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A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides. / Zhmurov, Petr A.; Ushakov, Pavel Yu; Novikov, Roman A.; Sukhorukov, Alexey Yu; Ioffe, Sema L.

In: Synlett, Vol. 29, No. 14, 01.01.2018, p. 1871-1874.

Research output: Contribution to journal › Article › peer-review

Harvard

Zhmurov, PA, Ushakov, PY, Novikov, RA, Sukhorukov, AY & Ioffe, SL 2018, 'A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides', Synlett, vol. 29, no. 14, pp. 1871-1874. https://doi.org/10.1055/s-0037-1610213

APA

Zhmurov, P. A., Ushakov, P. Y., Novikov, R. A., Sukhorukov, A. Y., & Ioffe, S. L. (2018). A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides. Synlett, 29(14), 1871-1874. https://doi.org/10.1055/s-0037-1610213

Vancouver

Zhmurov PA, Ushakov PY, Novikov RA, Sukhorukov AY, Ioffe SL. A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides. Synlett. 2018 Jan 1;29(14):1871-1874. https://doi.org/10.1055/s-0037-1610213

Author

Zhmurov, Petr A. ; Ushakov, Pavel Yu ; Novikov, Roman A. ; Sukhorukov, Alexey Yu ; Ioffe, Sema L. / A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides. In: Synlett. 2018 ; Vol. 29, No. 14. pp. 1871-1874.

BibTeX

@article{e3301e2d2e444f89943bc18249015d58,
title = "A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides",
abstract = "A novel strategy for the synthesis of stereochemically defined 3,4,5-trisubstituted 2-pyrrolidones was developed. The suggested approach involves reductive domino-type recyclization of 3-aminomethyl-substituted isoxazolines as a key stage. The latter are prepared via α-C-H functionalization of readily available isoxazoline-N-oxides.",
keywords = "2-pyrrolidones, azides, C-H functionalization, isoxazolines, reduction",
author = "Zhmurov, {Petr A.} and Ushakov, {Pavel Yu} and Novikov, {Roman A.} and Sukhorukov, {Alexey Yu} and Ioffe, {Sema L.}",
year = "2018",
month = jan,
day = "1",
doi = "10.1055/s-0037-1610213",
language = "English",
volume = "29",
pages = "1871--1874",
journal = "Synlett",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "14",

}

RIS

TY - JOUR

T1 - A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides

AU - Zhmurov, Petr A.

AU - Ushakov, Pavel Yu

AU - Novikov, Roman A.

AU - Sukhorukov, Alexey Yu

AU - Ioffe, Sema L.

PY - 2018/1/1

Y1 - 2018/1/1

N2 - A novel strategy for the synthesis of stereochemically defined 3,4,5-trisubstituted 2-pyrrolidones was developed. The suggested approach involves reductive domino-type recyclization of 3-aminomethyl-substituted isoxazolines as a key stage. The latter are prepared via α-C-H functionalization of readily available isoxazoline-N-oxides.

AB - A novel strategy for the synthesis of stereochemically defined 3,4,5-trisubstituted 2-pyrrolidones was developed. The suggested approach involves reductive domino-type recyclization of 3-aminomethyl-substituted isoxazolines as a key stage. The latter are prepared via α-C-H functionalization of readily available isoxazoline-N-oxides.

KW - 2-pyrrolidones

KW - azides

KW - C-H functionalization

KW - isoxazolines

KW - reduction

UR - http://www.scopus.com/inward/record.url?scp=85051941775&partnerID=8YFLogxK

U2 - 10.1055/s-0037-1610213

DO - 10.1055/s-0037-1610213

M3 - Article

AN - SCOPUS:85051941775

VL - 29

SP - 1871

EP - 1874

JO - Synlett

JF - Synlett

SN - 0936-5214

IS - 14

ER -

ID: 51899879