrroles, and 2-aminoazirines). In such reactions the alpha-carbon atom of the amidine or amidoxime is included in the ring of the obtained heterocycle.

AB - Published information on heterocyclizations involving acetamidines and acetamidoximes substituted at the alpha-position with an electron-withdrawing group is reviewed, where these starting materials have been used in the synthesis of 2-aminoazaheterocycles (2-aminopyridines, 2-aminopyrroles, and 2-aminoazirines). In such reactions the alpha-carbon atom of the amidine or amidoxime is included in the ring of the obtained heterocycle.

U2 - 10.1007/s10593-013-1277-2

DO - 10.1007/s10593-013-1277-2

M3 - Review article

VL - 49

SP - 507

EP - 528

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 4

ER -

ID: 7378954