BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Shaaban S, Merten C, Waldmann H. Catalytic Atroposelective C7 Functionalisation of Indolines and Indoles. Chemistry 2021. [PMID: 34676929 DOI: 10.1002/chem.202103365] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [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. [PMID: 36920185 DOI: 10.1021/acs.orglett.3c00519] [Reference Citation Analysis]
2 Fontaine JP, Lapointe V, Filliâtre M, Bélanger G. Synthesis of Substituted Indolines through Photocatalyzed Decarboxylative Radical Arylation. J Org Chem 2023. [PMID: 36877887 DOI: 10.1021/acs.joc.2c02627] [Reference Citation Analysis]
3 Flegel J, Shaaban S, Jia ZJ, Schulte B, Lian Y, Krzyzanowski A, Metz M, Schneidewind T, Wesseler F, Flegel A, Reich A, Brause A, Xue G, Zhang M, Dötsch L, Stender ID, Hoffmann JE, Scheel R, Janning P, Rastinejad F, Schade D, Strohmann C, Antonchick AP, Sievers S, Moura-Alves P, Ziegler S, Waldmann H. The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation. J Med Chem 2022;65:16268-89. [PMID: 36459434 DOI: 10.1021/acs.jmedchem.2c00956] [Reference Citation Analysis]
4 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]
5 Sarkar S, Samanta R. Weakly Coordinating tert-Amide-Assisted Ru(II)-Catalyzed Synthesis of Azacoumestans via Migratory Insertion of Quinoid Carbene: Application in the Total Synthesis of Isolamellarins. Org Lett 2022;24:4536-41. [PMID: 35735263 DOI: 10.1021/acs.orglett.2c01556] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
6 Yin S, Pan C, Zhang W, Liu C, Zhao F, Gu Q, You S. SCpRh(III)-Catalyzed Enantioselective Synthesis of Atropisomers by C2-Arylation of Indoles with 1-Diazonaphthoquinones. Org Lett . [DOI: 10.1021/acs.orglett.2c01141] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]