1969
DOI: 10.1021/jo01263a122
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Homogeneous catalytic hydrogenation of unsaturated organic compounds

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Cited by 59 publications
(23 citation statements)
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“…Further, use of microwave irradiation on solid-supported reactions has enhanced the impact of the latter as the high heating efficiency of microwave results in remarkable rate enhancement, higher yields, greater selectivity, and ease of manipulation of such reactions [3]. In addition, the limitation of the microwave-assisted reactions in solvents enforcing development of high pressure and special sealed vessels are circumvented by this solid-support strategy [4], which enables organic reactions such as oxidation, hydrogenation, etc., to occur rapidly at atmospheric pressure and to upscale the reaction on a preparative scale.A lot of hydrogenation protocols are available for the selective hydrogenation of C=C bonds of unsaturated esters which either require a special apparatus and H 2 gas (potentially explosive) [5] …”
mentioning
confidence: 99%
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“…Further, use of microwave irradiation on solid-supported reactions has enhanced the impact of the latter as the high heating efficiency of microwave results in remarkable rate enhancement, higher yields, greater selectivity, and ease of manipulation of such reactions [3]. In addition, the limitation of the microwave-assisted reactions in solvents enforcing development of high pressure and special sealed vessels are circumvented by this solid-support strategy [4], which enables organic reactions such as oxidation, hydrogenation, etc., to occur rapidly at atmospheric pressure and to upscale the reaction on a preparative scale.A lot of hydrogenation protocols are available for the selective hydrogenation of C=C bonds of unsaturated esters which either require a special apparatus and H 2 gas (potentially explosive) [5] …”
mentioning
confidence: 99%
“…Ethyl 3-Phenylpropanoate (1b) [5] [6m] [10]: Liquid. 1 H-NMR (CDCl 3 , 300 MHz): 7.23 -7.17 (m, 3 H); 7.14 (d, J = 6.86, 2 H); 4.08 (q, J = 6.86, 2 H); 2.90 (t, J = 7.67, 2 H); 2.57 (t, J = 7.67, 2 H); 1.17 (t, J = 6.86, 3 H).…”
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confidence: 99%
“…(Young et al, 1947;Brown & Brown, 1962;Harmon et al, 1969;Ohkuma et al, 1995;Lu et al, 2008) In this context, the preparation and stabilisation of metal NPs becomes a suitable alternative for the classical homogeneous and heterogeneous systems. (Crooks et al, 2001;Thomas et al, 2003;Astruc et al, 2005;Yan et al, 2010) Particularly, metal NPs prepared in ILs proved to be an outstanding recyclable catalytic-phase for the hydrogenation of different substrates exhibiting high catalytic activities.…”
Section: Hydrogenation Reactions Catalysed By Pd-nps In Ilsmentioning
confidence: 99%
“…The same recipe was applied for the synthesis of P -D labeled 7. 1H NMR of P -D labeled 7 (acetone-d6): 3.21 and 2.79 (two m, 4H, -CH2CHDS-), 2.12 (s, 3H,…”
Section: -Methylthio-2-oxobutyric Acid (7)mentioning
confidence: 99%