VIRGINIA MARICELA MASTRANZO CORONA



DATOS GENERALES NOMBRAMIENTOS
Nombre completo   VIRGINIA MARICELA MASTRANZO CORONA
Máximo nivel de estudios   DOCTORADO
Antigüedad académica en la UNAM   7 años, 9 meses, 16 días

Último  INVESTIGADOR ASOCIADO C TC No Definitivo
Instituto de Química
ESTIMULOS, PROGRAMAS, PREMIOS Y RECONOCIMIENTOS
* SNI I2011 - 2017
* SNI C2009 - 2010

INFORMACIÓN DE PUBLICACIONES
Firmas  
Maricela Mastranzo, Virginia Mastranzo V.M. Mastranzo, V.M. Mastranzo, VM
ID's SCOPUS  
6507560621 56000896200
Áreas de conocimiento  
Crystallography Chemistry, inorganic & nuclear Chemistry, multidisciplinary Chemistry, organic Chemistry, physical
Jcs 2008 Neurosciences Scie jcr Biochemistry Drug Discovery
Inorganic Chemistry Materials Chemistry Materials Science (miscellaneous) Neuroscience (miscellaneous) Organic Chemistry
Coautorías con entidades de la UNAM  
  • Instituto de Química
  • Facultad de Química
Revistas en las que ha publicado  (11):
  1. ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, Dinamarca (2011)
  2. Arkivoc, (2009)
  3. CHEMICAL COMMUNICATIONS, Reino Unido (2009)
  4. Chirality, Estados Unidos America (2007)
  5. JOURNAL OF ORGANIC CHEMISTRY, Estados Unidos America (2011)
  6. LETTERS IN ORGANIC CHEMISTRY, (2017)
  7. NEUROSCIENCE LETTERS, Irlanda (2017)
  8. Synthesis-Stuttgart, Alemania (2008, 2020)
  9. Tetrahedron, Reino Unido (2004, 2011, 2012)
  10. TETRAHEDRON LETTERS, Reino Unido (2013, 2014, 2016)
  11. TETRAHEDRON-ASYMMETRY, Reino Unido (2006, 2009)


Documentos indexados (WoS y Scopus)

