Rossi JC - Search Results

1

Quantification of urinary F2-isoprostanes with 4(RS)-F4t-neuroprostane as an internal standard using gas chromatography-mass spectrometry Application to polytraumatized patients.

Mas E, Michel F, Guy A, Bultel V, Falquet Y, Chardon P, Rossi JC, Cristol JP, Durand T. Mas E, et al. Among authors: rossi jc. J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Sep 1;872(1-2):133-40. doi: 10.1016/j.jchromb.2008.07.037. Epub 2008 Aug 3. J Chromatogr B Analyt Technol Biomed Life Sci. 2008. PMID: 18706873

2

Total synthesis of (15R)- and (15S)-F(2t)-isoprostanes by a biomimetic process using the cyclization of acyclic dihydroxylated octa-5,7-dienyl radicals.

Durand T, Guy A, Vidal JP, Rossi JC. Durand T, et al. Among authors: rossi jc. J Org Chem. 2002 May 31;67(11):3615-24. doi: 10.1021/jo0109624. J Org Chem. 2002. PMID: 12027672

3

Tandem mass spectrometric quantification of 8-iso-prostaglandin F2alpha and its metabolite 2,3-dinor-5,6-dihydro-8-iso-prostaglandin F2alpha in human urine.

Schwedhelm E, Tsikas D, Durand T, Gutzki FM, Guy A, Rossi JC, Frölich JC. Schwedhelm E, et al. Among authors: rossi jc. J Chromatogr B Biomed Sci Appl. 2000 Jul 7;744(1):99-112. doi: 10.1016/s0378-4347(00)00236-x. J Chromatogr B Biomed Sci Appl. 2000. PMID: 10985571

4

The 5-series F(2)-isoprostanes possess no vasomotor effects in the rat thoracic aorta, the human internal mammary artery and the human saphenous vein.

Marlière S, Cracowski JL, Durand T, Chavanon O, Bessard J, Guy A, Stanke-Labesque F, Rossi JC, Bessard G. Marlière S, et al. Among authors: rossi jc. Br J Pharmacol. 2002 Mar;135(5):1276-80. doi: 10.1038/sj.bjp.0704558. Br J Pharmacol. 2002. PMID: 11877336 Free PMC article.

5

Identification of metabolites from type III F2-isoprostane diastereoisomers by mass spectrometry.

Chiabrando C, Rivalta C, Bagnati R, Valagussa A, Durand T, Guy A, Villa P, Rossi JC, Fanelli R. Chiabrando C, et al. Among authors: rossi jc. J Lipid Res. 2002 Mar;43(3):495-509. J Lipid Res. 2002. PMID: 11893786 Free article.

6

Total synthesis of the eight diastereomers of the syn-anti-syn phytoprostanes F1 types I and II.

El Fangour S, Guy A, Despres V, Vidal JP, Rossi JC, Durand T. El Fangour S, et al. Among authors: rossi jc. J Org Chem. 2004 Apr 2;69(7):2498-503. doi: 10.1021/jo035638i. J Org Chem. 2004. PMID: 15049650

7

Total Synthesis of the Four Enantiomerically Pure Diasteroisomers of the Phytoprostanes E1Type II and of the 15-E2t-Isoprostanes.

Pinot E, Guy A, Fournial A, Balas L, Rossi JC, Durand T. Pinot E, et al. Among authors: rossi jc. J Org Chem. 2008 Apr 18;73(8):3063-9. doi: 10.1021/jo702455g. Epub 2008 Mar 20. J Org Chem. 2008. PMID: 18351775

8

The handy use of Brown's P2-Ni catalyst for a skipped diyne deuteration: application to the synthesis of a [D4]-labeled F4t-neuroprostane.

Oger C, Bultel-Poncé V, Guy A, Balas L, Rossi JC, Durand T, Galano JM. Oger C, et al. Among authors: rossi jc. Chemistry. 2010 Dec 17;16(47):13976-80. doi: 10.1002/chem.201002304. Chemistry. 2010. PMID: 21077063 No abstract available.

9

Total syntheses of iso-, neuro- and phytoprostanes: new insight in lipid chemistry.

Durand T, Guy A, Henry O, Roland A, Bernad S, El Fangour S, Vidal JP, Rossi JC. Durand T, et al. Among authors: rossi jc. Chem Phys Lipids. 2004 Mar;128(1-2):15-33. doi: 10.1016/j.chemphyslip.2003.10.008. Chem Phys Lipids. 2004. PMID: 15037150 Review.

10

A flexible synthesis of the phytoprostanes B1 type I and II.

El Fangour S, Guy A, Vidal JP, Rossi JC, Durand T. El Fangour S, et al. Among authors: rossi jc. J Org Chem. 2005 Feb 4;70(3):989-97. doi: 10.1021/jo048179+. J Org Chem. 2005. PMID: 15675859

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