OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Ligand-controlled iridium-catalyzed semihydrogenation of alkynes with ethanol: highly stereoselective synthesis of E- and Z-alkenes
Jinfei Yang, Chengniu Wang, Yufeng Sun, et al.
Chemical Communications (2019) Vol. 55, Iss. 13, pp. 1903-1906
Closed Access | Times Cited: 60

Showing 26-50 of 60 citing articles:

Substrate-Controlled Cu(OAc)2-Catalyzed Stereoselective Semi-Reduction of Alkynes with MeOH as the Hydrogen Source
Jiuzhong Huang, Xiaoning Li, Hui‐Ling Wen, et al.
ACS Omega (2021) Vol. 6, Iss. 17, pp. 11740-11749
Open Access | Times Cited: 17

Controlling hydrogen transfer dynamics in adaptive semihydrogenation of alkynes: Unveiling and directing outer- vs. inner-sphere mechanisms
Vishal Chugh, Jiajun Wu, Markus Leutzsch, et al.
Chem Catalysis (2024) Vol. 4, Iss. 9, pp. 101078-101078
Closed Access | Times Cited: 2

Two resveratrol analogs, pinosylvin and 4,4′-dihydroxystilbene, improve oligoasthenospermia in a mouse model by attenuating oxidative stress via the Nrf2-ARE pathway
Cheng-niu Wang, Mengmeng Sang, Shengnan Gong, et al.
Bioorganic Chemistry (2020) Vol. 104, pp. 104295-104295
Closed Access | Times Cited: 18

Manganese-catalyzed transfer semihydrogenation of internal alkynes to E-alkenes with iPrOH as hydrogen source
Antonio Torres-Calis, Juventino J. Garcı́a
Catalysis Science & Technology (2022) Vol. 12, Iss. 9, pp. 3004-3015
Closed Access | Times Cited: 11

Structural snapshots of an Al–Cu bond-mediated transformation of terminal acetylenes
Han‐Ying Liu, Samuel E. Neale, Michael S. Hill, et al.
Chemical Science (2023) Vol. 14, Iss. 11, pp. 2866-2876
Open Access | Times Cited: 6

H2O as the Hydrogen Donor: Stereo-Selective Synthesis of E- and Z-Alkenes by Palladium-Catalyzed Semihydrogenation of Alkynes
Jianwu Shi, Taowen Ye, Jin Dong, et al.
ACS Omega (2023) Vol. 8, Iss. 12, pp. 11492-11502
Open Access | Times Cited: 6

Room temperature Z-selective hydrogenation of alkynes by hemilabile and non-innocent (NNN)Co(ii) catalysts
Dipesh M. Sharma, Chandrakant Gouda, Rajesh G. Gonnade, et al.
Catalysis Science & Technology (2022) Vol. 12, Iss. 6, pp. 1843-1849
Closed Access | Times Cited: 9

CuCl2-catalyzed highly stereoselective and chemoselective reduction of alkynyl amides into α,β-unsaturated amides using silanes as hydrogen donors
Lingfei Duan, Kai Jiang, Hua Zhu, et al.
Organic & Biomolecular Chemistry (2020) Vol. 19, Iss. 2, pp. 365-369
Closed Access | Times Cited: 13

Ruthenium(ii)-catalyzed reductive N–O bond cleavage ofN-OR (R = H, alkyl, or acyl) substituted amides and sulfonamides
Tingjie You, Maosheng Zhang, Jianhui Chen, et al.
Organic Chemistry Frontiers (2020) Vol. 8, Iss. 1, pp. 112-119
Closed Access | Times Cited: 12

Catalytic, Transition-Metal-Free Semireduction of Propiolamide Derivatives: Scope and Mechanistic Investigation
R. Justin Grams, Christopher J. Garcia, Connor Szwetkowski, et al.
Organic Letters (2020) Vol. 22, Iss. 17, pp. 7013-7018
Open Access | Times Cited: 11

