Year |
Citation |
Score |
2023 |
Guo B, Lv J, Lu L, Hua R. Synthesis of Cyclopenta[]quinolines by Palladium-Catalyzed Cyclization of 3-Bromoindoles with Internal Alkynes via Spirocyclic Cyclopentadiene Intermediates. The Journal of Organic Chemistry. 88: 8984-8991. PMID 37339369 DOI: 10.1021/acs.joc.3c00716 |
0.585 |
|
2022 |
Lv J, Liu H, Lu L, Hua R. Copper(I)-Catalyzed Syntheses of Benzo[]fluorenes by the Cascade Reactions of 2-Alkynylbenzaldehyde -Tosylhydrazones and Aromatic Terminal Alkynes. The Journal of Organic Chemistry. PMID 36378641 DOI: 10.1021/acs.joc.2c02150 |
0.587 |
|
2021 |
Lu L, Hua R. Dual XH-π Interaction of Hexafluoroisopropanol with Arenes. Molecules (Basel, Switzerland). 26. PMID 34361719 DOI: 10.3390/molecules26154558 |
0.491 |
|
2021 |
Iqbal MA, Lu L, Mehmood H, Hua R. Biaryl Formation via Base-Promoted Direct Coupling Reactions of Arenes with Aryl Halides. Acs Omega. 6: 15981-15987. PMID 34179643 DOI: 10.1021/acsomega.1c01736 |
0.579 |
|
2020 |
Mehmood H, Iqbal MA, Lu L, Hua R. Base-Promoted Annulation of Amidoximes with Alkynes: Simple Access to 2,4-Disubstituted Imidazoles. Molecules (Basel, Switzerland). 25. PMID 32784900 DOI: 10.3390/Molecules25163621 |
0.578 |
|
2019 |
Iqbal MA, Lu L, Mehmood H, Khan DM, Hua R. Quinazolinone Synthesis through Base-Promoted SAr Reaction of -Fluorobenzamides with Amides Followed by Cyclization. Acs Omega. 4: 8207-8213. PMID 31459909 DOI: 10.1021/acsomega.9b00699 |
0.591 |
|
2018 |
Lu L, Liu H, Hua R. HNO/HFIP: A Nitrating System for Arenes with Direct Observation of π-Complex Intermediates. Organic Letters. PMID 29767980 DOI: 10.1021/Acs.Orglett.8B01028 |
0.532 |
|
2018 |
Su J, Chen Q, Lu L, Ma Y, Auyoung GHL, Hua R. Base-promoted nucleophilic fluoroarenes substitution of C F bonds Tetrahedron. 74: 303-307. DOI: 10.1016/J.Tet.2017.11.067 |
0.569 |
|
2017 |
Liu H, Lu L, Hua R. [Cu(maloNHC)]-catalyzed synthesis of 2-aryl pyrazolo[5,1-a]isoquinolines by annulation of N′-(2-((trimethylsilyl)ethynyl)benzylidene)hydrazides with terminal aromatic alkynes Tetrahedron. 73: 6428-6435. DOI: 10.1016/J.Tet.2017.09.037 |
0.56 |
|
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