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Mota Ávila, Antonio José Autor

Comparative study of the oxidative degradation of different 4-Aminobenzene sulfonamides in aqueous solution by sulfite activation in the presence of Fe(0), Fe(II), Fe(III) or Fe(VI)

  • Acosta-Rangel A.
  • Sánchez-Polo M.
  • Rozalen M.
  • Rivera-Utrilla J.
  • Polo A.
  • Mota A.

Water (Switzerland) - 1/11/2019

10.3390/w11112332

Número de citas: 9 (Web of Science) 5 (Scopus)
  • Cuartil SJR: Q1
  • Categorías SJR: Geography, Planning and Development (Q1); Aquatic Science (Q2); Water Science and Technology (Q2); Biochemistry (Q3)

Highly efficient synthesis of 2?,3?-didehydro-2?, 3?-dideoxy-?-nucleosides through a sulfur-mediated reductive 2?,3?-trans-elimination. From iodomethylcyclopropanes to thiirane analogs

  • De Cienfuegos L.
  • Mota A.
  • Rodríguez C.
  • Robles R.

Tetrahedron Letters - 17/1/2005

10.1016/j.tetlet.2004.11.087

Número de citas: 6 (Web of Science) 8 (Scopus)
  • Cuartil SJR: Q1
  • CiteScore: 4,3 (2020)
  • SJR: 1,26 (2005)
  • SNIP: 0,935 (2005)
  • Categorías SJR: Drug Discovery (Q1); Organic Chemistry (Q1); Biochemistry (Q2)

Thermodynamic and kinetic considerations in the chemoselective O-acylation by mixed anhydrides. A semiempirical MO approach

  • Mota A.
  • Robles R.
  • De Cienfuegos L.
  • Lamenca A.

Tetrahedron Letters - 19/4/2004

10.1016/j.tetlet.2004.03.045

Número de citas: 2 (Web of Science) 3 (Scopus)
  • Cuartil SJR: Q1
  • CiteScore: 4,3 (2020)
  • SJR: 1,3 (2004)
  • SNIP: 0,957 (2004)
  • Categorías SJR: Drug Discovery (Q1); Organic Chemistry (Q1); Biochemistry (Q2)

Ring-opening of N-alkoxycarbonyl ?-lactams with lithium methylphenylsulphone: Application to the synthesis of cis 2,5-disubstituted pyrrolidines

  • Mota A.
  • Langlois N.

Tetrahedron Letters - 3/2/2003

10.1016/s0040-4039(02)02839-3

Número de citas: 17 (Web of Science) 18 (Scopus)
  • Cuartil SJR: Q1
  • CiteScore: 4,3 (2020)
  • SJR: 1,312 (2003)
  • SNIP: 0,98 (2003)
  • Categorías SJR: Biochemistry (Q1); Drug Discovery (Q1); Organic Chemistry (Q1)

Highly stereocontrolled alkylation of protected 'diacetone hexulose aldehydes'

  • Izquierdo I.
  • Plaza M.
  • Robles R.
  • Mota A.
  • Franco F.

Tetrahedron Asymmetry - 30/10/2001

10.1016/s0957-4166(01)00488-8

Número de citas: 19 (Web of Science) 19 (Scopus)
  • Cuartil SJR: Q1
  • CiteScore: 4,7 (2019)
  • SJR: 1,54 (2001)
  • SNIP: 1,034 (2001)
  • Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)

A new and highly stereoselective synthesis of polyhydroxyindolizidines from 4-octulose derivatives

  • Izquierdo I.
  • Plaza M.
  • Robles R.
  • Mota A.

Tetrahedron Asymmetry - 27/3/1998

10.1016/s0957-4166(98)00064-0

Número de citas: 27 (Web of Science) 29 (Scopus)
  • CiteScore: 4,7 (2019)

An efficient and highly stereoselective synthesis of nucleoside derivatives from furanoid 1,2-diols

  • Robles R.
  • Rodríguez C.
  • Izquierdo I.
  • Plaza M.
  • Mota A.

Tetrahedron Asymmetry - 11/9/1997

10.1016/s0957-4166(97)00332-7

Número de citas: 24 (Web of Science) 23 (Scopus)
  • CiteScore: 4,7 (2019)

Highly ?-stereoselective nucleosidation from ?-D-xylo- and ?-D-ribo-furanose 1,2-thiocarbonates

  • Robles R.
  • Rodríguez C.
  • Álvarez De Cienfuegos L.
  • Mota A.

