"Inosaminoacids": novel inositol-amino acid hybrid structures accessed by microbial arene oxidation

S Pilgrim; Gabriele Kociok-Kohn; Matthew D Lloyd; Simon E Lewis

doi:10.1039/c1cc10643k

"Inosaminoacids": novel inositol-amino acid hybrid structures accessed by microbial arene oxidation

S Pilgrim, Gabriele Kociok-Kohn, Matthew D Lloyd, Simon E Lewis

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Abstract

Microbial 1,2-dihydroxylation of sodium benzoate permits the rapid construction of novel inositol-amino acid hybrid structures. Both beta- and gamma-amino acids are accessible by means of an acylnitroso Diels-Alder cycloaddition.

Original language	English
Pages (from-to)	4799-4801
Number of pages	3
Journal	Chemical Communications
Volume	47
Issue number	16
Early online date	15 Mar 2011
DOIs	https://doi.org/10.1039/c1cc10643k
Publication status	Published - 28 Apr 2011

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title = "{"}Inosaminoacids{"}: novel inositol-amino acid hybrid structures accessed by microbial arene oxidation",

abstract = "Microbial 1,2-dihydroxylation of sodium benzoate permits the rapid construction of novel inositol-amino acid hybrid structures. Both beta- and gamma-amino acids are accessible by means of an acylnitroso Diels-Alder cycloaddition.",

author = "S Pilgrim and Gabriele Kociok-Kohn and Lloyd, \{Matthew D\} and Lewis, \{Simon E\}",

year = "2011",

month = apr,

day = "28",

doi = "10.1039/c1cc10643k",

language = "English",

volume = "47",

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publisher = "Royal Society of Chemistry",

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T1 - "Inosaminoacids": novel inositol-amino acid hybrid structures accessed by microbial arene oxidation

AU - Pilgrim, S

AU - Kociok-Kohn, Gabriele

AU - Lloyd, Matthew D

AU - Lewis, Simon E

PY - 2011/4/28

Y1 - 2011/4/28

N2 - Microbial 1,2-dihydroxylation of sodium benzoate permits the rapid construction of novel inositol-amino acid hybrid structures. Both beta- and gamma-amino acids are accessible by means of an acylnitroso Diels-Alder cycloaddition.

AB - Microbial 1,2-dihydroxylation of sodium benzoate permits the rapid construction of novel inositol-amino acid hybrid structures. Both beta- and gamma-amino acids are accessible by means of an acylnitroso Diels-Alder cycloaddition.

UR - https://www.scopus.com/pages/publications/79953701655

UR - http://dx.doi.org/10.1039/c1cc10643k

U2 - 10.1039/c1cc10643k

DO - 10.1039/c1cc10643k

M3 - Article

SN - 1359-7345

VL - 47

SP - 4799

EP - 4801

JO - Chemical Communications

JF - Chemical Communications

IS - 16

ER -

"Inosaminoacids": novel inositol-amino acid hybrid structures accessed by microbial arene oxidation

Abstract

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