González Soengas, Raquel María Autor
Studies on the transformation of nitrosugars into branched chain iminosugars. Part II: Synthesis of (3R,4R,5R,6S)-2,2-bis(hydroxymethyl)azepane-3,4,5,6-tetraol
- Otero, J.M.
- Estévez, A.M.
- Soengas, R.G.
- Estévez, J.C.
- Nash, R.J.
- Fleet, G.W.J.
- Estévez, R.J.
Tetrahedron Asymmetry - 3/11/2008
- Cuartil SJR: Q1
- CiteScore: 4,7 (2019)
- SJR: 1,511 (2008)
- SNIP: 0,851 (2008)
- Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)
- Scopus
- ORCID
- Web of Science
Total synthesis of (-)-dysithiazolamide
- Ardá, A.
- Soengas, R.G.
- Nieto, M.I.
- Jiménez, C.
- Rodríguez, J.
Organic Letters - 5/6/2008
- Cuartil SJR: Q1
- CiteScore: 10,2 (2020)
- SJR: 3,319 (2008)
- SNIP: 1,3 (2008)
- Categorías SJR: Biochemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1)
- Scopus
- ORCID
- Web of Science
Ethyl 1-O-tert-butyl-dimethylsilyl-2,3-O-isopropylidene-5-[(2'S)- tetrahydropyran-2-yloxy]-D-glycero-a-d-manno-heptofuronate
- Soengas, R.G.
- Valencia, L.
- Estévez, J.C.
- Estévez, R.J.
Acta Crystallographica Section E: Structure Reports Online - 15/8/2008
- Cuartil SJR: Q2
- CiteScore: 0,8 (2016)
- SJR: 0,287 (2008)
- SNIP: 0,457 (2008)
- Categorías SJR: Materials Science (miscellaneous) (Q2); Chemistry (miscellaneous) (Q3); Condensed Matter Physics (Q3)
- Scopus
- ORCID
- Web of Science
Indium-mediated Reformatsky reaction on lactones: preparation of 2-deoxy-2,2'-dimethyl-3-ulosonic acids
- Soengas, R.G.
TETRAHEDRON LETTERS - 6/1/2010
- Cuartil SJR: Q1
- Factor Impacto JCR: 2,618 (2010)
- CiteScore: 4,3 (2020)
- SJR: 1,245 (2010)
- SNIP: 0,901 (2010)
- Impacto JCR a 5 años: 2,483
- Categorías JCR: CHEMISTRY, ORGANIC
- Categorías SJR: Drug Discovery (Q1); Organic Chemistry (Q1); Biochemistry (Q2)
- Scopus
- ORCID
- Web of Science
Studies on the stereocontrolled transformation of nitrohexofuranoses into 2-oxabicyclo[2.2.1]heptanes. V: Synthesis of enantiopure methyl (1R,2R,4S)-2-amino-4-hydroxycyclopentanecarboxylate
- Estévez, A.
- Soengas, R.G.
- Tato, R.
- Thomas, P.
- Estévez, J.C.
- Estévez, R.J.
- Sussman, F.
TETRAHEDRON-ASYMMETRY - 29/1/2010
- Cuartil SJR: Q1
- Factor Impacto JCR: 2,484 (2010)
- CiteScore: 4,7 (2019)
- SJR: 1,301 (2010)
- SNIP: 0,9 (2010)
- Impacto JCR a 5 años: 2,53
- Categorías JCR: CHEMISTRY, PHYSICAL
- Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)
- Scopus
- ORCID
- Web of Science
Studies on the transformation of nitrosugars into iminosugars III: synthesis of (2R,3R,4R,5R,6R)-2-(hydroxymethyl)azepane-3,4,5,6-tetraol and (2R,3R,4R,5R,6S)-2-(hydroxymethyl)azepane-3,4,5,6-tetraol
- Estévez, A.M.
- Soengas, R.G.
- Otero, J.M.
- Estévez, J.C.
- Nash, R.J.
- Estévez, R.J.
TETRAHEDRON-ASYMMETRY - 29/1/2010
- Cuartil SJR: Q1
- Factor Impacto JCR: 2,484 (2010)
- CiteScore: 4,7 (2019)
- SJR: 1,301 (2010)
- SNIP: 0,9 (2010)
- Impacto JCR a 5 años: 2,53
- Categorías JCR: CHEMISTRY, PHYSICAL
- Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)
- Scopus
- ORCID
- Web of Science
Convenient procedure for the indium-mediated hydroxymethylation of active bromo compounds: Transformation of ketones into a-hydroxymethyl nitroalkanes
- Soengas, R.G.
- Estévez, A.M.
SYNLETT - 15/10/2010
- Cuartil SJR: Q1
- Factor Impacto JCR: 2,447 (2010)
- CiteScore: 4,2 (2020)
- SJR: 1,241 (2010)
- SNIP: 0,652 (2010)
- Impacto JCR a 5 años: 2,343
- Categorías JCR: CHEMISTRY, ORGANIC
- Categorías SJR: Organic Chemistry (Q1)
- Scopus
- ORCID
- Web of Science
A straightforward route to novel a,a-disubstituted tetrahydrofuran ß-amino acids and spirodiketopiperazines from sugar lactones
- Soengas, R.G.
SYNLETT - 15/10/2010
- Cuartil SJR: Q1
- Factor Impacto JCR: 2,447 (2010)
- CiteScore: 4,2 (2020)
- SJR: 1,241 (2010)
- SNIP: 0,652 (2010)
- Impacto JCR a 5 años: 2,343
- Categorías JCR: CHEMISTRY, ORGANIC
- Categorías SJR: Organic Chemistry (Q1)
- Scopus
- ORCID
- Web of Science
Indium-mediated reaction of 1-bromo-1-nitroalkanes with aldehydes: Access to 2-nitroalkan-1-ols
- Soengas, R.G.
