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For: Dong S, Liu X, Feng X. Asymmetric Catalytic Rearrangements with α-Diazocarbonyl Compounds. Acc Chem Res 2022;55:415-28. [PMID: 35029358 DOI: 10.1021/acs.accounts.1c00664] [Cited by in Crossref: 32] [Cited by in F6Publishing: 34] [Article Influence: 32.0] [Reference Citation Analysis]
Number Citing Articles
1 Liu X, Liu LG, Chen CM, Li X, Xu Z, Lu X, Zhou B, Ye LW. Copper-Catalyzed Enantioselective Doyle-Kirmse Reaction of Azide-Ynamides via α-Imino Copper Carbenes. Angew Chem Int Ed Engl 2023;:e202216923. [PMID: 36639865 DOI: 10.1002/anie.202216923] [Reference Citation Analysis]
2 Liang YX, Wang J, Xu XC, Gong Y, Zhao YL. Lewis Acid Mediated Conjugate Addition of Isocyanides to β-Hydroxy-α-diazo Carbonyls: Synthesis of β-Carboxamido-α-diazo Carbonyl Compounds. Org Lett 2023;25:200-4. [PMID: 36546845 DOI: 10.1021/acs.orglett.2c04050] [Reference Citation Analysis]
3 Zhong Z, Ning L, Lu Y, Tan J, Lin L, Feng X. Asymmetric catalytic alkylation of vinyl azides with 3-bromo oxindoles: water-assisted chemo- and enantiocontrol. Sci China Chem 2023. [DOI: 10.1007/s11426-022-1500-0] [Reference Citation Analysis]
4 Mo Y, Chen Q, Li J, Ye D, Zhou Y, Dong S, Liu X, Feng X. Asymmetric Catalytic Conjugate Addition of Cyanide to Chromones and β-Substituted Cyclohexenones. ACS Catal 2022. [DOI: 10.1021/acscatal.2c05509] [Reference Citation Analysis]
5 Ali A, Harit HK, Devi M, Ghosh D, Singh RP. Ring Expansion of Isatins via 1,2-Phospha-Brook Rearrangement: A Route to the Synthesis of 2-Quinolinone-Derived p-Quinone Methides. J Org Chem 2022;87:16313-27. [PMID: 36459618 DOI: 10.1021/acs.joc.2c01929] [Reference Citation Analysis]
6 Hou L, Zhou Y, Yu H, Zhan T, Cao W, Feng X. Enantioselective Radical Addition to Ketones through Lewis Acid-Enabled Photoredox Catalysis. J Am Chem Soc 2022;144:22140-9. [PMID: 36414018 DOI: 10.1021/jacs.2c09691] [Reference Citation Analysis]
7 Xie J, Suleman M, Zhang K, Lu P, Wang Y. Synthesis of Functionalized Indolobenzazepinones via Sc(OTf)3-Induced Ring Expansion/Annulation Reactions of 4-Diazoisoquinolin-3-ones with Isatins. J Org Chem 2022. [DOI: 10.1021/acs.joc.2c02076] [Reference Citation Analysis]
8 Kubiak RW 2nd, Tracy WF, Alford JS, Davies HML. Asymmetric Cyclopropanation with 4-Aryloxy-1-sulfonyl-1,2,3-triazoles: Expanding the Range of Rhodium-Stabilized Donor/Acceptor Carbenes to Systems with an Oxygen Donor Group. J Org Chem 2022;87:13517-28. [PMID: 36264239 DOI: 10.1021/acs.joc.2c00978] [Reference Citation Analysis]
9 Qi M, Suleman M, Fan J, Lu P, Wang Y. Cu(I)-catalyzed synthesis of spiro[isoquinoline-4,2'-[1,3]oxazin]-3-ones via ring expansion reactions of isoxazoles with 4-diazoisoquinolin-3-ones. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.133092] [Reference Citation Analysis]
10 Yun R, Li T, He L, Shi C, Xu R. Atomically Dispersed Iron Sites on the Hollow Nitrogen-Doped Carbon Framework with a Highly Efficient Performance on Carbon Dioxide Cycloaddition. Inorg Chem 2022. [PMID: 36178332 DOI: 10.1021/acs.inorgchem.2c02695] [Reference Citation Analysis]
11 Wang W, Zhang F, Liu Y, Feng X. Diastereo‐ and Enantioselective Construction of Vicinal All‐Carbon Quaternary Stereocenters via Iridium/Europium Bimetallic Catalysis. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202208837] [Reference Citation Analysis]
12 Cai BG, Yao WZ, Li L, Xuan J. Visible-Light-Induced Imide Synthesis through a Nitrile Ylide Formation/Trapping Cascade. Org Lett 2022. [PMID: 36053175 DOI: 10.1021/acs.orglett.2c02671] [Reference Citation Analysis]
13 Wang T, Chen X, Zhu D, Chung LW, Xu M. Rhodium(I) Carbene‐Promoted Enantioselective C−H Functionalization of Simple Unprotected Indoles, Pyrroles and Heteroanalogues: New Mechanistic Insights. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202207008] [Reference Citation Analysis]
