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Catalytic Diastereo- and Enantioselective Synthesis of 2-Imidazolinones.

Organic letters

Martínez-Pardo P, Blay G, Escrivá-Palomo A, Sanz-Marco A, Vila C, Pedro JR.
PMID: 31090430
Org Lett. 2019 Jun 07;21(11):4063-4066. doi: 10.1021/acs.orglett.9b01244. Epub 2019 May 15.

Chiral cyclic ureas (2-imidazolinones) were prepared by the reaction of nitrones and isocyanoacetate esters using a multicatalytic system that combines a bifunctional Brønsted base-squaramide organocatalyst and Ag

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Martínez-Pardo P, Blay G, Escrivá-Palomo A, et al. Catalytic Diastereo- and Enantioselective Synthesis of 2-Imidazolinones. Org Lett. 2019;21(11):4063-4066doi: 10.1021/acs.orglett.9b01244.
Martínez-Pardo, P., Blay, G., Escrivá-Palomo, A., Sanz-Marco, A., Vila, C., & Pedro, J. R. (2019). Catalytic Diastereo- and Enantioselective Synthesis of 2-Imidazolinones. Organic letters, 21(11), 4063-4066. https://doi.org/10.1021/acs.orglett.9b01244
Martínez-Pardo, Pablo, et al. "Catalytic Diastereo- and Enantioselective Synthesis of 2-Imidazolinones." Organic letters vol. 21,11 (2019): 4063-4066. doi: https://doi.org/10.1021/acs.orglett.9b01244
Martínez-Pardo P, Blay G, Escrivá-Palomo A, Sanz-Marco A, Vila C, Pedro JR. Catalytic Diastereo- and Enantioselective Synthesis of 2-Imidazolinones. Org Lett. 2019 Jun 07;21(11):4063-4066. doi: 10.1021/acs.orglett.9b01244. Epub 2019 May 15. PMID: 31090430.
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Long-term follow-up with filter paper samples in patients with propionic acidemia.

JIMD reports

Stanescu S, Belanger-Quintana A, Fernández-Felix BM, Pérez-Cerdá C, Merinero B, Ruiz-Sala P, Arrieta F, Martínez-Pardo M.
PMID: 33473339
JIMD Rep. 2020 Sep 27;57(1):44-51. doi: 10.1002/jmd2.12166. eCollection 2021 Jan.

BACKGROUND: Propionic acidemia (PA) is an inherited disorder caused by deficiency of propionyl CoA carboxylase. Most patients with this disorder are diagnosed during the neonatal period because of severe metabolic acidosis and hyperammonemia. Patients are required to undergo blood...

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Stanescu S, Belanger-Quintana A, Fernández-Felix BM, et al. Long-term follow-up with filter paper samples in patients with propionic acidemia. JIMD Rep. 2020;57(1):44-51doi: 10.1002/jmd2.12166.
Stanescu, S., Belanger-Quintana, A., Fernández-Felix, B. M., Pérez-Cerdá, C., Merinero, B., Ruiz-Sala, P., Arrieta, F., & Martínez-Pardo, M. (2021). Long-term follow-up with filter paper samples in patients with propionic acidemia. JIMD reports, 57(1), 44-51. https://doi.org/10.1002/jmd2.12166
Stanescu, Sinziana, et al. "Long-term follow-up with filter paper samples in patients with propionic acidemia." JIMD reports vol. 57,1 (2021): 44-51. doi: https://doi.org/10.1002/jmd2.12166
Stanescu S, Belanger-Quintana A, Fernández-Felix BM, Pérez-Cerdá C, Merinero B, Ruiz-Sala P, Arrieta F, Martínez-Pardo M. Long-term follow-up with filter paper samples in patients with propionic acidemia. JIMD Rep. 2020 Sep 27;57(1):44-51. doi: 10.1002/jmd2.12166. eCollection 2021 Jan. PMID: 33473339; PMCID: PMC7802619.
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Thermoplastic starch-nanohybrid films with polyhedral oligomeric silsesquioxane.

Carbohydrate polymers

Martinez-Pardo I, Shanks RA, Adhikari B, Adhikari R.
PMID: 28732856
Carbohydr Polym. 2017 Oct 01;173:170-177. doi: 10.1016/j.carbpol.2017.05.009. Epub 2017 May 10.