- Estévez, A.M.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY - 1/9/2010
- Cuartil SJR: Q1
- Factor Impacto JCR: 3,206 (2010)
- CiteScore: 5,2 (2020)
- SJR: 1,615 (2010)
- SNIP: 0,843 (2010)
- Impacto JCR a 5 años: 2,996
- Categorías JCR: CHEMISTRY, ORGANIC
- Categorías SJR: Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1)
- Scopus
- ORCID
- Web of Science
Studies on indium-mediated additions to lactones: Synthesis of 2-deoxy-2-substituted-3-ulosonic acids
- Soengas, R.G.
TETRAHEDRON-ASYMMETRY - 27/9/2010
- Cuartil SJR: Q1
- Factor Impacto JCR: 2,484 (2010)
- CiteScore: 4,7 (2019)
- SJR: 1,301 (2010)
- SNIP: 0,9 (2010)
- Impacto JCR a 5 años: 2,53
- Categorías JCR: CHEMISTRY, PHYSICAL
- Categorías SJR: Inorganic Chemistry (Q1); Organic Chemistry (Q1); Physical and Theoretical Chemistry (Q1); Catalysis (Q2)
- Scopus
- ORCID
- Web of Science
Nuevas estrategias de síntesis de "Alfa"-, "Beta"- y "Gamma"-aminoácidos polihidroxilados y compuestos relacionados: reacción de Henry, alquilación intramolecular y heteroanulación de monosacáridos
- Raquel González Soengas
- Ramón José Estévez Cabanas
- Juan Carlos Estévez Cabanas
2003
- Dialnet
Recent advances in nitro sugar chemistry
- Soengas, Raquel G.
- Estevez, Juan C.
- Estevez, Amalia M.
- Fernandez, Fernando
- Estevez, Ramon J.
- Rauter, AP
- Lindhorst, TK
CARBOHYDRATE CHEMISTRY: CHEMICAL AND BIOLOGICAL APPROACHES, VOL 35 - 2009
- ORCID
- Web of Science
Nuevas aplicaciones sintéticas de los nitroazúcares y del ácido siquímico: b- y g-aminoácidos e iminoazúcares
- Amalia Estévez Reino
- Ramón José Estévez Cabanas
- Juan Carlos Estévez Cabanas
- Raquel González Soengas
2011
- Dialnet
An overview of key routes for the transformation of sugars into carbasugars and related compounds
- Soengas, R.G.
- Otero, J.M.
- Estévez, A.M.
- Rauter, A.P.
- Cachatra, V.
- Estévez, J.C.
- Estévez, R.J.
Carbohydrate Chemistry - 1/12/2012
- Cuartil SJR: Q4
- CiteScore: 2,6 (2020)
- SJR: 0,127 (2012)
- SNIP: 0,073 (2012)
- Categorías SJR: Biochemistry (Q4); Organic Chemistry (Q4)
- Scopus
- ORCID
- Web of Science
Reductive Ring-Opening in Domino Reactions of Carbohydrates
- Soengas, R.G.
- Tomé, S.M.
- Silva, A.M.S.
Domino and Intramolecular Rearrangement Reactions as Advanced Synthetic Methods in Glycoscience - 15/1/2016
- Scopus
- ORCID
ChemXP AR Edition, A Serious Game
- Bandeira M.
- Vairinhos M.
- Dias P.
- Soengas R.
- Silva V.
Communications in Computer and Information Science - 1/1/2024
- CiteScore: 1 (2022)
- SJR: 0,194 (2022)
- SNIP: 0,241 (2022)
Chlorosphaerolactylates A-D: The Natural Chlorinated Lactylates Isolated from the Portuguese Cyanobacterium Sphaerospermopsis Sp. LEGE 00249
- Ignacio Gutiérrez-del-Río
- Nelly B. de Fraissinette
- Raquel Castelo-Branco
- Flavio Oliveira
- João Morais
- Saúl Redondo-Blanco
- Claudio J. Villar
- María José Iglesias
- Raquel G. Soengas
- Virginio Cepas
- Yuly López Cubillos
- Giacomo Sampietro
- Liliana Rodolfi
- Felipe Lombó
- Sara M. Soto González
- Fernando López Ortiz
- Vitor M. Vasconcelos
- Mariana Reis
ChemRxiv - 20/01/2020
- ORCID
Chlorosphaerolactylates A-D: The Natural Chlorinated Lactylates Isolated from the Portuguese Cyanobacterium Sphaerospermopsis Sp. LEGE 00249
- Ignacio Gutiérrez-del-Río
- Nelly B. de Fraissinette
- Raquel Castelo-Branco
- Flavio Oliveira
- João Morais
- Saúl Redondo-Blanco
- Claudio J. Villar
- María José Iglesias
- Raquel G. Soengas
- Virginio Cepas
- Yuly López Cubillos
- Giacomo Sampietro
- Liliana Rodolfi
- Felipe Lombó
- Sara M. Soto González
- Fernando López Ortiz
- Vitor M. Vasconcelos
- Mariana Reis
20/01/2020
- ORCID
Información de contacto
Departamento: Química y Física
Correo electrónico: rsoengas@ual.es
Índice h
Scopus: 19
Web of Science: 22
Índice i10
Scopus: 42
Web of Science: 50
Grupos de investigación
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Química orgánica y organometálica
Rol: Miembro
Perfiles de autor
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Proyectos de investigación en la UAL
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Acrónimo NOMORFILMDesde: 1 de abril de 2015Hasta: 31 de diciembre de 2019Financiado por: NaNImporte de financiación: 358.031,25 EURRol: Partner