2021
DOI: 10.1016/s1872-2067(20)63773-1
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Highly selective catalysts for the hydrogenation of alkynols: A review

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Cited by 41 publications
(21 citation statements)
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“…The semi‐hydrogenation of alkynols to cis ‐alkenols is known to depend on either electronic or steric effects exerted by the heterogeneous catalyst [11b] . In this context, we found that the hydrogenation reaction of 3‐hexyn‐1‐ol to cis ‐3‐hexen‐1‐ol is much more sensitive to the structure of the catalysts, compared to the reaction of 2‐butyne‐1,4‐diol to cis ‐2‐butene‐1,4‐diol ( i. e .…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The semi‐hydrogenation of alkynols to cis ‐alkenols is known to depend on either electronic or steric effects exerted by the heterogeneous catalyst [11b] . In this context, we found that the hydrogenation reaction of 3‐hexyn‐1‐ol to cis ‐3‐hexen‐1‐ol is much more sensitive to the structure of the catalysts, compared to the reaction of 2‐butyne‐1,4‐diol to cis ‐2‐butene‐1,4‐diol ( i. e .…”
Section: Resultsmentioning
confidence: 99%
“…−1.02 eV for propene adsorption on the 111 surface of Pd), [11a] and the formation of a Pd‐hydride phase which fosters over‐hydrogenation to the corresponding saturated compound. In fact, DRIFT spectroscopic studies conducted on alkynol hydrogenation reactions, [7k,11b] along with DFT‐based calculations carried out on a Pd 9 (H) 2 model cluster surface confirmed a much faster carbon‐carbon triple than double bond hydrogenation, with an energy gap of approximately 50 kJ mol −1 [11c] . Hence the formation of Pd‐alloys with other metals such as Cu ( i. e .…”
Section: Introductionmentioning
confidence: 98%
“…The semi-hydrogenation of alkynols to enols also has attracted considerable attention in recent years. 44,62 Surprisingly, Pd 0.43 Co 1 /m-NC also exhibited excellent catalytic performance with high selectivity for the semi-hydrogenation of alkynols to enol products (Table 2, entries 1-8). Thus, the obtained Pd 0.43 Co 1 /m-NC catalyst exhibits excellent general applicability for the semi-hydrogenation of alkyl compounds.…”
Section: Paper Dalton Transactionsmentioning
confidence: 99%
“…However, the ability of aromatic molecules with reducible functional groups (such as C=C, NO 2 , C=O, etc.) to be activated or reduced is different [ 5 , 6 ]. How to accurately reduce the appointed groups is still a challenge.…”
Section: Introductionmentioning
confidence: 99%