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Sustainable Hydrogenation of Vinyl Derivatives Using Pd/C Catalysts. / Mironenko, Roman M. ; Saybulina, Elina R. ; Stepanova, Liudmila N. ; Gulyaeva, Tatiana I. ; Trenikhin , Mikhail V. ; Rodygin, Konstantin S. ; Ananikov, Valentine P. .

In: Catalysts, Vol. 11, No. 2, 179, 02.2021.

Research output: Contribution to journalArticlepeer-review

Harvard

Mironenko, RM, Saybulina, ER, Stepanova, LN, Gulyaeva, TI, Trenikhin , MV, Rodygin, KS & Ananikov, VP 2021, 'Sustainable Hydrogenation of Vinyl Derivatives Using Pd/C Catalysts', Catalysts, vol. 11, no. 2, 179. https://doi.org/10.3390/catal11020179

APA

Mironenko, R. M., Saybulina, E. R., Stepanova, L. N., Gulyaeva, T. I., Trenikhin , M. V., Rodygin, K. S., & Ananikov, V. P. (2021). Sustainable Hydrogenation of Vinyl Derivatives Using Pd/C Catalysts. Catalysts, 11(2), [179]. https://doi.org/10.3390/catal11020179

Vancouver

Mironenko RM, Saybulina ER, Stepanova LN, Gulyaeva TI, Trenikhin MV, Rodygin KS et al. Sustainable Hydrogenation of Vinyl Derivatives Using Pd/C Catalysts. Catalysts. 2021 Feb;11(2). 179. https://doi.org/10.3390/catal11020179

Author

Mironenko, Roman M. ; Saybulina, Elina R. ; Stepanova, Liudmila N. ; Gulyaeva, Tatiana I. ; Trenikhin , Mikhail V. ; Rodygin, Konstantin S. ; Ananikov, Valentine P. . / Sustainable Hydrogenation of Vinyl Derivatives Using Pd/C Catalysts. In: Catalysts. 2021 ; Vol. 11, No. 2.

BibTeX

@article{1cfab125c4a549c89fdd77e6390b9846,
title = "Sustainable Hydrogenation of Vinyl Derivatives Using Pd/C Catalysts",
abstract = "The hydrogenation of unsaturated double bonds with molecular hydrogen is an efficient atom-economic approach to the production of a wide range of fine chemicals. In contrast to a number of reducing reagents typically involved in organic synthesis, hydrogenation with H2 is much more sustainable since it does not produce wastes (i.e., reducing reagent residues). However, its full sustainable potential may be achieved only in the case of easily separable catalysts and high reaction selectivity. In this work, various Pd/C catalysts were used for the liquid-phase hydrogenation of O-, S-, and N-vinyl derivatives with molecular hydrogen under mild reaction conditions (room temperature, pressure of 1 MPa). Complete conversion and high hydrogenation selectivity (>99%) were achieved by adjusting the type of Pd/C catalyst. Thus, the proposed procedure can be used as a sustainable method for vinyl group transformation by hydrogenation reactions. The discovery of the stability of active vinyl functional groups conjugated with heteroatoms (O, S, and N) under hydrogenation conditions over Pd/C catalysts opens the way for many useful transformations.",
keywords = "molecular hydrogen, hydrogenation, Pd/C catalysts, calcium carbide, acetylene, vinyl group, Molecular hydrogen, Calcium carbide, Vinyl group, Hydrogenation, Acetylene",
author = "Mironenko, {Roman M.} and Saybulina, {Elina R.} and Stepanova, {Liudmila N.} and Gulyaeva, {Tatiana I.} and Trenikhin, {Mikhail V.} and Rodygin, {Konstantin S.} and Ananikov, {Valentine P.}",
note = "Publisher Copyright: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2021",
month = feb,
doi = "10.3390/catal11020179",
language = "English",
volume = "11",
journal = "Catalysts",
issn = "2073-4344",
publisher = "MDPI AG",
number = "2",

}

RIS

TY - JOUR

T1 - Sustainable Hydrogenation of Vinyl Derivatives Using Pd/C Catalysts

AU - Mironenko, Roman M.

AU - Saybulina, Elina R.

AU - Stepanova, Liudmila N.

AU - Gulyaeva, Tatiana I.

AU - Trenikhin , Mikhail V.

AU - Rodygin, Konstantin S.

AU - Ananikov, Valentine P.

N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

PY - 2021/2

Y1 - 2021/2

N2 - The hydrogenation of unsaturated double bonds with molecular hydrogen is an efficient atom-economic approach to the production of a wide range of fine chemicals. In contrast to a number of reducing reagents typically involved in organic synthesis, hydrogenation with H2 is much more sustainable since it does not produce wastes (i.e., reducing reagent residues). However, its full sustainable potential may be achieved only in the case of easily separable catalysts and high reaction selectivity. In this work, various Pd/C catalysts were used for the liquid-phase hydrogenation of O-, S-, and N-vinyl derivatives with molecular hydrogen under mild reaction conditions (room temperature, pressure of 1 MPa). Complete conversion and high hydrogenation selectivity (>99%) were achieved by adjusting the type of Pd/C catalyst. Thus, the proposed procedure can be used as a sustainable method for vinyl group transformation by hydrogenation reactions. The discovery of the stability of active vinyl functional groups conjugated with heteroatoms (O, S, and N) under hydrogenation conditions over Pd/C catalysts opens the way for many useful transformations.

AB - The hydrogenation of unsaturated double bonds with molecular hydrogen is an efficient atom-economic approach to the production of a wide range of fine chemicals. In contrast to a number of reducing reagents typically involved in organic synthesis, hydrogenation with H2 is much more sustainable since it does not produce wastes (i.e., reducing reagent residues). However, its full sustainable potential may be achieved only in the case of easily separable catalysts and high reaction selectivity. In this work, various Pd/C catalysts were used for the liquid-phase hydrogenation of O-, S-, and N-vinyl derivatives with molecular hydrogen under mild reaction conditions (room temperature, pressure of 1 MPa). Complete conversion and high hydrogenation selectivity (>99%) were achieved by adjusting the type of Pd/C catalyst. Thus, the proposed procedure can be used as a sustainable method for vinyl group transformation by hydrogenation reactions. The discovery of the stability of active vinyl functional groups conjugated with heteroatoms (O, S, and N) under hydrogenation conditions over Pd/C catalysts opens the way for many useful transformations.

KW - molecular hydrogen

KW - hydrogenation

KW - Pd/C catalysts

KW - calcium carbide

KW - acetylene

KW - vinyl group

KW - Molecular hydrogen

KW - Calcium carbide

KW - Vinyl group

KW - Hydrogenation

KW - Acetylene

UR - https://www.mdpi.com/2073-4344/11/2/179/html

UR - http://www.scopus.com/inward/record.url?scp=85099850888&partnerID=8YFLogxK

U2 - 10.3390/catal11020179

DO - 10.3390/catal11020179

M3 - Article

VL - 11

JO - Catalysts

JF - Catalysts

SN - 2073-4344

IS - 2

M1 - 179

ER -

ID: 73271321