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Alkylation of 5-substituted NH-tetrazoles by alcohols in the superacid CF3SO3H. / Lisakova, A.D.; Ryabukhin, D.S.; Trifonov, R.E.; Ostrovskii, V.A.; Vasilyev, A.V.

In: Tetrahedron Letters, Vol. 56, No. 50, 2015, p. 7020-7023.

Research output: Contribution to journal › Article

Harvard

Lisakova, AD, Ryabukhin, DS, Trifonov, RE, Ostrovskii, VA & Vasilyev, AV 2015, 'Alkylation of 5-substituted NH-tetrazoles by alcohols in the superacid CF3SO3H', Tetrahedron Letters, vol. 56, no. 50, pp. 7020-7023. https://doi.org/10.1016/j.tetlet.2015.11.005

APA

Lisakova, A. D., Ryabukhin, D. S., Trifonov, R. E., Ostrovskii, V. A., & Vasilyev, A. V. (2015). Alkylation of 5-substituted NH-tetrazoles by alcohols in the superacid CF3SO3H. Tetrahedron Letters, 56(50), 7020-7023. https://doi.org/10.1016/j.tetlet.2015.11.005

Vancouver

Lisakova AD, Ryabukhin DS, Trifonov RE, Ostrovskii VA, Vasilyev AV. Alkylation of 5-substituted NH-tetrazoles by alcohols in the superacid CF3SO3H. Tetrahedron Letters. 2015;56(50):7020-7023. https://doi.org/10.1016/j.tetlet.2015.11.005

Author

Lisakova, A.D. ; Ryabukhin, D.S. ; Trifonov, R.E. ; Ostrovskii, V.A. ; Vasilyev, A.V. / Alkylation of 5-substituted NH-tetrazoles by alcohols in the superacid CF3SO3H. In: Tetrahedron Letters. 2015 ; Vol. 56, No. 50. pp. 7020-7023.

BibTeX

@article{8540f6ad87df4876a2ab2627bb40d055,
title = "Alkylation of 5-substituted NH-tetrazoles by alcohols in the superacid CF3SO3H",
abstract = "{\textcopyright} 2015 Elsevier Ltd.Reactions of 5-substituted NH-tetrazoles with alcohols in the superacid CF3SO3H have been studied. Both the structure of the tetrazole and the nature of alcohol were found to dramatically influence the selectivity of the reaction and yields of products. Tetrazoles bearing phenyl, electron-donating aryl, or benzyl groups at the 5-position, have been alkylated using various alcohols (including MeOH and EtOH) in CF3SO3H upon heating at 60 °C for 0.3-12 h to afford 2-alkyl-2H-tetrazoles in 30-98% yields.",
author = "A.D. Lisakova and D.S. Ryabukhin and R.E. Trifonov and V.A. Ostrovskii and A.V. Vasilyev",
year = "2015",
doi = "10.1016/j.tetlet.2015.11.005",
language = "English",
volume = "56",
pages = "7020--7023",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",
number = "50",

}

RIS

TY - JOUR

T1 - Alkylation of 5-substituted NH-tetrazoles by alcohols in the superacid CF3SO3H

AU - Lisakova, A.D.

AU - Ryabukhin, D.S.

AU - Trifonov, R.E.

AU - Ostrovskii, V.A.

AU - Vasilyev, A.V.

PY - 2015

Y1 - 2015

N2 - © 2015 Elsevier Ltd.Reactions of 5-substituted NH-tetrazoles with alcohols in the superacid CF3SO3H have been studied. Both the structure of the tetrazole and the nature of alcohol were found to dramatically influence the selectivity of the reaction and yields of products. Tetrazoles bearing phenyl, electron-donating aryl, or benzyl groups at the 5-position, have been alkylated using various alcohols (including MeOH and EtOH) in CF3SO3H upon heating at 60 °C for 0.3-12 h to afford 2-alkyl-2H-tetrazoles in 30-98% yields.

AB - © 2015 Elsevier Ltd.Reactions of 5-substituted NH-tetrazoles with alcohols in the superacid CF3SO3H have been studied. Both the structure of the tetrazole and the nature of alcohol were found to dramatically influence the selectivity of the reaction and yields of products. Tetrazoles bearing phenyl, electron-donating aryl, or benzyl groups at the 5-position, have been alkylated using various alcohols (including MeOH and EtOH) in CF3SO3H upon heating at 60 °C for 0.3-12 h to afford 2-alkyl-2H-tetrazoles in 30-98% yields.

U2 - 10.1016/j.tetlet.2015.11.005

DO - 10.1016/j.tetlet.2015.11.005

M3 - Article

VL - 56

SP - 7020

EP - 7023

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 50

ER -

ID: 3979051