Generating rapamycin analogues by directed biosynthesis: starter acid substrate specificity of mono-substituted cyclohexane carboxylic acids

Rebecca J. M. Goss; Simon E. Lanceron; Nicola J. Wise; Steven J. Moss

doi:10.1039/b614519c

Generating rapamycin analogues by directed biosynthesis: starter acid substrate specificity of mono-substituted cyclohexane carboxylic acids

Rebecca J. M. Goss^*, Simon E. Lanceron, Nicola J. Wise, Steven J. Moss

^*Corresponding author for this work

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

Abstract

We report a convenient synthesis of 4-fluorocyclohexanoic acid, and an insight into the rules governing acceptance of starter acid analogues in the precursor-directed biosynthesis of rapamycin.

Original language	English
Pages (from-to)	4071-4073
Number of pages	3
Journal	Organic & Biomolecular Chemistry
Volume	4
Issue number	22
DOIs	https://doi.org/10.1039/b614519c
Publication status	Published - 2006

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10.1039/b614519c

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title = "Generating rapamycin analogues by directed biosynthesis: starter acid substrate specificity of mono-substituted cyclohexane carboxylic acids",

abstract = "We report a convenient synthesis of 4-fluorocyclohexanoic acid, and an insight into the rules governing acceptance of starter acid analogues in the precursor-directed biosynthesis of rapamycin.",

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author = "Goss, \{Rebecca J. M.\} and Lanceron, \{Simon E.\} and Wise, \{Nicola J.\} and Moss, \{Steven J.\}",

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AU - Goss, Rebecca J. M.

AU - Lanceron, Simon E.

AU - Wise, Nicola J.

AU - Moss, Steven J.

PY - 2006

Y1 - 2006

N2 - We report a convenient synthesis of 4-fluorocyclohexanoic acid, and an insight into the rules governing acceptance of starter acid analogues in the precursor-directed biosynthesis of rapamycin.

AB - We report a convenient synthesis of 4-fluorocyclohexanoic acid, and an insight into the rules governing acceptance of starter acid analogues in the precursor-directed biosynthesis of rapamycin.

KW - UNIT

UR - https://www.scopus.com/pages/publications/33750505007

U2 - 10.1039/b614519c

DO - 10.1039/b614519c

M3 - Article

SN - 1477-0520

VL - 4

SP - 4071

EP - 4073

JO - Organic & Biomolecular Chemistry

JF - Organic & Biomolecular Chemistry

IS - 22

ER -

Generating rapamycin analogues by directed biosynthesis: starter acid substrate specificity of mono-substituted cyclohexane carboxylic acids

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