Thermoplastic starch forms packaging films that have low gas permeability, but they are more permeable to water vapour and they are attacked by water. Our approach was to create surface and internal localised hydrophobicity using added reactive nano-materials to...

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Martinez-Pardo I, Shanks RA, Adhikari B, et al. Thermoplastic starch-nanohybrid films with polyhedral oligomeric silsesquioxane. Carbohydr Polym. 2017;173:170-177doi: 10.1016/j.carbpol.2017.05.009.
Martinez-Pardo, I., Shanks, R. A., Adhikari, B., & Adhikari, R. (2017). Thermoplastic starch-nanohybrid films with polyhedral oligomeric silsesquioxane. Carbohydrate polymers, 173170-177. https://doi.org/10.1016/j.carbpol.2017.05.009
Martinez-Pardo, I, et al. "Thermoplastic starch-nanohybrid films with polyhedral oligomeric silsesquioxane." Carbohydrate polymers vol. 173 (2017): 170-177. doi: https://doi.org/10.1016/j.carbpol.2017.05.009
Martinez-Pardo I, Shanks RA, Adhikari B, Adhikari R. Thermoplastic starch-nanohybrid films with polyhedral oligomeric silsesquioxane. Carbohydr Polym. 2017 Oct 01;173:170-177. doi: 10.1016/j.carbpol.2017.05.009. Epub 2017 May 10. PMID: 28732856.
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Brevioxime: A New Juvenile Hormone Biosynthesis Inhibitor Isolated from Penicillium brevicompactum.

The Journal of organic chemistry

Moya P, Castillo M, Primo-Yúfera E, Couillaud F, Martínez-Máñez R, Garcerá MD, Miranda MA, Primo J, Martínez-Pardo R.
PMID: 11671999
J Org Chem. 1997 Nov 28;62(24):8544-8545. doi: 10.1021/jo970397y.

No abstract available.

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Moya P, Castillo M, Primo-Yúfera E, et al. Brevioxime: A New Juvenile Hormone Biosynthesis Inhibitor Isolated from Penicillium brevicompactum. J Org Chem. 1997;62(24):8544-8545doi: 10.1021/jo970397y.
Moya, P., Castillo, M., Primo-Yúfera, E., Couillaud, F., Martínez-Máñez, R., Garcerá, M. D., Miranda, M. A., Primo, J., & Martínez-Pardo, R. (1997). Brevioxime: A New Juvenile Hormone Biosynthesis Inhibitor Isolated from Penicillium brevicompactum. The Journal of organic chemistry, 62(24), 8544-8545. https://doi.org/10.1021/jo970397y
Moya, Pilar, et al. "Brevioxime: A New Juvenile Hormone Biosynthesis Inhibitor Isolated from Penicillium brevicompactum." The Journal of organic chemistry vol. 62,24 (1997): 8544-8545. doi: https://doi.org/10.1021/jo970397y
Moya P, Castillo M, Primo-Yúfera E, Couillaud F, Martínez-Máñez R, Garcerá MD, Miranda MA, Primo J, Martínez-Pardo R. Brevioxime: A New Juvenile Hormone Biosynthesis Inhibitor Isolated from Penicillium brevicompactum. J Org Chem. 1997 Nov 28;62(24):8544-8545. doi: 10.1021/jo970397y. PMID: 11671999.
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[Elaboration, implementation and follow-up of a postmenopausal osteoporosis protocol: Collaboration between the Primary care and Rheumatology departments].

Reumatologia clinica

Madridejos Mora R, Tomás Sanz R, Llobet Traveset E, Gavagnach Bellsolà M, Martínez Pardo S, Moyà Ferrer X.
PMID: 21794698
Reumatol Clin. 2010 May-Jun;6(3):128-33. doi: 10.1016/j.reuma.2009.07.008. Epub 2010 Feb 04.

OBJECTIVE: To improve the clinical management of postmenopausal osteroporosis, an intervention based on the implementation of a guideline agreed to between the Primary Care and Specialized departments of all centers at "Mutua of Terrassa" was carried out.METHODS: Descriptive and...

