Porta A - Search Results

1

A general enantioselective approach to jasmonoid fragrances: synthesis of (+)-(1R,2S)-methyl dihydrojasmonate and (+)-(1R,2S)-magnolione.

Porta A, Vidari G, Zanoni G. Porta A, et al. J Org Chem. 2005 Jun 10;70(12):4876-8. doi: 10.1021/jo050423p. J Org Chem. 2005. PMID: 15932335

2

First total synthesis of A(2) isoprostane.

Zanoni G, Porta A, Vidari G. Zanoni G, et al. Among authors: porta a. J Org Chem. 2002 Jun 14;67(12):4346-51. doi: 10.1021/jo025652f. J Org Chem. 2002. PMID: 12054973

3

1,2-Oxopalladation versus pi-allyl palladium route. A regioconvergent approach to a key intermediate for cyclopentanoids synthesis. New insights into the Pd(II)-catalyzed lactonization reaction.

Zanoni G, Porta A, Meriggi A, Franzini M, Vidari G. Zanoni G, et al. Among authors: porta a. J Org Chem. 2002 Aug 23;67(17):6064-9. doi: 10.1021/jo025722i. J Org Chem. 2002. PMID: 12182643

4

First total synthesis of JS isoprostane.

Zanoni G, Porta A, Castronovo F, Vidari G. Zanoni G, et al. Among authors: porta a. J Org Chem. 2003 Jul 25;68(15):6005-10. doi: 10.1021/jo034658h. J Org Chem. 2003. PMID: 12868940

5

First enantioselective total synthesis of (8S,12R,15S)-prostaglandin J(2).

Zanoni G, Porta A, De Toma Q, Castronovo F, Vidari G. Zanoni G, et al. Among authors: porta a. J Org Chem. 2003 Aug 8;68(16):6437-9. doi: 10.1021/jo034502h. J Org Chem. 2003. PMID: 12895084

6

The cyclopentenone product of lipid peroxidation, 15-A2t-isoprostane, is efficiently metabolized by HepG2 cells via conjugation with glutathione.

Milne GL, Zanoni G, Porta A, Sasi S, Vidari G, Musiek ES, Freeman ML, Morrow JD. Milne GL, et al. Among authors: porta a. Chem Res Toxicol. 2004 Jan;17(1):17-25. doi: 10.1021/tx034213o. Chem Res Toxicol. 2004. PMID: 14727915

7

Identification of the major urinary metabolite of the highly reactive cyclopentenone isoprostane 15-A(2t)-isoprostane in vivo.

Milne GL, Gao L, Porta A, Zanoni G, Vidari G, Morrow JD. Milne GL, et al. Among authors: porta a. J Biol Chem. 2005 Jul 1;280(26):25178-84. doi: 10.1074/jbc.M502891200. Epub 2005 May 5. J Biol Chem. 2005. PMID: 15878849 Free article.

8

Asymmetric synthesis of a chiral building block for cyclopentanoids: a novel enantioselective synthesis of preclavulone A.

Zanoni G, Porta A, Brunoldi E, Vidari G. Zanoni G, et al. Among authors: porta a. J Org Chem. 2006 Oct 27;71(22):8459-66. doi: 10.1021/jo061321h. J Org Chem. 2006. PMID: 17064020

9

Asymmetric synthesis of 14-A4t-neuroprostane: hunting for a suitable biomarker for neurodegenerative diseases.

Zanoni G, Brunoldi EM, Porta A, Vidari G. Zanoni G, et al. Among authors: porta a. J Org Chem. 2007 Dec 7;72(25):9698-703. doi: 10.1021/jo701719f. Epub 2007 Nov 10. J Org Chem. 2007. PMID: 17994761

10

Electrophilic cyclopentenone neuroprostanes are anti-inflammatory mediators formed from the peroxidation of the omega-3 polyunsaturated fatty acid docosahexaenoic acid.

Musiek ES, Brooks JD, Joo M, Brunoldi E, Porta A, Zanoni G, Vidari G, Blackwell TS, Montine TJ, Milne GL, McLaughlin B, Morrow JD. Musiek ES, et al. Among authors: porta a. J Biol Chem. 2008 Jul 18;283(29):19927-35. doi: 10.1074/jbc.M803625200. Epub 2008 May 19. J Biol Chem. 2008. PMID: 18490445 Free PMC article.

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