A Potential Route to Neuroprostanes and Isoprostanes: Preparation of the Four Enantiomerically Pure Diastereomers of 13-F4t-NeuroP-Reference-Cited by-同舟云学术

A Potential Route to Neuroprostanes and Isoprostanes: Preparation of the Four Enantiomerically Pure Diastereomers of 13-F4t-NeuroP

Published:2008-03-15 Issue:9 Volume:73 Page:3467-3474
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Taber Douglass F.¹,Reddy P. Ganapati¹,Arneson Kyle O.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, and Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo702600v

Reference60 articles.

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4. Formation of Novel D-Ring and E-Ring Isoprostane-like Compounds (D4/E4-Neuroprostanes) in Vivo from Docosahexaenoic Acid

5. The biochemistry of the isoprostane, neuroprostane, and isofuran pathways of lipid peroxidation

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