Year |
Citation |
Score |
2023 |
Liao X, Zhou H, Chen X, Xu J. Isothiourea-Catalyzed Acylative Desymmetrization of Silicon-Centered Bisphenols. Organic Letters. 25: 3099-3103. PMID 37129310 DOI: 10.1021/acs.orglett.3c00946 |
0.346 |
|
2022 |
Chen T, Gong F, Nagaraju S, Liu J, Yang S, Chen X, Fang X. Oxa-Nazarov Cyclization-Michael Addition Sequence for the Rapid Construction of Dihydrofuranones. Organic Letters. 24: 8837-8842. PMID 36417711 DOI: 10.1021/acs.orglett.2c03601 |
0.689 |
|
2022 |
Luo C, Xu X, Xu J, Chen X. Oxidant free synthesis of α-pyrones an NHC-catalyzed [3 + 3] annulation of bromoenals with 2-chloro-1,3-diketones. Organic & Biomolecular Chemistry. PMID 36398963 DOI: 10.1039/d2ob01859d |
0.508 |
|
2022 |
Liu H, Zhou H, Chen X, Xu J. N-Heterocyclic Carbene-Catalyzed Desymmetrization of Siladials To Access Silicon-Stereogenic Organosilanes. The Journal of Organic Chemistry. PMID 36395464 DOI: 10.1021/acs.joc.2c02184 |
0.34 |
|
2020 |
Chen X, Wang H, Jin Z, Chi YR. N
‐Heterocyclic
Carbene Organocatalysis: Activation Modes and Typical Reactive Intermediates Chinese Journal of Chemistry. 38: 1167-1202. DOI: 10.1002/Cjoc.202000107 |
0.358 |
|
2019 |
Wang H, Wang Y, Chen X, Mou C, Yu S, Chai H, Jin Z, Chi YR. Chiral Nitroarenes as Enantioselective Single-Electron-Transfer Oxidants for Carbene-Catalyzed Radical Reactions. Organic Letters. PMID 31478384 DOI: 10.1021/acs.orglett.9b02736 |
0.579 |
|
2019 |
Huang R, Chen X, Mou C, Luo G, Li Y, Li X, Xue W, Jin Z, Chi YR. Carbene-Catalyzed α-Carbon Amination of Chloroaldehydes for Enantioselective Access to Dihydroquinoxaline Derivatives. Organic Letters. PMID 31117715 DOI: 10.1021/acs.orglett.9b01520 |
0.641 |
|
2019 |
Liu Y, Chen Q, Mou C, Pan L, Duan X, Chen X, Chen H, Zhao Y, Lu Y, Jin Z, Chi YR. Catalytic asymmetric acetalization of carboxylic acids for access to chiral phthalidyl ester prodrugs. Nature Communications. 10: 1675. PMID 30975988 DOI: 10.1038/s41467-019-09445-x |
0.605 |
|
2017 |
Wang H, Chen X, Li Y, Wang J, Wu S, Xue W, Yang S, Chi YR. Addition of N-Heterocyclic Carbene Catalyst to Aryl Esters Induces Remote C-Si Bond Activation and Benzylic Carbon Functionalization. Organic Letters. PMID 29286252 DOI: 10.1021/acs.orglett.7b03544 |
0.574 |
|
2017 |
Chen X, Yang S, Song BA, Chi YR. Corrigendum: Functionalization of Benzylic C(sp(3) )-H Bonds of Heteroaryl Aldehydes through N-Heterocyclic Carbene Organocatalysis. Angewandte Chemie (International Ed. in English). 56: 14342. PMID 29115048 DOI: 10.1002/anie.201710032 |
0.536 |
|
2017 |
Chen X, Song R, Liu Y, Ooi CY, Jin Z, Zhu T, Wang H, Hao L, Chi YR. Carbene and Acid Cooperative Catalytic Reactions of Aldehydes and o-Hydroxybenzhydryl Amines for Highly Enantioselective Access to Dihydrocoumarins. Organic Letters. PMID 29068212 DOI: 10.1021/Acs.Orglett.7B02883 |
0.76 |
|
2017 |
Chen X, Wang H, Doitomi K, Ooi CY, Zheng P, Liu W, Guo H, Yang S, Song BA, Hirao H, Chi YR. A reaction mode of carbene-catalysed aryl aldehyde activation and induced phenol OH functionalization. Nature Communications. 8: 15598. PMID 28541276 DOI: 10.1038/ncomms15598 |
0.649 |
|
2016 |
Chen X, Fong JZ, Xu J, Mou C, Lu Y, Yang S, Song BA, Chi YR. Carbene-Catalyzed Dynamic Kinetic Resolution of Carboxylic Esters. Journal of the American Chemical Society. PMID 27219078 DOI: 10.1021/jacs.6b00406 |
0.688 |
|
2015 |
Xu J, Chen X, Wang M, Zheng P, Song BA, Chi YR. Aminomethylation of enals through carbene and acid cooperative catalysis: concise access to β(2)-amino acids. Angewandte Chemie (International Ed. in English). 54: 5161-5. PMID 25735973 DOI: 10.1002/anie.201412132 |
0.591 |
|
2014 |
Hao L, Chen X, Chen S, Jiang K, Torres J, Chi YR. Access to pyridines via DMAP-catalyzed activation of α-chloro acetic ester to react with unsaturated imines Org. Chem. Front.. 1: 148-150. DOI: 10.1039/C3QO00045A |
0.45 |
|
2013 |
Chen X, Yang S, Song BA, Chi YR. Functionalization of benzylic C(sp(3))-H bonds of heteroaryl aldehydes through N-heterocyclic carbene organocatalysis. Angewandte Chemie (International Ed. in English). 52: 11134-7. PMID 24038663 DOI: 10.1002/anie.201305861 |
0.647 |
|
2013 |
