González Soengas, Raquel María Autor

Stereoselective Synthesis of Carbohydrate-Derived N-Sulfonyl Aziridines

  • Rodríguez-Solla, H.
  • Concellón, C.
  • Alvaredo, N.
  • Llavona, R.
  • García-Granda, S.
  • Díaz, M.R.
  • Soengas, R.
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Synlett - 1/1/2013

10.1055/s-0032-1317954

Número de citas: 6 (Web of Science) 7 (Scopus)

Preparation of sugar derived β,β′-dihydroxy α,α-disubstituted α-amino acids

  • Soengas, R.G.
  • Estévez, A.M.
  • Estévez, J.C.
  • Estévez, R.J.

Tetrahedron Asymmetry - 15/9/2012

10.1016/j.tetasy.2012.08.003

Número de citas: 3 (Web of Science) 3 (Scopus)

Synthesis of Sugar-Derived 2-Nitroalkanols via Henry Reaction Promoted by Samarium Diiodide or Indium

  • Rodríguez-Solla, H.
  • Alvaredo, N.
  • Soengas, R.

Synlett - 13/8/2012

10.1055/s-0031-1290441

Número de citas: 16 (Web of Science) 15 (Scopus)

Indium-Mediated Aza-Henry Reaction of Imines: Access to 2-Nitroamines

  • Soengas, R.G.
  • Silva, S.
  • Estévez, A.M.
  • Estévez, J.C.
  • Estévez, R.J.
  • Rodríguez-Solla, H.

European Journal of Organic Chemistry - 1/8/2012

10.1002/ejoc.201200304

Número de citas: 13 (Web of Science) 13 (Scopus)
Open Access

Indium-mediated allylation and Reformatsky reaction on glyoxylic oximes under ultrasound irradiation

  • Soengas, R.G.
  • Estévez, A.M.

Ultrasonics Sonochemistry - 1/7/2012

10.1016/j.ultsonch.2011.11.012

Número de citas: 8 (Web of Science) 8 (Scopus)

Hydroxymethyl-Branched Piperidines from Hydroxymethyl-Branched Lactones: Synthesis and Biological Evaluation of 1,5-Dideoxy-2-C-hydroxymethyl-1,5-imino-D-mannitol, 1,5-Dideoxy-2-C-hydroxymethyl-1,5-imino-L-gulitol and 1,5-Dideoxy-2-C-hydroxymethyl-1,5-imino-D-talitol

  • Soengas, R.G.
  • Simone, M.I.
  • Hunter, S.
  • Nash, R.J.
  • Evinson, E.L.
  • Fleet, G.W.J.

European Journal of Organic Chemistry - 1/4/2012

10.1002/ejoc.201200054

Número de citas: 20 (Web of Science) 18 (Scopus)

Indium-Catalyzed Henry-Type Reaction of Aldehydes with Bromonitroalkanes

  • Soengas, R.G.
  • Silva, A.M.S.

Synlett - 16/3/2012

10.1055/s-0031-1290617

Número de citas: 26 (Web of Science) 24 (Scopus)

Synthesis of three branched iminosugars [(3R,4R,5S)-3-(hydroxymethyl)piperidine-3,4,5-triol, (3R,4R,5R)-3-(hydroxymethyl)piperidine-3,4,5-triol and (3S,4R,5R)-3-(hydroxymethyl)piperidine-3.4,5-triol] and a branched trihydroxynipecotic acid [(3R,4R,5R)-3,4,5-trihydroxypiperidine-3-carboxylic acid] from sugar lactones with a carbon substituent at C-2

  • Simone, M.I.
  • Soengas, R.G.
  • Jenkinson, S.F.
  • Evinson, E.L.
  • Nash, R.J.
  • Fleet, G.W.J.

Tetrahedron Asymmetry - 15/3/2012

10.1016/j.tetasy.2012.03.007

Número de citas: 21 (Web of Science) 18 (Scopus)

The use of samarium or sodium iodide salts as an alternative for the aza-Henry reaction

  • Rodríguez-Solla, H.
  • Concellón, C.
  • Alvaredo, N.
  • Soengas, R.G.

TETRAHEDRON - 11/2/2012

10.1016/j.tet.2011.12.061

Número de citas: 25 (Web of Science) 24 (Scopus)

Indium-mediated reaction of nitroethane and aldehydes: characterization of the nucleophilic organoindium species

  • Soengas, R.G.
  • Estévez, A.M.

Tetrahedron Letters - 1/2/2012

10.1016/j.tetlet.2011.11.094

Número de citas: 17 (Web of Science) 17 (Scopus)

Recent Advances in the Chemistry and Biology of Spirocyclic Nucleosides

  • Soto, Martín
  • Rodríguez-Solla, Humberto
  • Soengas, Raquel

Topics in Heterocyclic Chemistry - 2019

10.1007/7081_2019_31

  • ORCID

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

10.1002/9781119044222.ch3

Número de citas: 1 (Scopus)

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

Número de citas:
  • Dialnet

An overview on the synthesis of sugar imino acids

  • Soengas R.
  • Estévez A.

TARGETS IN HETEROCYCLIC SYSTEMS: CHEMISTRY AND PROPERTIES, VOL 13 (2009) - 1/1/2011

Número de citas:

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

Número de citas:
  • Dialnet

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

10.1007/978-3-031-51452-4_23

Número de citas:

A gold(III) complex, a conjugate of the gold(III) complex, a pharmaceutical composition comprising the gold(III) complex and uses and a process for preparing the gold(III) complex

  • Soengas, Raquel

29/04/2019

  • 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
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ChemRxiv - 20/01/2020

10.26434/chemrxiv.11619873.v1

  • 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
... Ver más Contraer

20/01/2020

10.26434/chemrxiv.11619873

  • ORCID

Scopus: 19

Web of Science: 22

Scopus: 42

Web of Science: 50

Última actualización de los datos: 20/04/24 8:54
Próxima recolección programada: 27/04/24 3:00