Jaume Farràs, Ph.D.
Affiliations: | 1989- | Organic Chemistry | Universitat de Barcelona, Barcelona, Cataluña, Spain |
Area:
Synthetic methodologyWebsite:
http://www.qo.ub.edu/personals/jfarras/es/presentacio.htmlGoogle:
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Publications
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| Rodríguez A, Albert J, Ariza X, et al. (2014) Catalytic C-H activation of phenylethylamines or benzylamines and their annulation with allenes. The Journal of Organic Chemistry. 79: 9578-85 |
| Velasco J, Ariza X, Badía L, et al. (2013) Total Synthesis of Entecavir Journal of Organic Chemistry. 78: 5482-5491 |
| Sánchez C, Ariza X, Cornellà J, et al. (2010) Stereodivergent addition of 4-silyloxy-1,2-allenes to aldehydes by hydroboration. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 11535-8 |
| Terrazas M, Ariza X, Farràs J, et al. (2005) A novel nucleophilic approach to 1-alkyladenosines. A two-step synthesis of [1-15N]adenosine from inosine. Chemical Communications (Cambridge, England). 3968-70 |
| Pineda O, Farràs J, Maccari L, et al. (2005) Computational comparison of microtubule-stabilising agents laulimalide and peloruside with taxol and colchicine. Bioorganic & Medicinal Chemistry Letters. 14: 4825-9 |
| Terrazas M, Ariza X, Farràs J, et al. (2004) A direct, efficient method for the preparation of n6-protected 15n-labeled adenosines. The Journal of Organic Chemistry. 69: 5473-5 |
| Ariza X, Bach J, Berenguer R, et al. (2004) Highly stereoselective approach to alk-2-yne-1,4-diols by oxazaborolidine-mediated reduction of alk-2-yne-1,4-diones. Journal of Organic Chemistry. 69: 5307-5313 |