An Efficient Preparation of Isosteric Phosphonate Analogues of Sphingolipids by Opening of Oxirane and Cyclic Sulfamidate Intermediates with α-Lithiated Alkylphosphonic Esters-Reference-Cited by-同舟云学术

An Efficient Preparation of Isosteric Phosphonate Analogues of Sphingolipids by Opening of Oxirane and Cyclic Sulfamidate Intermediates with α-Lithiated Alkylphosphonic Esters

Published:2004-10-01 Issue:22 Volume:69 Page:7694-7699
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sun Chaode¹,Bittman Robert¹

Affiliation:

1. Department of Chemistry and Biochemistry, Queens College of The City University of New York, Flushing, New York 11367-1597

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0487404

Reference31 articles.

1. (b) Merrill, A. H., Jr.; Sandhoff, K. InBiochemistry of Lipids,Lipoproteins, and Membranes, 4th ed.; Vance, D. E., Vance, J. E., Eds.; Elsevier: Amsterdam, 2002; pp 373−407.

2. Functional characterization of sphingolipid C4-hydroxylase genes fromArabidopsis thaliana

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