المؤلفون: Vakhid A. Mamedov, Liliya V. Mustakimova, Zheng-Wang Qu, Hui Zhu, Victor V. Syakaev, Venera R. Galimullina, Leisan R. Shamsutdinova, Il’dar Kh. Rizvanov, Aidar T. Gubaidullin, Oleg G. Sinyashin, Stefan Grimme

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Pharmacology, Sociology, Plant Biology, Chemical Sciences not elsewhere classified, unique compound libraries, reactions proceed regioselectively, corrected dft calculations, 4 ‑( benzimidazol, 4 -( benzimidazol, 3 ‑( indol, 3 -( indol, methyl ­ cinnolines, excellent overall yields, 3 ‑( methyl, 3 -( methyl, yl )- 3, 3 -( aryl, yl )- quinoxalin, high yields, wide scope, starting materials, simultaneous construction, rearrangement channels, reaction mechanism, promising approach

Relation: https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707172

الاتاحة: https://doi.org/10.1021/acs.joc.3c01626.s003
https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707172

المؤلفون: Vakhid A. Mamedov, Liliya V. Mustakimova, Zheng-Wang Qu, Hui Zhu, Victor V. Syakaev, Venera R. Galimullina, Leisan R. Shamsutdinova, Il’dar Kh. Rizvanov, Aidar T. Gubaidullin, Oleg G. Sinyashin, Stefan Grimme

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Pharmacology, Sociology, Plant Biology, Chemical Sciences not elsewhere classified, unique compound libraries, reactions proceed regioselectively, corrected dft calculations, 4 ‑( benzimidazol, 4 -( benzimidazol, 3 ‑( indol, 3 -( indol, methyl ­ cinnolines, excellent overall yields, 3 ‑( methyl, 3 -( methyl, yl )- 3, 3 -( aryl, yl )- quinoxalin, high yields, wide scope, starting materials, simultaneous construction, rearrangement channels, reaction mechanism, promising approach

Relation: https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707175

الاتاحة: https://doi.org/10.1021/acs.joc.3c01626.s004
https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707175

المؤلفون: Vakhid A. Mamedov, Liliya V. Mustakimova, Zheng-Wang Qu, Hui Zhu, Victor V. Syakaev, Venera R. Galimullina, Leisan R. Shamsutdinova, Il’dar Kh. Rizvanov, Aidar T. Gubaidullin, Oleg G. Sinyashin, Stefan Grimme

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Pharmacology, Sociology, Plant Biology, Chemical Sciences not elsewhere classified, unique compound libraries, reactions proceed regioselectively, corrected dft calculations, 4 ‑( benzimidazol, 4 -( benzimidazol, 3 ‑( indol, 3 -( indol, methyl ­ cinnolines, excellent overall yields, 3 ‑( methyl, 3 -( methyl, yl )- 3, 3 -( aryl, yl )- quinoxalin, high yields, wide scope, starting materials, simultaneous construction, rearrangement channels, reaction mechanism, promising approach

Relation: https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707169

الاتاحة: https://doi.org/10.1021/acs.joc.3c01626.s002
https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707169

المؤلفون: Vakhid A. Mamedov, Liliya V. Mustakimova, Zheng-Wang Qu, Hui Zhu, Victor V. Syakaev, Venera R. Galimullina, Leisan R. Shamsutdinova, Il’dar Kh. Rizvanov, Aidar T. Gubaidullin, Oleg G. Sinyashin, Stefan Grimme

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Pharmacology, Sociology, Plant Biology, Chemical Sciences not elsewhere classified, unique compound libraries, reactions proceed regioselectively, corrected dft calculations, 4 ‑( benzimidazol, 4 -( benzimidazol, 3 ‑( indol, 3 -( indol, methyl ­ cinnolines, excellent overall yields, 3 ‑( methyl, 3 -( methyl, yl )- 3, 3 -( aryl, yl )- quinoxalin, high yields, wide scope, starting materials, simultaneous construction, rearrangement channels, reaction mechanism, promising approach

Relation: https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707166

الاتاحة: https://doi.org/10.1021/acs.joc.3c01626.s001
https://figshare.com/articles/journal_contribution/Divergent_Synthesis_of_3_Indol-2-yl_quinoxalin-2-ones_and_4_Benzimidazol-2-yl_-3-methyl_aryl_cinnolines_via_Polyphosphoric_Acid_PPA_-Mediated_Intramolecular_Rearrangements_of_3_Methyl_aryl_2-phenylhydrazono_methyl_quinoxalin-2-ones/24707166

المؤلفون: Richard R. Thompson (7553753), Madeline E. Rotella (7315112), Xin Zhou (54275), Frank R. Fronczek (568703), Osvaldo Gutierrez (1331532), Semin Lee (1493872)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Physiology, Evolutionary Biology, Ecology, Cancer, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, intermediacy, ligand, group VI alkylidynes, Dispersion-corrected DFT calculations, off-cycle decomposition products, Group VI Alkyne Metathesis Catalysts, metallacyclobutadiene, roles metal identity, alkyne metathesis, siloxide podand-supported molybdenu., species, mechanism, metallatetrahedrane

Relation: https://figshare.com/articles/journal_contribution/Impact_of_Ligands_and_Metals_on_the_Formation_of_Metallacyclic_Intermediates_and_a_Nontraditional_Mechanism_for_Group_VI_Alkyne_Metathesis_Catalysts/14763026

الاتاحة: https://doi.org/10.1021/jacs.1c01843.s001

المؤلفون: Richard R. Thompson (7553753), Madeline E. Rotella (7315112), Xin Zhou (54275), Frank R. Fronczek (568703), Osvaldo Gutierrez (1331532), Semin Lee (1493872)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Physiology, Evolutionary Biology, Ecology, Cancer, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, intermediacy, ligand, group VI alkylidynes, Dispersion-corrected DFT calculations, off-cycle decomposition products, Group VI Alkyne Metathesis Catalysts, metallacyclobutadiene, roles metal identity, alkyne metathesis, siloxide podand-supported molybdenu., species, mechanism, metallatetrahedrane

Relation: https://figshare.com/articles/dataset/Impact_of_Ligands_and_Metals_on_the_Formation_of_Metallacyclic_Intermediates_and_a_Nontraditional_Mechanism_for_Group_VI_Alkyne_Metathesis_Catalysts/14763029

الاتاحة: https://doi.org/10.1021/jacs.1c01843.s002