Tetrahedron Asymmetry - 8/3/2004

10.1016/j.tetasy.2003.12.037

Número de citas: 7 (Web of Science) 7 (Scopus)
  • Cuartil SJR: Q1
  • CiteScore: 4,7 (2019)
  • SJR: 1,313 (2004)
  • SNIP: 0,971 (2004)
  • Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)

Preparation of 2,2’-anhydronucleosides: Regio- and stereoselective modifications of the base and sugar moieties

  • Robles R.
  • Rodríguez C.
  • Izquierdo I.
  • Plaza M.
  • Mota A.
  • De Cienfuegos L.

Tetrahedron Asymmetry - 11/8/2000

10.1016/s0957-4166(00)00272-x

Número de citas: 15 (Web of Science) 15 (Scopus)
  • Cuartil SJR: Q1
  • CiteScore: 4,7 (2019)
  • SJR: 1,782 (2000)
  • SNIP: 1,015 (2000)
  • Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)

Semiempirical MO approach to the mechanism of the NIS-mediated nucleophilic addition to glycals: Multicomponent intermediates as models to tackle reactivity in organic chemistry

  • Mota A.
  • Castellanos E.
  • Álvarez De Cienfuegos L.
  • Robles R.

Tetrahedron Asymmetry - 2/5/2005

10.1016/j.tetasy.2005.03.010

Número de citas: 6 (Web of Science) 6 (Scopus)
  • Cuartil SJR: Q1
  • CiteScore: 4,7 (2019)
  • SJR: 1,297 (2005)
  • SNIP: 0,905 (2005)
  • Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)

Application of the DFT Method to the Study of Intramolecular Palladium Shifts in Aryl and Polyaryl Complexes

  • Dedieu A.
  • Mota A.

Computational Methods in Catalysis and Materials Science: An Introduction for Scientists and Engineers - 24/6/2009

10.1002/9783527625482.ch16

Número de citas:

Salt effects on the conformational behavior of 5-substituted 1,3-dioxanes

  • Juaristi E.
  • Rosquete-Pina G.A.
  • Vázquez-Hernández M.
  • Mota A.J.

Pure and Applied Chemistry - 1/5/2003

10.1351/pac200375050589

Número de citas: 17 (Web of Science) 15 (Scopus)
  • CiteScore: 3,6 (2020)
  • SJR: 0,836 (2003)
  • SNIP: 0,975 (2003)

Este autor no tiene patentes.

Erratum: Semiempirical MO approach to the mechanism of the NIS-mediated nucleophilic addition to glycals: Multicomponent intermediates as models to tackle reactivity in organic chemistry (Tetrahedron: Asymmetry (2005) 16 (1615) DOI: 10.1016/j.tetasy.2005.03.010)

  • Mota A.
  • Castellanos E.
  • De Cienfuegos L.
  • Robles R.

Tetrahedron Asymmetry - 4/7/2005

10.1016/j.tetasy.2005.06.019

Número de citas:
  • Cuartil SJR: Q1
  • CiteScore: 4,7 (2019)
  • SJR: 1,297 (2005)
  • SNIP: 0,905 (2005)
  • Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)

Erratum: Anion encapsulation promoted by anion?? interactions in rationally designed hexanuclear antiferromagnetic wheels: Synthesis, structure and magnetic properties (CrystEngComm (2009) 11 (2054-2064) DOI: 10.1039/b906382j)

  • Colacio E.
  • Aouryaghal H.
  • Mota A.
  • Cano J.
  • Sillanpää R.
  • Rodríguez-Diéguez A.

CrystEngComm - 28/12/2009

10.1039/b922492k

Número de citas:
  • Cuartil SJR: Q1
  • Factor Impacto JCR: 4,183 (null)
  • CiteScore: 5,5 (2020)
  • SJR: 1,273 (2009)
  • SNIP: 1,307 (2009)
  • Impacto JCR a 5 años: 4,076
  • Categorías JCR: CRYSTALLOGRAPHY
  • Categorías SJR: Chemistry (miscellaneous) (Q1); Condensed Matter Physics (Q1); Materials Science (miscellaneous) (Q1)

Scopus: 29

Web of Science: 31

Scopus: 75

Web of Science: 76

Última actualización de los datos: 1/04/23 21:31
Próxima recolección programada: 8/04/23 3:00