ROBERTO CARLOS MELGAR FERNANDEZ



DATOS GENERALES NOMBRAMIENTOS
Nombre completo   ROBERTO CARLOS MELGAR FERNANDEZ
Máximo nivel de estudios  
Antigüedad académica en la UNAM   años, meses, días

Último 
ESTIMULOS, PROGRAMAS, PREMIOS Y RECONOCIMIENTOS
* SNI C2014 - 2018

INFORMACIÓN DE PUBLICACIONES
Firmas  
Melgar-Fernández R. MelgarFernandez, R
ID's SCOPUS  
8511935300
Áreas de conocimiento  
Chemistry, medicinal Chemistry, multidisciplinary Chemistry, organic Chemistry, physical Scie jcr
Chemistry (miscellaneous) Organic Chemistry
Coautorías con entidades de la UNAM  
Revistas en las que ha publicado  (8):
  1. Arkivoc, Estados Unidos America (2010)
  2. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, Reino Unido (2004)
  3. JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, Países Bajos (2015)
  4. JOURNAL OF ORGANIC CHEMISTRY, Estados Unidos America (2007)
  5. JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Estados Unidos America (2005)
  6. Journal Of The Mexican Chemical Society, México (2009)
  7. Tetrahedron, Reino Unido (2004, 2005)
  8. TETRAHEDRON LETTERS, Reino Unido (2005)


Documentos indexados (WoS y Scopus)

# Título del documento Autores Año Rista Fuente Citas WoS Citas Scopus
1Chiral recognition of abacavir enantiomers by (2-hydroxy)propyl-beta-cyclodextrin: UHPLC, NMR and DFT studiesCoautor: MelgarFernandez, R, ReyesReyes, ML, RoaMorales, G, ReyesPerez, H, et al.2015JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRYWoS-id: 000357572400008
Scopus-id: 2-s2.0-84943223327
1211
2Resolution of 5-oxo-1-phenylpyrazolidine-3-carboxylic acid and synthesis of novel enantiopure amide derivatives1ᵉʳ autor: Melgar-Fernández R., González-Olvera R., Vargas-Caporali J., Pérez-Isidoro R., et al.2010ArkivocWoS-id: 000282479600007
Scopus-id: 2-s2.0-77953373183
44
3Optimized Methodologies in Asymmetric Organic Synthesis Applying Microwaves2ᵒ autor: Melgar-Fernández R., Bandala Y., Guzmán-Mejía R., Olivares-Romero J.L., et al.2009Journal Of The Mexican Chemical SocietyWoS-id: 000274885500012
Scopus-id: 2-s2.0-77953193427
77
4Enantioselective amination of a-phenyl-a-cyanoacetate catalyzed by chiral amines incorporating the a-phenylethyl auxiliary2ᵒ autor: Melgar-Fernández R., Liu Y., Juaristi E.2007JOURNAL OF ORGANIC CHEMISTRYWoS-id: 000244071100068
Scopus-id: 2-s2.0-33846957747
3843
5Synthesis of 2-substituted-5-halo-2,3-dihydro-4(H)-pyrimidin-4-ones and their derivatization utilizing the sonogashira coupling reaction in the enantioselective synthesis of a-substituted ß-amino acidsCoautor: Melgar-Fernández R., Díaz-Sánchez B.R., Iglesias-Arteaga M.A., Juaristi E.2007JOURNAL OF ORGANIC CHEMISTRYWoS-id: 000247246100027
Scopus-id: 2-s2.0-34250817420
3742
6Erratum: "enantioselective protonation of prochiral enolates in the asymmetric synthesis of (S)-naproxen": [Tetrahedron Lett. 44 (2003) 2023] (Tetrahedron Letters (2003) 44 (2023) DOI: 10.1016/S0040-4039(03)00217-X)1ᵉʳ autor: Melgar-Fernández R., Juaristi E.2005TETRAHEDRON LETTERSWoS-id: 000226846800040
Scopus-id: 2-s2.0-12344308284
22
7Erratum: Enantioselective alkylation and protonation of prochiral enolates in the asymmetric synthesis of ß-amino acids (Tetrahedron (2003) 59 (4223) DOI: 10.1016/S0040-4020(03)00578-7)1ᵉʳ autor: Melgar-Fernández R., González-Olvera R., Juaristi E.2005TetrahedronWoS-id: 000228417100014
Scopus-id: 2-s2.0-16244380814
44
8Synthesis and conformational analysis of chiral ureas incorporating N-1-phenylethyl groups. Manifestation ofallylic 1,3-strain2ᵒ autor: Melgar-Fernández R., Hernández-Rodríguez M., Juaristi E.2005JOURNAL OF PHYSICAL ORGANIC CHEMISTRYWoS-id: 000230711900015
Scopus-id: 2-s2.0-22544488137
1515
9Synthesis and cardiovascular activity of metoprolol analogues1ᵉʳ autor: Melgar-Fernández R., Demare P., Hong E., Rosas M.A., et al.2004BIOORGANIC & MEDICINAL CHEMISTRY LETTERSWoS-id: 000187862000038
Scopus-id: 2-s2.0-18344412781
45
10Cis- and trans-N-(Benzylsulfinyl)hexahydrobenzoxazolidin-2-ones as novel chiral sulfinyl transfer reagentsCoautor: Melgar-Fernández R., Clara-Sosa A., Pérez L., Sánchez M., et al.2004TetrahedronWoS-id: 000225525700012
Scopus-id: 2-s2.0-9644269060
98

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