A HUN-REN Magyar Kutatási Hálózat intézményi tárolója

A HUN-REN Magyar Kutatási Hálózat a magyar tudományos élet alappillérét jelentő kutatási hálózat. A hálózat tizenegy kutatóközpontjának, hét kutatóintézetének, továbbá egyetemeken és más közintézményekben működő 116 támogatott kutatócsoportjának kutatói a matematikai és természettudományok, az élettudományok, illetve a bölcsészet- és társadalomtudományok legváltozatosabb területein végeznek alap- és alkalmazott kutatásokat.
Featured Dataverses

In order to use this feature you must have at least one published or linked dataverse.

Publish Dataverse

Are you sure you want to publish your dataverse? Once you do so it must remain published.

Publish Dataverse

This dataverse cannot be published because the dataverse it is in has not been published.

Delete Dataverse

Are you sure you want to delete your dataverse? You cannot undelete this dataverse.

Advanced Search

651 to 660 of 36,923 Results
Environmental Toxicology Projects(HUN-REN Balaton Limnological Research Institute)
Jan 29, 2026Research Projects (BLRI)
Microbial Ecology Research Group(HUN-REN Centre for Ecological Research)
Jan 26, 2026Institute of Aquatic Ecology, Centre for Ecological Research
Dataverse for the Microbial Ecology Research Group = A Mikrobiális Ökológiai Kutatócsoport adategyüttese
Supporting information for Selective Synthesis of Tetrahydroisoquinoline and Piperidine Scaffolds by Oxidative Ring Opening/Ring Closing Protocols of Substituted Indenes and Cyclopentenes
Jan 26, 2026 - Artificial Transporters Research Group
Nonn, Melinda, 2026, "Supporting information for Selective Synthesis of Tetrahydroisoquinoline and Piperidine Scaffolds by Oxidative Ring Opening/Ring Closing Protocols of Substituted Indenes and Cyclopentenes", https://hdl.handle.net/21.15109/ARP/Q8W6OO, ARP, V1
Synthesis of tetrahydroisoquinoline and Piperidine Scaffolds by Oxidative Ring Opening/Ring Closing Protocols of Substituted Indenes and Cyclopentenes were demonstrated in this article. The synthesis was based by using some elementary organic chemistry reactions. The products wer...
sup.inf.Chemopen.2025.14.e202400475.pdf
Jan 26, 2026 - Supporting information for Selective Synthesis of Tetrahydroisoquinoline and Piperidine Scaffolds by Oxidative Ring Opening/Ring Closing Protocols of Substituted Indenes and Cyclopentenes
Adobe PDF - 1.1 MB - MD5: b71c70ef7e6b25f6f2b9a7e597082921
Supplementary information of Selective Synthesis of Tetrahydroisoquinoline and Piperidine Scaffolds by Oxidative Ring Opening/Ring Closing Protocols of Substituted Indenes and Cyclopentenes paper
Artificial Transporters Research Group(HUN-REN Research Centre for Natural Sciences)
Jan 15, 2026Institute of Materials and Environmental Chemistry
CH3O_radical.tar.gz
Jan 10, 2026 - Exe.py: Ab initio fine structure parameters for trigonal defect qubits within the E⊗e Jahn-Teller case
Gzip Archive - 898.3 KB - MD5: 554e8d22b5a33427616a82132c991858
Group_IV_vacancies.tar.gz
Jan 10, 2026 - Exe.py: Ab initio fine structure parameters for trigonal defect qubits within the E⊗e Jahn-Teller case
Gzip Archive - 205.9 MB - MD5: bb89258bc809ad366a86421caba2b3e7
Jahn-Teller_parameters.csv
Jan 10, 2026 - Exe.py: Ab initio fine structure parameters for trigonal defect qubits within the E⊗e Jahn-Teller case
Comma Separated Values - 534 B - MD5: 0bb1fa646b4fcc44b4894f16060e6877
N3V0_C3v_to_C1h_min.csv
Jan 10, 2026 - Exe.py: Ab initio fine structure parameters for trigonal defect qubits within the E⊗e Jahn-Teller case
Comma Separated Values - 1.0 KB - MD5: 79f7ffc2899dc1c486ec9ce3cb094424
N3V0_C3v_to_C1h_sadd.csv
Jan 10, 2026 - Exe.py: Ab initio fine structure parameters for trigonal defect qubits within the E⊗e Jahn-Teller case
Comma Separated Values - 1.0 KB - MD5: 5cd9232350662854465c321ed827221b
Add Data

Sign up or log in to create a dataverse or add a dataset.

Sign Up Log In
Share Dataverse

Share this dataverse on your favorite social media networks.

Link Dataverse
Reset Modifications

Are you sure you want to reset the selected metadata fields? If you do this, any customizations (hidden, required, optional) you have done will no longer appear.