(RS)-benzyl mandelateCitation formats

Standard

(RS)-benzyl mandelate. / Mughal, Robila K.; Pritchard, Robin G.; Davey, Roger J.

In: Acta Crystallographica Section E: Structure Reports Online, Vol. 60, No. 11, 11.2004, p. o1984-o1986.

Research output: Contribution to journalArticle

Harvard

Mughal, RK, Pritchard, RG & Davey, RJ 2004, '(RS)-benzyl mandelate', Acta Crystallographica Section E: Structure Reports Online, vol. 60, no. 11, pp. o1984-o1986. https://doi.org/10.1107/S1600536804025024

APA

Mughal, R. K., Pritchard, R. G., & Davey, R. J. (2004). (RS)-benzyl mandelate. Acta Crystallographica Section E: Structure Reports Online, 60(11), o1984-o1986. https://doi.org/10.1107/S1600536804025024

Vancouver

Mughal RK, Pritchard RG, Davey RJ. (RS)-benzyl mandelate. Acta Crystallographica Section E: Structure Reports Online. 2004 Nov;60(11):o1984-o1986. https://doi.org/10.1107/S1600536804025024

Author

Mughal, Robila K. ; Pritchard, Robin G. ; Davey, Roger J. / (RS)-benzyl mandelate. In: Acta Crystallographica Section E: Structure Reports Online. 2004 ; Vol. 60, No. 11. pp. o1984-o1986.

Bibtex

@article{11dba6119d2042849b6334b89189c2f2,
title = "(RS)-benzyl mandelate",
abstract = "A benzyl ester of mandelic acid, C15H14O 3, was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen-bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality. {\circledC} 2004 International Union of Crystallography Printed in Great Britain - all rights reserved.",
author = "Mughal, {Robila K.} and Pritchard, {Robin G.} and Davey, {Roger J.}",
year = "2004",
month = "11",
doi = "10.1107/S1600536804025024",
language = "English",
volume = "60",
pages = "o1984--o1986",
journal = "Acta Crystallographica E: Crystallographic communications",
issn = "1600-5368",
publisher = "John Wiley & Sons Ltd",
number = "11",

}

RIS

TY - JOUR

T1 - (RS)-benzyl mandelate

AU - Mughal, Robila K.

AU - Pritchard, Robin G.

AU - Davey, Roger J.

PY - 2004/11

Y1 - 2004/11

N2 - A benzyl ester of mandelic acid, C15H14O 3, was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen-bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality. © 2004 International Union of Crystallography Printed in Great Britain - all rights reserved.

AB - A benzyl ester of mandelic acid, C15H14O 3, was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen-bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality. © 2004 International Union of Crystallography Printed in Great Britain - all rights reserved.

U2 - 10.1107/S1600536804025024

DO - 10.1107/S1600536804025024

M3 - Article

VL - 60

SP - o1984-o1986

JO - Acta Crystallographica E: Crystallographic communications

JF - Acta Crystallographica E: Crystallographic communications

SN - 1600-5368

IS - 11

ER -