1 | Gold-Catalyzed Partial Hydrogenation of Activated Alkynes Mediated by Triphenylphosphine | Coautor: Maricela Mastranzo, Virginia, Patricia Cocoletzi-Xochitiotzi, Ana, Hernandez-Hernandez, Miguel, Medina-Mercado, Ignacio, et al. | 2020 | Synthesis-Stuttgart | WoS-id: 000554994000010 Scopus-id: 2-s2.0-85089361247
| 3 | 3 |
2 | Cerebrolysin reduces mechanical allodynia in a rodent model of peripheral inflammation | Coautor: Mastranzo, V.M., Morales-Medina, J.C., Griffiths, N.H., Flores, G., et al. | 2017 | NEUROSCIENCE LETTERS | WoS-id: 000397356300005 Scopus-id: 2-s2.0-85011349868
| 10 | 10 |
3 | Chiron approach to formal synthesis of 8,9-dideoxyneodysiherbaine (MSVIII-19) | 2ᵒ autor: Mastranzo, V.M., Sanchez-Eleuterio, A., Quintero, L., Sartillo-Piscil, F. | 2017 | LETTERS IN ORGANIC CHEMISTRY | WoS-id: 000403644000007 Scopus-id: 2-s2.0-85022191998
| 3 | 3 |
4 | Synthesis of 5-hydroxy hydantoins via a tandem process | Coautor: Mastranzo, V.M., Meza-León, R.L., Bernès, S., Cortés-López, G.N., et al. | 2016 | TETRAHEDRON LETTERS | WoS-id: 000382419200028 Scopus-id: 2-s2.0-84983050292
| 5 | 4 |
5 | Erratum: Short stereoselective synthesis of (+)-crispine A via an N-sulfinyl Pictet-Spengler reaction (Tetrahedron Letters (2013) 54 (1893-1896)) | Coautor: Mastranzo V.M., Sánchez-Obregón R., Ortiz B., Yuste F., et al. | 2014 | TETRAHEDRON LETTERS | WoS-id: 000340339000022 Scopus-id: 2-s2.0-84940294221
| 0 | 0 |
6 | Short stereoselective synthesis of (+)-crispine A via an N-sulfinyl Pictet-Spengler reaction | Coautor: Mastranzo V.M., Sánchez-Obregón R., Ortiz B., Yuste F., et al. | 2013 | TETRAHEDRON LETTERS | WoS-id: 000316095000028 Scopus-id: 2-s2.0-84875213956
| 16 | 17 |
7 | Asymmetric synthesis of (S)-(-)-tetrahydropalmatine and (S)-(-)-canadine via a sulfinyl-directed Pictet-Spengler cyclization | 1ᵉʳ autor: Mastranzo V.M., Romero, JLO, Yuste F., Ortiz B., et al. | 2012 | Tetrahedron | WoS-id: 000300028800040 Scopus-id: 2-s2.0-84855431364
| 15 | 16 |
8 | One-pot synthesis of sulfonamides from methyl sulfinates using ultrasound | Coautor: Mastranzo, VM, Ruano, JLG, Parra, A, Marzo, L, et al. | 2011 | Tetrahedron | WoS-id: 000289862700013 Scopus-id: 2-s2.0-79953171842
| 40 | 38 |
9 | Methyl Sulfinates as Electrophiles in Friedel-Crafts Reactions. Synthesis of Aryl Sulfoxides | Coautor: Mastranzo, VM, Yuste, F, Linares, AH, Ortiz, B, et al. | 2011 | JOURNAL OF ORGANIC CHEMISTRY | WoS-id: 000291128300031 Scopus-id: 2-s2.0-79957858784
| 54 | 57 |
10 | Asymmetric Synthesis of (S)-(-)-Xylopinine. Use of the Sulfinyl Group as an Ipso Director in Aromatic S-E | 1ᵉʳ autor: Mastranzo V.M., Yuste F., Ortiz B., Sánchez-Obregón R., et al. | 2011 | JOURNAL OF ORGANIC CHEMISTRY | WoS-id: 000291409900023 Scopus-id: 2-s2.0-79958785731
| 33 | 39 |
11 | 1,2-Dimethoxy-4-methyl-3-[(S)-p-tolylsulfinyl]benzene | 1ᵉʳ autor: Mastranzo, VM, Olivares, JL, Sanchez-Obregon, R, Yuste, F, et al. | 2011 | ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE | WoS-id: 000297859000047 Scopus-id: 2-s2.0-84455210153
| 1 | 1 |
12 | Monoalkylation of primary amines and N-sulfinylamides | Coautor: Mastranzo V.M., Ruano, JLG, Parra A., Alemán J., et al. | 2009 | CHEMICAL COMMUNICATIONS | WoS-id: 000262398500004 Scopus-id: 2-s2.0-58149458879
| 42 | 38 |
13 | Catalytic asymmetric hydrosilylation of acetophenone with new chiral thiourea ligands containing the (S)-alpha-phenylethyl group | Coautor: Mastranzo V.M., Santacruz E., Huelgas G., Angulo S.K., et al. | 2009 | TETRAHEDRON-ASYMMETRY | WoS-id: 000274985000004 Scopus-id: 2-s2.0-74349113365
| 19 | 24 |
14 | A formal synthesis of (+)-(S)-kurasoin B | 2ᵒ autor: Mastranzo V.M., Yuste F., Sánchez-Obregón R., Ortiz B., et al. | 2009 | Arkivoc | Scopus-id: 2-s2.0-77951874401
| 0 | 2 |
15 | Mild and general method for the synthesis of sulfonamides | Coautor: Mastranzo V.M., Ruano, JLG, Parra A., Yuste F. | 2008 | Synthesis-Stuttgart | WoS-id: 000252846900020 Scopus-id: 2-s2.0-38849091996
| 58 | 35 |
16 | Determination of the enantiomeric excess of chiral carboxylic acids by 31P NMR with phosphorylated derivatizing agents from C 2-symmetrical diamines containing the (S)-a-phenylethyl group | 1ᵉʳ autor: Mastranzo V.M., Quintero L., De Parrodi C.A. | 2007 | Chirality | WoS-id: 000247128300011 Scopus-id: 2-s2.0-34250214123
| 8 | 7 |
17 | Synthesis of chiral ligands containing the N-(S)-a-phenylethyl group and their evaluation as activators in the enantioselective addition of Et2Zn to benzaldehyde | 1ᵉʳ autor: Mastranzo V.M., Santacruz E., Huelgas G., Paz E., et al. | 2006 | TETRAHEDRON-ASYMMETRY | WoS-id: 000239522700010 Scopus-id: 2-s2.0-33745809479
| 14 | 17 |
18 | Use of diamines containing the a-phenylethyl group as chiral ligands in the asymmetric hydrosilylation of prochiral ketones | 1ᵉʳ autor: Mastranzo V.M., Quintero L., De Parrodi C.A., Juaristi E., et al. | 2004 | Tetrahedron | WoS-id: 000188944400007 Scopus-id: 2-s2.0-0842310704
| 82 | 87 |