Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate gives rapid access to precursors for second messenger analogues

Andrew M. Riley; H. Yasmin Godage; Mary F. Mahon; Barry V. L. Potter

doi:10.1016/j.tetasy.2005.12.008

Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate gives rapid access to precursors for second messenger analogues

Andrew M. Riley, H. Yasmin Godage, Mary F. Mahon, Barry V. L. Potter

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

22 Citations (SciVal)

Abstract

Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate via the formation of diastereoisomeric bis[(1S)-(-)-camphanate] esters provides a convenient and fast route to precursors for biologically important inositol phosphates and lipids, and to synthetic analogues and probes modified at O-1 or O-3 of the inositol ring.

Original language	English
Pages (from-to)	171-174
Number of pages	4
Journal	Tetrahedron: Asymmetry
Volume	17
Issue number	2
DOIs	https://doi.org/10.1016/j.tetasy.2005.12.008
Publication status	Published - 2006

Access to Document

10.1016/j.tetasy.2005.12.008

Cite this

@article{0c8856459eab4bacb9ddfc08c98e3bc9,

title = "Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate gives rapid access to precursors for second messenger analogues",

abstract = "Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate via the formation of diastereoisomeric bis[(1S)-(-)-camphanate] esters provides a convenient and fast route to precursors for biologically important inositol phosphates and lipids, and to synthetic analogues and probes modified at O-1 or O-3 of the inositol ring.",

author = "Riley, \{Andrew M.\} and Godage, \{H. Yasmin\} and Mahon, \{Mary F.\} and Potter, \{Barry V. L.\}",

year = "2006",

doi = "10.1016/j.tetasy.2005.12.008",

language = "English",

volume = "17",

pages = "171--174",

journal = "Tetrahedron: Asymmetry",

issn = "0957-4166",

publisher = "Elsevier",

number = "2",

}

TY - JOUR

T1 - Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate gives rapid access to precursors for second messenger analogues

AU - Riley, Andrew M.

AU - Godage, H. Yasmin

AU - Mahon, Mary F.

AU - Potter, Barry V. L.

PY - 2006

Y1 - 2006

N2 - Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate via the formation of diastereoisomeric bis[(1S)-(-)-camphanate] esters provides a convenient and fast route to precursors for biologically important inositol phosphates and lipids, and to synthetic analogues and probes modified at O-1 or O-3 of the inositol ring.

AB - Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate via the formation of diastereoisomeric bis[(1S)-(-)-camphanate] esters provides a convenient and fast route to precursors for biologically important inositol phosphates and lipids, and to synthetic analogues and probes modified at O-1 or O-3 of the inositol ring.

UR - http://dx.doi.org/10.1016/j.tetasy.2005.12.008

UR - https://www.scopus.com/pages/publications/32444445836

U2 - 10.1016/j.tetasy.2005.12.008

DO - 10.1016/j.tetasy.2005.12.008

M3 - Article

SN - 0957-4166

VL - 17

SP - 171

EP - 174

JO - Tetrahedron: Asymmetry

JF - Tetrahedron: Asymmetry

IS - 2

ER -

Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate gives rapid access to precursors for second messenger analogues

Abstract

Access to Document

Other files and links

Fingerprint

Cite this