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Madridejos Mora R, Tomás Sanz R, Llobet Traveset E, et al. Elaboración, implantación y seguimiento de un protocolo de osteoporosis posmenopáusica: colaboración entre Atención Primaria y el Servicio de Reumatología. [Elaboration, implementation and follow-up of a postmenopausal osteoporosis protocol: Collaboration between the Primary care and Rheumatology departments]. Reumatol Clin. 2010;6(3):128-33doi: 10.1016/j.reuma.2009.07.008.
Madridejos Mora, R., Tomás Sanz, R., Llobet Traveset, E., Gavagnach Bellsolà, M., Martínez Pardo, S., & Moyà Ferrer, X. (2010). Elaboración, implantación y seguimiento de un protocolo de osteoporosis posmenopáusica: colaboración entre Atención Primaria y el Servicio de Reumatología. [Elaboration, implementation and follow-up of a postmenopausal osteoporosis protocol: Collaboration between the Primary care and Rheumatology departments]. Reumatologia clinica, 6(3), 128-33. https://doi.org/10.1016/j.reuma.2009.07.008
Madridejos Mora, Rosa, et al. "Elaboración, implantación y seguimiento de un protocolo de osteoporosis posmenopáusica: colaboración entre Atención Primaria y el Servicio de Reumatología." [Elaboration, implementation and follow-up of a postmenopausal osteoporosis protocol: Collaboration between the Primary care and Rheumatology departments]. Reumatologia clinica vol. 6,3 (2010): 128-33. doi: https://doi.org/10.1016/j.reuma.2009.07.008
Madridejos Mora R, Tomás Sanz R, Llobet Traveset E, Gavagnach Bellsolà M, Martínez Pardo S, Moyà Ferrer X. Elaboración, implantación y seguimiento de un protocolo de osteoporosis posmenopáusica: colaboración entre Atención Primaria y el Servicio de Reumatología. [Elaboration, implementation and follow-up of a postmenopausal osteoporosis protocol: Collaboration between the Primary care and Rheumatology departments]. Reumatol Clin. 2010 May-Jun;6(3):128-33. doi: 10.1016/j.reuma.2009.07.008. Epub 2010 Feb 04. Spanish. PMID: 21794698.
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Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis.

Chemical communications (Cambridge, England)

Martínez-Pardo P, Blay G, Muñoz MC, Pedro JR, Sanz-Marco A, Vila C.
PMID: 29488994
Chem Commun (Camb). 2018 Mar 15;54(23):2862-2865. doi: 10.1039/c8cc00856f.

A multicatalytic approach that combines a bifunctional Brønsted base-squaramide organocatalyst and Ag

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Martínez-Pardo P, Blay G, Muñoz MC, et al. Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis. Chem Commun (Camb). 2018;54(23):2862-2865doi: 10.1039/c8cc00856f.
Martínez-Pardo, P., Blay, G., Muñoz, M. C., Pedro, J. R., Sanz-Marco, A., & Vila, C. (2018). Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis. Chemical communications (Cambridge, England), 54(23), 2862-2865. https://doi.org/10.1039/c8cc00856f
Martínez-Pardo, Pablo, et al. "Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis." Chemical communications (Cambridge, England) vol. 54,23 (2018): 2862-2865. doi: https://doi.org/10.1039/c8cc00856f
Martínez-Pardo P, Blay G, Muñoz MC, Pedro JR, Sanz-Marco A, Vila C. Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis. Chem Commun (Camb). 2018 Mar 15;54(23):2862-2865. doi: 10.1039/c8cc00856f. PMID: 29488994.
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Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes.

ChemSusChem

Valiente A, Martínez-Pardo P, Kaur G, Johansson MJ, Martín-Matute B.
PMID: 34738723
ChemSusChem. 2021 Nov 05; doi: 10.1002/cssc.202102221. Epub 2021 Nov 05.

Selective reduction strategies based on abundant-metal catalysts are very important in the production of chemicals. In this paper, a method for the electrochemical semihydrogenation and semideuteration of alkynes to form Z-alkenes was developed, using a simple nickel foam as...

Cite
Valiente A, Martínez-Pardo P, Kaur G, et al. Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem. 2021;doi: 10.1002/cssc.202102221.
Valiente, A., Martínez-Pardo, P., Kaur, G., Johansson, M. J., & Martín-Matute, B. (2021). Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem, . https://doi.org/10.1002/cssc.202102221
Valiente, Alejandro, et al. "Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes." ChemSusChem vol. (2021). doi: https://doi.org/10.1002/cssc.202102221
Valiente A, Martínez-Pardo P, Kaur G, Johansson MJ, Martín-Matute B. Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem. 2021 Nov 05; doi: 10.1002/cssc.202102221. Epub 2021 Nov 05. PMID: 34738723.
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Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America.

