OpenAlex Citation Counts

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:

Metal Nanoparticles Catalyzed C–C Bond Formation via C–H Activation
Federica Valentini, Giulia Brufani, Loredana Latterini, et al.
ACS symposium series (2020), pp. 513-543
Closed Access | Times Cited: 15

Showing 15 citing articles:

Copper nanocatalysts applied in coupling reactions: a mechanistic insight
Marc Camats, Daniel Plá, Montserrat Gómez
Nanoscale (2021) Vol. 13, Iss. 45, pp. 18817-18838
Open Access | Times Cited: 33

Recent progress in applications of cobalt catalysts in organic reactions
Mohammad Mostafa Tohidi, Behnaz Paymard, Salomon Ramiro Vasquez-García, et al.
Tetrahedron (2023) Vol. 136, pp. 133352-133352
Closed Access | Times Cited: 12

Valorisation of urban waste to access low-cost heterogeneous palladium catalysts for cross-coupling reactions in biomass-derived γ-valerolactone
Federica Valentini, Francesco Ferlin, Simone Lilli, et al.
Green Chemistry (2021) Vol. 23, Iss. 16, pp. 5887-5895
Closed Access | Times Cited: 29

Aerobic waste-minimized Pd-catalysed C–H alkenylation in GVL using a tube-in-tube heterogeneous flow reactor
Francesco Ferlin, Ioannis Anastasiou, Luigi Carpisassi, et al.
Green Chemistry (2021) Vol. 23, Iss. 17, pp. 6576-6582
Closed Access | Times Cited: 23

Tailor-Made POLITAG-Pd⁰ Catalyst for the Low-Loading Mizoroki–Heck Reaction in γ-Valerolactone as a Safe Reaction Medium
Federica Valentini, Luigi Carpisassi, Adrien Comès, et al.
ACS Sustainable Chemistry & Engineering (2022) Vol. 10, Iss. 37, pp. 12386-12393
Open Access | Times Cited: 17

C(sp³)−H Arylation Promoted by a Heterogeneous Palladium‐N‐Heterocyclic Carbene Complex in Batch and Continuous Flow
Francesco Ferlin, Ioannis Anastasiou, Nihad Salameh, et al.
ChemSusChem (2022) Vol. 15, Iss. 6
Open Access | Times Cited: 16

A Waste‐Minimized Approach to Cassar‐Heck Reaction Based on POLITAG‐Pd ⁰ Heterogeneous Catalyst and Recoverable Acetonitrile Azeotrope
Federica Valentini, Francesco Ferlin, Elena Tomarelli, et al.
ChemSusChem (2021) Vol. 14, Iss. 16, pp. 3359-3366
Open Access | Times Cited: 18

Classic vs. C–H functionalization strategies in the synthesis of APIs: a sustainability comparison
Francesco Ferlin, Giulia Brufani, Gabriele Rossini, et al.
Green Chemistry (2023) Vol. 25, Iss. 20, pp. 7916-7933
Open Access | Times Cited: 7

Gold nanoparticle decorated post-synthesis modified UiO-66-NH2 for A3-coupling preparation of propargyl amines
Leila Mohammadi, Reza Taghavi, Mojtaba Hosseinifard, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 6

Metal Nanoparticles as Sustainable Tools for C–N Bond Formation via C–H Activation
Federica Valentini, Oriana Piermatti, Luigi Vaccaro
Molecules (2021) Vol. 26, Iss. 13, pp. 4106-4106
Open Access | Times Cited: 12

Bringing Selectivity in H/D Exchange Reactions Catalyzed by Metal Nanoparticles through Modulation of the Metal and the Ligand Shell
Francisco Martinez-Espinar, Antoni Salóm-Català, Emma Bresó-Femenia, et al.
Inorganic Chemistry (2023) Vol. 62, Iss. 11, pp. 4570-4580
Open Access | Times Cited: 4

Magnetically recoverable nickel-palladium alloy nanocatalysts for direct C–H arylation reactions
Yunus Zozik, Melike Sevim, Ferruh Lafzi, et al.
Dalton Transactions (2021) Vol. 50, Iss. 47, pp. 17515-17523
Closed Access | Times Cited: 7

Metal and Metal Oxide Nanoparticles Catalyzed C–H Activation for C–O and C–X (X = Halogen, B, P, S, Se) Bond Formation
Federica Valentini, Oriana Piermatti, Luigi Vaccaro
Catalysts (2022) Vol. 13, Iss. 1, pp. 16-16
Open Access | Times Cited: 4

Understanding Cu(ii)-based systems for C(sp³)–H bond functionalization: insights into the synthesis of aza-heterocycles
Marc Camats, Isabelle Favier, Sonia Mallet‐Ladeira, et al.
Organic & Biomolecular Chemistry (2021) Vol. 20, Iss. 1, pp. 219-227
Open Access | Times Cited: 5

Palladium Nanoparticles in CH Functionalization Reactions
Chander Shekhar, Dakoju Ravi Kishore, Gedu Satyanarayana
Handbook of CH‐Functionalization (2022), pp. 1-36
Closed Access

Page 1

Cookie	Duration	Description
cookielawinfo-checkbox-advertisement	1 year	Set by the GDPR Cookie Consent plugin, this cookie is used to record the user consent for the cookies in the "Advertisement" category .
cookielawinfo-checkbox-analytics	1 year	Set by the GDPR Cookie Consent plugin, this cookie is used to record the user consent for the cookies in the "Analytics" category .
cookielawinfo-checkbox-functional	1 year	The cookie is set by the GDPR Cookie Consent plugin to record the user consent for the cookies in the category "Functional".
cookielawinfo-checkbox-necessary	1 year	Set by the GDPR Cookie Consent plugin, this cookie is used to record the user consent for the cookies in the "Necessary" category .
cookielawinfo-checkbox-others	1 year	Set by the GDPR Cookie Consent plugin, this cookie is used to store the user consent for cookies in the category "Others".
cookielawinfo-checkbox-performance	1 year	Set by the GDPR Cookie Consent plugin, this cookie is used to store the user consent for cookies in the category "Performance".
CookieLawInfoConsent	1 year	Records the default button state of the corresponding category & the status of CCPA. It works only in coordination with the primary cookie.
PHPSESSID	session	This cookie is native to PHP applications. The cookie is used to store and identify a users' unique session ID for the purpose of managing user session on the website. The cookie is a session cookies and is deleted when all the browser windows are closed.

Requested Article:

Showing 15 citing articles:

Your Privacy