Mo J, Yang R, Chen X, Tiwari B, Chi YR. Direct α-functionalization of simple aldehydes via oxidative N-heterocyclic carbene catalysis. Organic Letters. 15: 50-3. PMID 23249417 DOI: 10.1021/ol303035r |
0.782 |
|
2013 |
Chen X, Fang X, Chi YR. cis-Enals in N-heterocyclic carbene-catalyzed reactions: distinct stereoselectivity and reactivity Chemical Science. 4: 2613. DOI: 10.1039/C3Sc50666E |
0.71 |
|
2013 |
Leong WWY, Chen X, Chi YR. NHC-catalyzed reactions of enals with water as a solvent Green Chemistry. 15: 1505. DOI: 10.1039/C3GC40397A |
0.351 |
|
2013 |
Chen X, Fang X, Chi YR. ChemInform Abstract: cis-Enals in N-Heterocyclic Carbene-Catalyzed Reactions: Distinct Stereoselectivity and Reactivity. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201345044 |
0.735 |
|
2013 |
Leong WWY, Chen X, Chi YR. ChemInform Abstract: NHC-Catalyzed Reactions of Enals with Water as a Solvent. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201340091 |
0.367 |
|
2012 |
Mo J, Chen X, Chi YR. Oxidative γ-addition of enals to trifluoromethyl ketones: enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis. Journal of the American Chemical Society. 134: 8810-3. PMID 22571795 DOI: 10.1021/ja303618z |
0.635 |
|
2012 |
Hao L, Du Y, Lv H, Chen X, Jiang H, Shao Y, Chi YR. Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts. Organic Letters. 14: 2154-7. PMID 22486921 DOI: 10.1021/ol300676w |
0.717 |
|
2012 |
Tang Q, Chen X, Tiwari B, Chi YR. Addition of indoles to oxyallyl cations for facile access to α-indole carbonyl compounds. Organic Letters. 14: 1922-5. PMID 22455439 DOI: 10.1021/ol300591z |
0.746 |
|
2012 |
Zhang J, Tiwari B, Xing C, Chen X, Chi YR. Enantioselective oxidative cross-dehydrogenative coupling of tertiary amines to aldehydes. Angewandte Chemie (International Ed. in English). 51: 3649-52. PMID 22389195 DOI: 10.1002/Anie.201109054 |
0.77 |
|
2011 |
Fang X, Chen X, Lv H, Chi YR. Enantioselective Stetter reactions of enals and modified chalcones catalyzed by N-heterocyclic carbenes. Angewandte Chemie (International Ed. in English). 50: 11782-5. PMID 21990276 DOI: 10.1002/Anie.201105812 |
0.767 |
|
2011 |
Fang X, Chen X, Chi YR. Enantioselective Diels-Alder reactions of enals and alkylidene diketones catalyzed by N-heterocyclic carbenes. Organic Letters. 13: 4708-11. PMID 21809839 DOI: 10.1021/Ol201917U |
0.783 |
|
2011 |
Liu W, Zhou J, Zheng C, Chen X, Xiao H, Yang Y, Guo Y, Zhao G. Tandem cross-Rauhut–Currier/cyclization reactions of activated alkenes to give densely functionalized 3,4-dihydropyrans Tetrahedron. 67: 1768-1773. DOI: 10.1016/J.Tet.2011.01.036 |
0.531 |
|
2011 |
Liu W, Zhou J, Zheng C, Chen X, Xiao H, Yang Y, Guo Y, Zhao G. ChemInform Abstract: Tandem Cross-Rauhut-Currier/Cyclization Reactions of Activated Alkenes to Give Densely Functionalized 3,4-Dihydropyrans. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201126144 |
0.405 |
|
2010 |
Yang YQ, Chai Z, Wang HF, Chen XK, Cui HF, Zheng CW, Xiao H, Li P, Zhao G. Chiral primary-secondary diamines catalyzed Michael-aldol-dehydration reaction between benzoylacetates and alpha,beta-unsaturated ketones: highly enantioselective synthesis of functionalized chiral cyclohexenones. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 13295-8. PMID 19908264 DOI: 10.1002/Chem.200901541 |
0.386 |
|
2010 |
Chen X, Zheng C, Zhao S, Chai Z, Yang Y, Zhao G, Cao W. ChemInform Abstract: Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to β,γ-Unsaturated α-Keto Esters. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201050022 |
0.346 |
|
2010 |
Zheng C, Lu Y, Zhang J, Chen X, Chai Z, Ma W, Zhao G. ChemInform Abstract: The Enantioselective Organocatalyzed Diels-Alder Reaction of 2-Vinylindoles with α,β-Unsaturated Aldehydes: An Efficient Route to Functionalized Tetrahydrocarbazoles. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201039122 |
0.47 |
|
2010 |
Yang Y, Chai Z, Wang H, Chen X, Cui H, Zheng C, Xiao H, Li P, Zhao G. ChemInform Abstract: Chiral Primary-Secondary Diamines Catalyzed Michael-Aldol-Dehydration Reaction Between Benzoylacetates and α,β-Unsaturated Ketones: Highly Enantioselective Synthesis of Functionalized Chiral Cyclohexenones. Cheminform. 41. DOI: 10.1002/chin.201018062 |
0.502 |
|
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