Journal of human genetics

Urreizti R, Asteggiano C, Bermudez M, Córdoba A, Szlago M, Grosso C, de Kremer RD, Vilarinho L, D'Almeida V, Martínez-Pardo M, Peña-Quintana L, Dalmau J, Bernal J, Briceño I, Couce ML, Rodés M, Vilaseca MA, Balcells S, Grinberg D.
PMID: 32033511
J Hum Genet. 2007 Apr;52(4):388-389. doi: 10.1007/s10038-006-0103-4.

In this article, one of the novel mutations, c.208_209+ 8del10, was incorrectly given as c.69_70+8del10. It corresponds to patient 64 in Table 4.

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Urreizti R, Asteggiano C, Bermudez M, et al. Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America. J Hum Genet. 2007;52(4):388-389doi: 10.1007/s10038-006-0103-4.
Urreizti, R., Asteggiano, C., Bermudez, M., Córdoba, A., Szlago, M., Grosso, C., de Kremer, R. D., Vilarinho, L., D'Almeida, V., Martínez-Pardo, M., Peña-Quintana, L., Dalmau, J., Bernal, J., Briceño, I., Couce, M. L., Rodés, M., Vilaseca, M. A., Balcells, S., & Grinberg, D. (2007). Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America. Journal of human genetics, 52(4), 388-389. https://doi.org/10.1007/s10038-006-0103-4
Urreizti, Roser, et al. "Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America." Journal of human genetics vol. 52,4 (2007): 388-389. doi: https://doi.org/10.1007/s10038-006-0103-4
Urreizti R, Asteggiano C, Bermudez M, Córdoba A, Szlago M, Grosso C, de Kremer RD, Vilarinho L, D'Almeida V, Martínez-Pardo M, Peña-Quintana L, Dalmau J, Bernal J, Briceño I, Couce ML, Rodés M, Vilaseca MA, Balcells S, Grinberg D. Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America. J Hum Genet. 2007 Apr;52(4):388-389. doi: 10.1007/s10038-006-0103-4. PMID: 32033511.
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Antiallatotropins: inhibition of corpus allatum development.

Science (New York, N.Y.)

Bowers WS, Martinez-Pardo R.
PMID: 17747008
Science. 1977 Sep 30;197(4311):1369-71. doi: 10.1126/science.197.4311.1369.

Treatment of newly eclosed adult milkweed bug (Oncopeltus fasciatus) females with precocene 2 prevents secretion of juvenile hormone by inhibition of postimaginal development of the corpus allatum. Ovarian development which is dependent upon juvenile hormone is prevented or reversed,...

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Bowers WS, Martinez-Pardo R. Antiallatotropins: inhibition of corpus allatum development. Science. 1977;197(4311):1369-71doi: 10.1126/science.197.4311.1369.
Bowers, W. S., & Martinez-Pardo, R. (1977). Antiallatotropins: inhibition of corpus allatum development. Science (New York, N.Y.), 197(4311), 1369-71. https://doi.org/10.1126/science.197.4311.1369
Bowers, W S, and Martinez-Pardo, R. "Antiallatotropins: inhibition of corpus allatum development." Science (New York, N.Y.) vol. 197,4311 (1977): 1369-71. doi: https://doi.org/10.1126/science.197.4311.1369
Bowers WS, Martinez-Pardo R. Antiallatotropins: inhibition of corpus allatum development. Science. 1977 Sep 30;197(4311):1369-71. doi: 10.1126/science.197.4311.1369. PMID: 17747008.
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Enantioselective Synthesis of 5-Trifluoromethyl-2-oxazolines under Dual Silver/Organocatalysis.

The Journal of organic chemistry

Martínez-Pardo P, Blay G, Vila C, Sanz-Marco A, Muñoz MC, Pedro JR.
PMID: 30537821
J Org Chem. 2019 Jan 04;84(1):314-325. doi: 10.1021/acs.joc.8b02808. Epub 2018 Dec 21.

