Versatile synthesis of myo-inositol phospholipid precursors

Simon J. A. Grove; Ian H. Gilbert; Andrew B. Holmes; Gavin F. Painter; Malcolm L. Hill

doi:10.1039/A703044D

Versatile synthesis of myo-inositol phospholipid precursors

Simon J. A. Grove
, Ian H. Gilbert
, Andrew B. Holmes
, Gavin F. Painter
, Malcolm L. Hill

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

12 Citations (Scopus)

Abstract

Homochiral myo-inositol derivatives 16 and 20 and their corresponding enantiomers possessing either the natural or unnatural ring stereochemistry for inositol phospholipids are synthesised from myo-inositol derivatives 8 and 9 respectively using camphor dimethyl acetals in a resolution-protection sequence.

Original language	English
Pages (from-to)	1633-1634
Number of pages	2
Journal	Chemical Communications
Issue number	17
DOIs	https://doi.org/10.1039/A703044D
Publication status	Published - 1997

Access to Document

10.1039/A703044D

Cite this

@article{fb44c840868846718090a455e93c9441,

title = "Versatile synthesis of myo-inositol phospholipid precursors",

abstract = "Homochiral myo-inositol derivatives 16 and 20 and their corresponding enantiomers possessing either the natural or unnatural ring stereochemistry for inositol phospholipids are synthesised from myo-inositol derivatives 8 and 9 respectively using camphor dimethyl acetals in a resolution-protection sequence.",

author = "Grove, \{Simon J. A.\} and Gilbert, \{Ian H.\} and Holmes, \{Andrew B.\} and Painter, \{Gavin F.\} and Hill, \{Malcolm L.\}",

year = "1997",

doi = "10.1039/A703044D",

language = "English",

pages = "1633--1634",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "17",

}

TY - JOUR

T1 - Versatile synthesis of myo-inositol phospholipid precursors

AU - Grove, Simon J. A.

AU - Gilbert, Ian H.

AU - Holmes, Andrew B.

AU - Painter, Gavin F.

AU - Hill, Malcolm L.

PY - 1997

Y1 - 1997

N2 - Homochiral myo-inositol derivatives 16 and 20 and their corresponding enantiomers possessing either the natural or unnatural ring stereochemistry for inositol phospholipids are synthesised from myo-inositol derivatives 8 and 9 respectively using camphor dimethyl acetals in a resolution-protection sequence.

AB - Homochiral myo-inositol derivatives 16 and 20 and their corresponding enantiomers possessing either the natural or unnatural ring stereochemistry for inositol phospholipids are synthesised from myo-inositol derivatives 8 and 9 respectively using camphor dimethyl acetals in a resolution-protection sequence.

U2 - 10.1039/A703044D

DO - 10.1039/A703044D

M3 - Article

SN - 1359-7345

SP - 1633

EP - 1634

JO - Chemical Communications

JF - Chemical Communications

IS - 17

ER -

Versatile synthesis of myo-inositol phospholipid precursors

Abstract

Access to Document

Fingerprint

Cite this