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Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates. / Svintsitskaya, Nataly I.; Dogadina, Albina V.; Starova, Galina L.; Trifonov, Rostislav E.

в: Tetrahedron Letters, Том 55, № 39, 2014, стр. 5381-5385.

Результаты исследований: Научные публикации в периодических изданиях › статья

Harvard

Svintsitskaya, NI, Dogadina, AV, Starova, GL & Trifonov, RE 2014, 'Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates', Tetrahedron Letters, Том. 55, № 39, стр. 5381-5385. https://doi.org/10.1016/j.tetlet.2014.08.018

APA

Svintsitskaya, N. I., Dogadina, A. V., Starova, G. L., & Trifonov, R. E. (2014). Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates. Tetrahedron Letters, 55(39), 5381-5385. https://doi.org/10.1016/j.tetlet.2014.08.018

Vancouver

Svintsitskaya NI, Dogadina AV, Starova GL, Trifonov RE. Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates. Tetrahedron Letters. 2014;55(39):5381-5385. https://doi.org/10.1016/j.tetlet.2014.08.018

Author

Svintsitskaya, Nataly I. ; Dogadina, Albina V. ; Starova, Galina L. ; Trifonov, Rostislav E. / Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates. в: Tetrahedron Letters. 2014 ; Том 55, № 39. стр. 5381-5385.

BibTeX

@article{2df6c041b138435bbf3030ffa49da65d,
title = "Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates",
abstract = "Addition of 5-substituted tetrazoles to dimethyl [(N,N-diisopropylamino)ethynyl]phosphonate proceeds regio- and stereoselectively to yield (Z)[2-diisopropylamino-2-(tetrazolyl)vinyl]phosphonic acid dimethyl esters. The Z-configuration of the products was confirmed by H-1 NMR spectroscopy and single-crystal X-ray diffraction. The reactions occur via nucleophilic attack of tetrazole involving predominantly the N-1 atom of the tetrazole ring. (C) 2014 Elsevier Ltd. All rights reserved.",
author = "Svintsitskaya, {Nataly I.} and Dogadina, {Albina V.} and Starova, {Galina L.} and Trifonov, {Rostislav E.}",
year = "2014",
doi = "10.1016/j.tetlet.2014.08.018",
language = "English",
volume = "55",
pages = "5381--5385",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",
number = "39",

}

RIS

TY - JOUR

T1 - Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates

AU - Svintsitskaya, Nataly I.

AU - Dogadina, Albina V.

AU - Starova, Galina L.

AU - Trifonov, Rostislav E.

PY - 2014

Y1 - 2014

N2 - Addition of 5-substituted tetrazoles to dimethyl [(N,N-diisopropylamino)ethynyl]phosphonate proceeds regio- and stereoselectively to yield (Z)[2-diisopropylamino-2-(tetrazolyl)vinyl]phosphonic acid dimethyl esters. The Z-configuration of the products was confirmed by H-1 NMR spectroscopy and single-crystal X-ray diffraction. The reactions occur via nucleophilic attack of tetrazole involving predominantly the N-1 atom of the tetrazole ring. (C) 2014 Elsevier Ltd. All rights reserved.

AB - Addition of 5-substituted tetrazoles to dimethyl [(N,N-diisopropylamino)ethynyl]phosphonate proceeds regio- and stereoselectively to yield (Z)[2-diisopropylamino-2-(tetrazolyl)vinyl]phosphonic acid dimethyl esters. The Z-configuration of the products was confirmed by H-1 NMR spectroscopy and single-crystal X-ray diffraction. The reactions occur via nucleophilic attack of tetrazole involving predominantly the N-1 atom of the tetrazole ring. (C) 2014 Elsevier Ltd. All rights reserved.

U2 - 10.1016/j.tetlet.2014.08.018

DO - 10.1016/j.tetlet.2014.08.018

M3 - Article

VL - 55

SP - 5381

EP - 5385

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 39

ER -

ID: 7010812