The first enantioselective formal [3 + 2] cycloaddition between α-isocyanoesters and trifluoromethylketones to give 5-trifluoromethyl-2-oxazolines bearing two contiguous stereogenic centers, one of them being a quaternary stereocenter substituted with a CF

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Martínez-Pardo P, Blay G, Vila C, et al. Enantioselective Synthesis of 5-Trifluoromethyl-2-oxazolines under Dual Silver/Organocatalysis. J Org Chem. 2018;84(1):314-325doi: 10.1021/acs.joc.8b02808.
Martínez-Pardo, P., Blay, G., Vila, C., Sanz-Marco, A., Muñoz, M. C., & Pedro, J. R. (2019). Enantioselective Synthesis of 5-Trifluoromethyl-2-oxazolines under Dual Silver/Organocatalysis. The Journal of organic chemistry, 84(1), 314-325. https://doi.org/10.1021/acs.joc.8b02808
Martínez-Pardo, Pablo, et al. "Enantioselective Synthesis of 5-Trifluoromethyl-2-oxazolines under Dual Silver/Organocatalysis." The Journal of organic chemistry vol. 84,1 (2019): 314-325. doi: https://doi.org/10.1021/acs.joc.8b02808
Martínez-Pardo P, Blay G, Vila C, Sanz-Marco A, Muñoz MC, Pedro JR. Enantioselective Synthesis of 5-Trifluoromethyl-2-oxazolines under Dual Silver/Organocatalysis. J Org Chem. 2019 Jan 04;84(1):314-325. doi: 10.1021/acs.joc.8b02808. Epub 2018 Dec 21. PMID: 30537821.
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Electrochemical Proton Reduction over a Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes.

ChemSusChem

Valiente A, Martínez-Pardo P, Kaur G, Johansson MJ, Martín-Matute B.
PMID: 34738723
ChemSusChem. 2021 Nov 05; doi: 10.1002/cssc.202102221. Epub 2021 Nov 05.

Selective reduction strategies based on abundant-metal catalysts are very important in the production of chemicals. In this paper, we present a method for the electrochemical semihydrogenation and semideuteration of alkynes to form Z -alkenes using a simple nickel foam...

Cite
Valiente A, Martínez-Pardo P, Kaur G, et al. Electrochemical Proton Reduction over a Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem. 2021;doi: 10.1002/cssc.202102221.
Valiente, A., Martínez-Pardo, P., Kaur, G., Johansson, M. J., & Martín-Matute, B. (2021). Electrochemical Proton Reduction over a Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem, . https://doi.org/10.1002/cssc.202102221
Valiente, Alejandro, et al. "Electrochemical Proton Reduction over a Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes." ChemSusChem vol. (2021). doi: https://doi.org/10.1002/cssc.202102221
Valiente A, Martínez-Pardo P, Kaur G, Johansson MJ, Martín-Matute B. Electrochemical Proton Reduction over a Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem. 2021 Nov 05; doi: 10.1002/cssc.202102221. Epub 2021 Nov 05. PMID: 34738723.
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Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes.

ChemSusChem

Valiente A, Martínez-Pardo P, Kaur G, Johansson MJ, Martín-Matute B.
PMID: 34738723
ChemSusChem. 2022 Jan 10;15(1):e202102221. doi: 10.1002/cssc.202102221. Epub 2021 Dec 16.

Selective reduction strategies based on abundant-metal catalysts are very important in the production of chemicals. In this paper, a method for the electrochemical semihydrogenation and semideuteration of alkynes to form Z-alkenes was developed, using a simple nickel foam as...

Cite
Valiente A, Martínez-Pardo P, Kaur G, et al. Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem. 2021;15(1):e202102221doi: 10.1002/cssc.202102221.
Valiente, A., Martínez-Pardo, P., Kaur, G., Johansson, M. J., & Martín-Matute, B. (2022). Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem, 15(1), e202102221. https://doi.org/10.1002/cssc.202102221
Valiente, Alejandro, et al. "Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes." ChemSusChem vol. 15,1 (2022): e202102221. doi: https://doi.org/10.1002/cssc.202102221
Valiente A, Martínez-Pardo P, Kaur G, Johansson MJ, Martín-Matute B. Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes. ChemSusChem. 2022 Jan 10;15(1):e202102221. doi: 10.1002/cssc.202102221. Epub 2021 Dec 16. PMID: 34738723.
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