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5-Phenyl-2H-tetrazol-2-ylmethyl Ketones in the Synthesis of Tetrazolylalkanols and Tetrazolyl(hydroxy)alkylphosphonates. / Krylov, A.S.; Dogadina, A.V.; Trifonov, R.E.

In: Russian Journal of Organic Chemistry, Vol. 50, No. 6, 2014, p. 892-894.

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Krylov, A.S. ; Dogadina, A.V. ; Trifonov, R.E. / 5-Phenyl-2H-tetrazol-2-ylmethyl Ketones in the Synthesis of Tetrazolylalkanols and Tetrazolyl(hydroxy)alkylphosphonates. In: Russian Journal of Organic Chemistry. 2014 ; Vol. 50, No. 6. pp. 892-894.

BibTeX

@article{896de9fe20ad41a488fd61a6eb9be7c9,
title = "5-Phenyl-2H-tetrazol-2-ylmethyl Ketones in the Synthesis of Tetrazolylalkanols and Tetrazolyl(hydroxy)alkylphosphonates",
abstract = "The reduction of 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-one and 1-phenyl-2-(5-phenyl-2H-tetrazol- 2-yl)ethanone with sodium tetrahydridoborate gave 1-(5-phenyl-2H-tetrazol-2-yl)propan-1-ol and 1-phenyl-2- (5-phenyl-2H-tetrazol-2-yl)ethanol, respectively. Only 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-one was reduced with baker{\textquoteright}s yeast with an appreciable yield. 1-(5-Phenyl-2H-tetrazol-2-yl)propan-2-one and 1-phenyl-2-(5- phenyl-2H-tetrazol-2-yl)ethanone reacted with diethyl phosphonate in the presence of potassium fluoride to produce the corresponding diethyl [hydroxy(5-phenyl-2H-tetrazol-2-yl)alkyl]phosphonates.",
author = "A.S. Krylov and A.V. Dogadina and R.E. Trifonov",
year = "2014",
doi = "10.1134/S1070428014060219",
language = "English",
volume = "50",
pages = "892--894",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "6",

}

RIS

TY - JOUR

T1 - 5-Phenyl-2H-tetrazol-2-ylmethyl Ketones in the Synthesis of Tetrazolylalkanols and Tetrazolyl(hydroxy)alkylphosphonates

AU - Krylov, A.S.

AU - Dogadina, A.V.

AU - Trifonov, R.E.

PY - 2014

Y1 - 2014

N2 - The reduction of 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-one and 1-phenyl-2-(5-phenyl-2H-tetrazol- 2-yl)ethanone with sodium tetrahydridoborate gave 1-(5-phenyl-2H-tetrazol-2-yl)propan-1-ol and 1-phenyl-2- (5-phenyl-2H-tetrazol-2-yl)ethanol, respectively. Only 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-one was reduced with baker’s yeast with an appreciable yield. 1-(5-Phenyl-2H-tetrazol-2-yl)propan-2-one and 1-phenyl-2-(5- phenyl-2H-tetrazol-2-yl)ethanone reacted with diethyl phosphonate in the presence of potassium fluoride to produce the corresponding diethyl [hydroxy(5-phenyl-2H-tetrazol-2-yl)alkyl]phosphonates.

AB - The reduction of 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-one and 1-phenyl-2-(5-phenyl-2H-tetrazol- 2-yl)ethanone with sodium tetrahydridoborate gave 1-(5-phenyl-2H-tetrazol-2-yl)propan-1-ol and 1-phenyl-2- (5-phenyl-2H-tetrazol-2-yl)ethanol, respectively. Only 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-one was reduced with baker’s yeast with an appreciable yield. 1-(5-Phenyl-2H-tetrazol-2-yl)propan-2-one and 1-phenyl-2-(5- phenyl-2H-tetrazol-2-yl)ethanone reacted with diethyl phosphonate in the presence of potassium fluoride to produce the corresponding diethyl [hydroxy(5-phenyl-2H-tetrazol-2-yl)alkyl]phosphonates.

U2 - 10.1134/S1070428014060219

DO - 10.1134/S1070428014060219

M3 - Article

VL - 50

SP - 892

EP - 894

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 6

ER -

ID: 7013232