14 Yang W, Yang Z, Chen L, Lu Y, Zhang C, Su Z, Liu X, Feng X. Chiral nickel(II) complex catalyzed asymmetric [3 + 2] cycloaddition of α-diazo pyrazoleamides with 2-siloxy-1-alkenes. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.107791] [Reference Citation Analysis]
15 Xie D, Chen H, Wei D, Wei B, Li Z, Zhang J, Yu W, Han B. Regioselective Fluoroalkylphosphorylation of Unactivated Alkenes by Radical‐Mediated Alkoxyphosphine Rearrangement**. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202203398] [Reference Citation Analysis]
16 Lin Q, Zheng S, Chen L, Wu J, Li J, Liu P, Dong S, Liu X, Peng Q, Feng X. Catalytic Regio‐ and Enantioselective Protonation for the Synthesis of Chiral Allenes: Synergistic Effect of the Counterion and Water. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202203650] [Reference Citation Analysis]
17 Devi L, Kumar P, Kant R, Rastogi N. Exploiting the umpolung reactivity of diazo groups: direct access to triazolyl-azaarenes from azaarenes. Chem Commun (Camb) 2022;58:7062-5. [PMID: 35648386 DOI: 10.1039/d2cc01897g] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Liu Z, Sivaguru P, Zanoni G, Bi X. N-Triftosylhydrazones: A New Chapter for Diazo-Based Carbene Chemistry. Acc Chem Res 2022. [PMID: 35675648 DOI: 10.1021/acs.accounts.2c00186] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
19 Chen CY, Zhao JH, Xiong LX, Wang F, Yang G, Ma C. Borane-catalyzed arylation of aryldiazoacetates with N,N-dialkylanilines. Org Biomol Chem 2022;20:4101-4. [PMID: 35537202 DOI: 10.1039/d2ob00447j] [Reference Citation Analysis]
20 Lin Q, Zheng S, Chen L, Wu J, Li J, Liu P, Dong S, Liu X, Peng Q, Feng X. Catalytic Regio‐ and Enantioselective Protonation for the Synthesis of Chiral Allenes: Synergistic Effect of the Counterion and Water. Angewandte Chemie. [DOI: 10.1002/ange.202203650] [Reference Citation Analysis]
21 Tan Z, Zhu S, Liu Y, Feng X. Photoinduced Chemo‐, Site‐ and Stereoselective α‐C(sp 3 )−H Functionalization of Sulfides. Angewandte Chemie. [DOI: 10.1002/ange.202203374] [Reference Citation Analysis]
22 Lin X, Pu M, Sang X, Li S, Liu X, Wu YD, Feng X. Asymmetric Catalytic (2+1) Cycloaddition of Thioketones to Synthesize Tetrasubstituted Thiiranes. Angew Chem Int Ed Engl 2022;61:e202201151. [PMID: 35218131 DOI: 10.1002/anie.202201151] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
23 He C, Tang X, He X, Zhou Y, Liu X, Feng X. Regio- and enantioselective conjugate addition of β-nitro α,β-unsaturated carbonyls to construct 3-alkenyl disubstituted oxindoles. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.05.001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Ke C, Cao Q, Luo Y, Liu X, Feng X. Catalytic asymmetric amination of azlactones with azobenzenes. Chem Commun (Camb) 2022. [PMID: 35470829 DOI: 10.1039/d2cc01656g] [Reference Citation Analysis]
25 Tan Z, Zhu S, Liu Y, Feng X. Photoinduced Chemo-, Site- and Stereoselective α-C(sp3 )-H Functionalization of Sulfides. Angew Chem Int Ed Engl 2022;:e202203374. [PMID: 35445505 DOI: 10.1002/anie.202203374] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
26 Yu H, Zhan T, Zhou Y, Chen L, Liu X, Feng X. Visible-Light-Activated Asymmetric Addition of Hydrocarbons to Pyridine-Based Ketones. ACS Catal 2022;12:5136-44. [DOI: 10.1021/acscatal.2c00789] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
27 Zhang F, Ren B, Liu Y, Feng X. A nickel( ii )-catalyzed enantioselective all-carbon-based inverse-electron-demand Diels–Alder reaction of 2-pyrones with indenes. Org Chem Front . [DOI: 10.1039/d2qo00493c] [Reference Citation Analysis]
28 Dong P, Li Z, Liu X, Dong S, Feng X. Asymmetric synthesis of polycyclic spiroindolines via the Dy-catalyzed cascade reaction of 3-(2-isocyanoethyl)indoles with aziridines. Org Chem Front . [DOI: 10.1039/d2qo00874b] [Reference Citation Analysis]
29 Teng M, Han T, Huang E, Ye L. Research Progress on Enantioselective Desymmetrization Reactions Involving Metal Carbenes. Chinese Journal of Organic Chemistry 2022;42:3295. [DOI: 10.6023/cjoc202206041] [Reference Citation Analysis]