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Journal article

A synthesis of dioctanoyl phosphatidylinositol

Abstract:: A synthesis of the naturally occurring enantiomer of phosphatidylinositol is reported. A resolution strategy, using camphor as a chiral auxiliary is employed to obtain the desired, enantiomerically pure, inositol derivative. Dioctanoyl lipid chains are appended to the molecule, which are shorter than the naturally occurring lipid chains, providing the molecule with enhanced water solubility. © 2009 Elsevier Ltd. All rights reserved.

Publication status:: Published

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APA Style

Elliott, T., Nemeth, J., Swain, S. A., & Conway, S. (2009). A synthesis of dioctanoyl phosphatidylinositol. TETRAHEDRON-ASYMMETRY, 20(24), 2809–2813.

MLA Style

Elliott, T., et al. “A Synthesis of Dioctanoyl Phosphatidylinositol.” TETRAHEDRON-ASYMMETRY, vol. 20, no. 24, 2009, pp. 2809–13.

Chicago Style

Elliott, T, J Nemeth, SA Swain, and S Conway. 2009. “A Synthesis of Dioctanoyl Phosphatidylinositol.” TETRAHEDRON-ASYMMETRY 20 (24): 2809–13.
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Publisher copy:: 10.1016/j.tetasy.2009.11.026

Authors

+ Elliott, T More by this author

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Author

+ Nemeth, J More by this author

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Author

+ Swain, SA More by this author

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Author

+ Conway, S More by this author

Institution:

University of Oxford

Division:

MPLS

Department:

Chemistry

Sub department:

Organic Chemistry

Role:

Author

Bibliographic Details

Journal:: TETRAHEDRON-ASYMMETRY
Volume:: 20
Issue:: 24
Pages:: 2809-2813
Publication date:: 2009-12-22
DOI:: 10.1016/j.tetasy.2009.11.026
EISSN:: 1362-511X
ISSN:: 0957-4166

Item Description

Language:: English
Pubs id:: pubs:50325
UUID:: uuid:03f6315a-16d4-4a1e-9d2b-422eb5648ee0
Local pid:: pubs:50325
Source identifiers:: 50325
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2009

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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