(2R,3S,4S,5R)-4-hydroxy-3-iodo-5-methyltetrahydro-2-furylmethyl benzoate

S. P. Bew; M. E. Light; M. B. Hursthouse; D. W. Knight; R. J. Middleton

doi:10.1107/s1600536800018614

(2R,3S,4S,5R)-4-hydroxy-3-iodo-5-methyltetrahydro-2-furylmethyl benzoate

S. P. Bew, M. E. Light, M. B. Hursthouse, D. W. Knight, R. J. Middleton

Chemistry of Materials and Catalysis

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

Abstract

The crystal structure determination of the title compound, C13H15IO4, has allowed the relative stereochemistry between the tetrasubstituted C atoms on the tetrahydrofuran moiety to be confirmed. The title compound is a precursor of the ionophoric antibiotic Aplasmomycin. The compound is involved in both intra- and intermolecular hydrogen bonding, the latter link the molecules into chains running along the b axis.

Original language	English
Pages (from-to)	O58-O60
Number of pages	3
Journal	Acta Crystallographica Section E
Volume	57
DOIs	https://doi.org/10.1107/s1600536800018614
Publication status	Published - 2001

Access to Document

10.1107/s1600536800018614

Cite this

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title = "(2R,3S,4S,5R)-4-hydroxy-3-iodo-5-methyltetrahydro-2-furylmethyl benzoate",

abstract = "The crystal structure determination of the title compound, C13H15IO4, has allowed the relative stereochemistry between the tetrasubstituted C atoms on the tetrahydrofuran moiety to be confirmed. The title compound is a precursor of the ionophoric antibiotic Aplasmomycin. The compound is involved in both intra- and intermolecular hydrogen bonding, the latter link the molecules into chains running along the b axis.",

author = "Bew, {S. P.} and Light, {M. E.} and Hursthouse, {M. B.} and Knight, {D. W.} and Middleton, {R. J.}",

year = "2001",

doi = "10.1107/s1600536800018614",

language = "English",

volume = "57",

pages = "O58--O60",

journal = "Acta Crystallographica Section E",

}

TY - JOUR

T1 - (2R,3S,4S,5R)-4-hydroxy-3-iodo-5-methyltetrahydro-2-furylmethyl benzoate

AU - Bew, S. P.

AU - Light, M. E.

AU - Hursthouse, M. B.

AU - Knight, D. W.

AU - Middleton, R. J.

PY - 2001

Y1 - 2001

N2 - The crystal structure determination of the title compound, C13H15IO4, has allowed the relative stereochemistry between the tetrasubstituted C atoms on the tetrahydrofuran moiety to be confirmed. The title compound is a precursor of the ionophoric antibiotic Aplasmomycin. The compound is involved in both intra- and intermolecular hydrogen bonding, the latter link the molecules into chains running along the b axis.

AB - The crystal structure determination of the title compound, C13H15IO4, has allowed the relative stereochemistry between the tetrasubstituted C atoms on the tetrahydrofuran moiety to be confirmed. The title compound is a precursor of the ionophoric antibiotic Aplasmomycin. The compound is involved in both intra- and intermolecular hydrogen bonding, the latter link the molecules into chains running along the b axis.

U2 - 10.1107/s1600536800018614

DO - 10.1107/s1600536800018614

M3 - Article

VL - 57

SP - O58-O60

JO - Acta Crystallographica Section E

JF - Acta Crystallographica Section E

ER -