# Título del documento Autores Año Rista Fuente Citas WoS Citas Scopus
1Gold-Catalyzed Partial Hydrogenation of Activated Alkynes Mediated by TriphenylphosphineCoautor: Maricela Mastranzo, Virginia, Patricia Cocoletzi-Xochitiotzi, Ana, Hernandez-Hernandez, Miguel, Medina-Mercado, Ignacio, et al.2020Synthesis-StuttgartWoS-id: 000554994000010
Scopus-id: 2-s2.0-85089361247
22
2Cerebrolysin reduces mechanical allodynia in a rodent model of peripheral inflammationCoautor: Mastranzo, V.M., Morales-Medina, J.C., Griffiths, N.H., Flores, G., et al.2017NEUROSCIENCE LETTERSWoS-id: 000397356300005
Scopus-id: 2-s2.0-85011349868
810
3Chiron approach to formal synthesis of 8,9-dideoxyneodysiherbaine (MSVIII-19)2ᵒ autor: Mastranzo, V.M., Sanchez-Eleuterio, A., Quintero, L., Sartillo-Piscil, F.2017LETTERS IN ORGANIC CHEMISTRYWoS-id: 000403644000007
Scopus-id: 2-s2.0-85022191998
33
4Synthesis of 5-hydroxy hydantoins via a tandem processCoautor: Mastranzo, V.M., Meza-León, R.L., Bernès, S., Cortés-López, G.N., et al.2016TETRAHEDRON LETTERSWoS-id: 000382419200028
Scopus-id: 2-s2.0-84983050292
44
5Erratum: 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.2014TETRAHEDRON LETTERSWoS-id: 000340339000022
Scopus-id: 2-s2.0-84940294221
00
6Short stereoselective synthesis of (+)-crispine A via an N-sulfinyl Pictet-Spengler reactionCoautor: Mastranzo V.M., Sánchez-Obregón R., Ortiz B., Yuste F., et al.2013TETRAHEDRON LETTERSWoS-id: 000316095000028
Scopus-id: 2-s2.0-84875213956
1516
7Asymmetric synthesis of (S)-(-)-tetrahydropalmatine and (S)-(-)-canadine via a sulfinyl-directed Pictet-Spengler cyclization1ᵉʳ autor: Mastranzo V.M., Romero, JLO, Yuste F., Ortiz B., et al.2012TetrahedronWoS-id: 000300028800040
Scopus-id: 2-s2.0-84855431364
1316
8One-pot synthesis of sulfonamides from methyl sulfinates using ultrasoundCoautor: Mastranzo, VM, Ruano, JLG, Parra, A, Marzo, L, et al.2011TetrahedronWoS-id: 000289862700013
Scopus-id: 2-s2.0-79953171842
3837
9Methyl Sulfinates as Electrophiles in Friedel-Crafts Reactions. Synthesis of Aryl SulfoxidesCoautor: Mastranzo, VM, Yuste, F, Linares, AH, Ortiz, B, et al.2011JOURNAL OF ORGANIC CHEMISTRYWoS-id: 000291128300031
Scopus-id: 2-s2.0-79957858784
5154
10Asymmetric Synthesis of (S)-(-)-Xylopinine. Use of the Sulfinyl Group as an Ipso Director in Aromatic S-E1ᵉʳ autor: Mastranzo V.M., Yuste F., Ortiz B., Sánchez-Obregón R., et al.2011JOURNAL OF ORGANIC CHEMISTRYWoS-id: 000291409900023
Scopus-id: 2-s2.0-79958785731
2839
111,2-Dimethoxy-4-methyl-3-[(S)-p-tolylsulfinyl]benzene1ᵉʳ autor: Mastranzo, VM, Olivares, JL, Sanchez-Obregon, R, Yuste, F, et al.2011ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINEWoS-id: 000297859000047
Scopus-id: 2-s2.0-84455210153
11
12Monoalkylation of primary amines and N-sulfinylamidesCoautor: Mastranzo V.M., Ruano, JLG, Parra A., Alemán J., et al.2009CHEMICAL COMMUNICATIONSWoS-id: 000262398500004
Scopus-id: 2-s2.0-58149458879
3938
13Catalytic asymmetric hydrosilylation of acetophenone with new chiral thiourea ligands containing the (S)-alpha-phenylethyl groupCoautor: Mastranzo V.M., Santacruz E., Huelgas G., Angulo S.K., et al.2009TETRAHEDRON-ASYMMETRYWoS-id: 000274985000004
Scopus-id: 2-s2.0-74349113365
1722
14A formal synthesis of (+)-(S)-kurasoin B2ᵒ autor: Mastranzo V.M., Yuste F., Sánchez-Obregón R., Ortiz B., et al.2009ArkivocScopus-id: 2-s2.0-77951874401
01
15Mild and general method for the synthesis of sulfonamidesCoautor: Mastranzo V.M., Ruano, JLG, Parra A., Yuste F.2008Synthesis-StuttgartWoS-id: 000252846900020
Scopus-id: 2-s2.0-38849091996
5633
16Determination 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 group1ᵉʳ autor: Mastranzo V.M., Quintero L., De Parrodi C.A.2007ChiralityWoS-id: 000247128300011
Scopus-id: 2-s2.0-34250214123
87
17Synthesis of chiral ligands containing the N-(S)-a-phenylethyl group and their evaluation as activators in the enantioselective addition of Et2Zn to benzaldehyde1ᵉʳ autor: Mastranzo V.M., Santacruz E., Huelgas G., Paz E., et al.2006TETRAHEDRON-ASYMMETRYWoS-id: 000239522700010
Scopus-id: 2-s2.0-33745809479
1417
18Use of diamines containing the a-phenylethyl group as chiral ligands in the asymmetric hydrosilylation of prochiral ketones1ᵉʳ autor: Mastranzo V.M., Quintero L., De Parrodi C.A., Juaristi E., et al.2004TetrahedronWoS-id: 000188944400007
Scopus-id: 2-s2.0-0842310704
8285

Docencia Impartida

# Entidad Nivel Asignatura Año Semestre Alumnos
1Facultad de QuímicaMaestríaTEMAS SELECTOS20122012-25

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