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Cited by in F6Publishing
For: Li Z, Chen Y, Wang C, Xu G, Shao Y, Zhang X, Tang S, Sun J. Construction of C-C Axial Chirality via Asymmetric Carbene Insertion into Arene C-H Bonds. Angew Chem Int Ed Engl 2021;60:25714-8. [PMID: 34597448 DOI: 10.1002/anie.202110430] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Su J, Yan Z, Sun J. Rhodium-Catalyzed N-Arylation of 2-Pyridones Enabled by 1,6-Acyl Migratory Rearrangement of 2-Oxypyridines. Org Lett 2023;25:1974-7. [PMID: 36920185 DOI: 10.1021/acs.orglett.3c00519] [Reference Citation Analysis]
2 Chen Q, Huang T, Shao Y, Tang S, Sun J. Forming All-Carbon Quaternary Centers by Geminal Difunctionalization of Diazo Compounds with N,N-Disubstituted Anilines and Allylic Carbonates. J Org Chem 2023;88:3308-12. [PMID: 36760174 DOI: 10.1021/acs.joc.2c02730] [Reference Citation Analysis]
3 Choppin S, Wencel-Delord J. Sulfoxide-Directed or 3d-Metal Catalyzed C-H Activation and Hypervalent Iodines as Tools for Atroposelective Synthesis. Acc Chem Res 2023;56:189-202. [PMID: 36705934 DOI: 10.1021/acs.accounts.2c00573] [Reference Citation Analysis]
4 Ge Z, Lu B, Teng H, Wang X. Efficient Synthesis of Diaryl Quaternary Centers by Rh(II)/Xantphos Catalyzed Relay C-H Functionalization and Allylic Alkylation. Chemistry 2023;29:e202202820. [PMID: 36239082 DOI: 10.1002/chem.202202820] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Liu X, Tang Z, Si Z, Zhang Z, Zhao L, Liu L. Enantioselective para ‐C(sp 2 )−H Functionalization of Alkyl Benzene Derivatives via Cooperative Catalysis of Gold/Chiral Brønsted Acid**. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202208874] [Reference Citation Analysis]
6 Niu C, Zhou Y, Chen Q, Zhu Y, Tang S, Yu ZX, Sun J. Atroposelective Synthesis of N-Arylindoles via Enantioselective N-H Bond Insertion. Org Lett 2022. [PMID: 36190794 DOI: 10.1021/acs.orglett.2c03003] [Reference Citation Analysis]
7 Liu J, Li Q, Shao Y, Sun J. Atroposelective Synthesis of Axially Chiral C2-Arylindoles via Rhodium-Catalyzed Asymmetric C-H Bond Insertion. Org Lett 2022;24:4670-4. [PMID: 35730740 DOI: 10.1021/acs.orglett.2c01818] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Yang Y, Lu B, Xu G, Wang X. Overcoming O-H Insertion to Para-Selective C-H Functionalization of Free Phenols: Rh(II)/Xantphos Catalyzed Geminal Difunctionalization of Diazo Compounds. ACS Cent Sci 2022;8:581-9. [PMID: 35647279 DOI: 10.1021/acscentsci.2c00004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
9 Xu G, Huang M, Zhang T, Shao Y, Tang S, Cao H, Zhang X, Sun J. Asymmetric Arylation of Diazoesters with Anisoles Enabled by Cooperative Gold and Phosphoric Acid Catalysis. Org Lett 2022. [PMID: 35394288 DOI: 10.1021/acs.orglett.2c00709] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
10 Biswas A, Pan S, Samanta R. Cu(II)-Catalyzed Construction of Heterobiaryls using 1-Diazonaphthoquinones: A General Strategy for the Synthesis of QUINOX and Related P,N Ligands. Org Lett . [DOI: 10.1021/acs.orglett.2c00127] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
11 Rao J, Ren X, Zhu X, Guo Z, Wang C, Zhou C. Ruthenium-catalyzed reaction of diazoquinones with arylamines to synthesize diarylamines. Org Chem Front . [DOI: 10.1039/d2qo01134d] [Reference Citation Analysis]
12 Li F, Lu B, Liu Y, Wang X. Dirhodium/Xantphos-Catalyzed Tandem C—H Functionalization/Allylic Alkylation: Direct Access to 3-Acyl-3-allyl Oxindole Derivatives from N-Aryl-α-diazo-β-keto Amides. Chinese Journal of Organic Chemistry 2022;42:3390. [DOI: 10.6023/cjoc202206053] [Reference Citation Analysis]
13 Rao J, Zhao J, Zhu X, Guo Z, Wang C, Zhou C. Rhodium-catalyzed reaction of diazoquinones with allylboronates to synthesize allylphenols. Org Chem Front . [DOI: 10.1039/d2qo00626j] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]