Membrane‐Free Selective Semi‐Hydrogenation of Alkynes Over an In Situ Formed Copper Nanoparticle Electrode
Pengyu Guo, Yousen Xu, Hao Bin Wu, et al.
Small (2024) Vol. 20, Iss. 33
Closed Access | Times Cited: 1

Modulating the Aggregation States of a Pd6L4 Cage for Selectivity Flipping during the Stereo‐Divergent Semi‐Hydrogenation of Alkynes
Wei Zhong, Xu Jing, Zhao Song, et al.
Angewandte Chemie International Edition (2024)
Closed Access | Times Cited: 1

Catalytic and mechanistic studies of a highly active and E-selective Co(ii) PNNH pincer catalyst system for transfer-semihydrogenation of internal alkynes
David L. Decker, Zhihong Wei, Jabor Rabeah, et al.
Inorganic Chemistry Frontiers (2022) Vol. 9, Iss. 4, pp. 761-770
Closed Access | Times Cited: 6

Palladium-Catalyzed Semihydrogenation of Alkynes with EtOH: Highly Stereoselective Synthesis of E- and Z-Alkenes
Chengniu Wang, Jin Dong, Dawei Xu, et al.
Synthesis (2022) Vol. 54, Iss. 11, pp. 2687-2695
Closed Access | Times Cited: 6

Organocatalytic Trans Semireduction of Primary and Secondary Propiolamides: Substrate Scope and Mechanistic Studies
R. Justin Grams, Monsurat M. Lawal, Connor Szwetkowski, et al.
Advanced Synthesis & Catalysis (2021) Vol. 364, Iss. 1, pp. 172-178
Closed Access | Times Cited: 6

Protocol for (E)-selective semihydrogenation of alkynes using iridium-based catalyst
Rafał Kusy, Karol Grela
STAR Protocols (2023) Vol. 4, Iss. 4, pp. 102579-102579
Open Access | Times Cited: 2

E-Selective semi-hydrogenation of alkynes via a sulfur-radical mediation over cyclodextrin-modified nickel nanocatalyst
Yatao Su, Xiu Wang, Qianwen Lin, et al.
Catalysis Science & Technology (2023) Vol. 13, Iss. 6, pp. 1718-1724
Closed Access | Times Cited: 2

A ligand-free in situ-generated cobalt nanoparticle catalyst for (Z)-selective transfer semihydrogenation of alkynes
Shunbin Yang, Dengju Zhang, Weiguo Zuo, et al.
New Journal of Chemistry (2023) Vol. 47, Iss. 40, pp. 18634-18639
Closed Access | Times Cited: 2

Selective reduction of alkynes to alkenes with hydrogen or formic acid catalyzed by cis,mer-[IrH2Cl(mtppms)3]
György Hankó, Richárd Márton, Antal Udvardy, et al.
Inorganica Chimica Acta (2021) Vol. 522, pp. 120359-120359
Open Access | Times Cited: 5

Bidentate Ru(II)‐NC Complexes as Catalysts for Transfer Hydrogenation of Ketones with Ethanol
Yufei Li, Shuang Lian, Jiku Wang, et al.
Asian Journal of Organic Chemistry (2024) Vol. 13, Iss. 3
Closed Access

BioLindlar Catalyst: Ene‐Reductase‐Promoted Selective Bioreduction of Cyanoalkynes to Give (Z)‐Cyanoalkenes
Jorge González-Rodríguez, Sergio González‐Granda, Hirdesh Kumar, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 39
Open Access

BioLindlar Catalyst: Ene‐Reductase‐Promoted Selective Bioreduction of Cyanoalkynes to Give (Z)‐Cyanoalkenes
Jorge González-Rodríguez, Sergio González‐Granda, Hirdesh Kumar, et al.
Angewandte Chemie International Edition (2024)
Open Access

Visible-Light-Driven (NSNO)Nickel complex catalyzed (Z)-Selective semi-hydrogenation of alkynes
Nuo Zhang, Yongbo Zhou, Fei Chen, et al.
Fuel (2024) Vol. 383, pp. 133844-133844
Closed Access

Scroll to top