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For: Namjoshi OA, Cook JM. Sarpagine and Related Alkaloids. Alkaloids Chem Biol 2016;76:63-169. [PMID: 26827883 DOI: 10.1016/bs.alkal.2015.08.002] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 1.7] [Reference Citation Analysis]
Number Citing Articles
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2 Pandey KP, Rahman MT, Cook JM. Bisindole Alkaloids from the Alstonia Species: Recent Isolation, Bioactivity, Biosynthesis, and Synthesis. Molecules 2021;26:3459. [PMID: 34200196 DOI: 10.3390/molecules26113459] [Reference Citation Analysis]
3 Otogo N'Nang E, Le Pogam P, Ndong Mba T, Sima Obiang C, Mouray E, Grellier P, Kumulungui B, Champy P, Beniddir MA. Targeted Isolation of Hemitheion from Mostuea brunonis, a Proposed Biosynthetic Intermediate of Theionbrunonines. J Nat Prod 2021;84:1409-13. [PMID: 33825474 DOI: 10.1021/acs.jnatprod.1c00143] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Liu T, Feng J, Chen C, Deng Z, Kotagiri R, Zhou G, Zhang X, Cai Q. Copper(I)-Catalyzed Intramolecular Asymmetric Double C-Arylation for the Formation of Chiral Spirocyclic Bis-oxindoles. Org Lett 2019;21:4505-9. [DOI: 10.1021/acs.orglett.9b01373] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 3.7] [Reference Citation Analysis]
5 Mohammed AE, Abdul-Hameed ZH, Alotaibi MO, Bawakid NO, Sobahi TR, Abdel-Lateff A, Alarif WM. Chemical Diversity and Bioactivities of Monoterpene Indole Alkaloids (MIAs) from Six Apocynaceae Genera. Molecules 2021;26:488. [PMID: 33477682 DOI: 10.3390/molecules26020488] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
6 Rahman MT, Tiruveedhula VVNPB, Stephen MR, Rallapalli SK, Pandey KP, Cook JM. Completion of the Total Synthesis of Several Bioactive Sarpagine/Macroline Alkaloids including the Important NF-κB Inhibitor N4-Methyltalpinine. Molecules 2022;27:1738. [PMID: 35268836 DOI: 10.3390/molecules27051738] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Stephen MR, Rahman MT, Tiruveedhula VVNPB, Fonseca GO, Deschamps JR, Cook JM. Concise Total Synthesis of (-)-Affinisine Oxindole, (+)-Isoalstonisine, (+)-Alstofoline, (-)-Macrogentine, (+)-Na -Demethylalstonisine, (-)-Alstonoxine A, and (+)-Alstonisine. Chemistry 2017;23:15805-19. [PMID: 28875520 DOI: 10.1002/chem.201703572] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 2.4] [Reference Citation Analysis]
8 Rahman MT, Deschamps JR, Imler GH, Schwabacher AW, Cook JM. Total Synthesis of Macrocarpines D and E via an Enolate-Driven Copper-Mediated Cross-Coupling Process: Replacement of Catalytic Palladium with Copper Iodide. Org Lett 2016;18:4174-7. [PMID: 27526647 DOI: 10.1021/acs.orglett.6b01526] [Cited by in Crossref: 17] [Cited by in F6Publishing: 8] [Article Influence: 2.8] [Reference Citation Analysis]
9 Dagoneau D, Wang Q, Zhu J. Towards the Sarpagine-Ajmaline-Macroline Family of Indole Alkaloids: Enantioselective Synthesis of an N-Demethyl Alstolactone Diastereomer. Chemistry 2020;26:4866-73. [PMID: 32065430 DOI: 10.1002/chem.202000415] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Chen W, Ma Y, He W, Wu Y, Huang Y, Zhang Y, Tian H, Wei K, Yang X, Zhang H. Structure units oriented approach towards collective synthesis of sarpagine-ajmaline-koumine type alkaloids. Nat Commun 2022;13:908. [PMID: 35177620 DOI: 10.1038/s41467-022-28535-x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Dang TT, Franke J, Carqueijeiro IST, Langley C, Courdavault V, O'Connor SE. Sarpagan bridge enzyme has substrate-controlled cyclization and aromatization modes. Nat Chem Biol 2018;14:760-3. [PMID: 29942076 DOI: 10.1038/s41589-018-0078-4] [Cited by in Crossref: 19] [Cited by in F6Publishing: 13] [Article Influence: 4.8] [Reference Citation Analysis]
12 Lim H, Seong S, Kim Y, Seo S, Han S. Biopatterned Reorganization of Alkaloids Enabled by Ring-Opening Functionalization of Tertiary Amines. J Am Chem Soc 2021;143:19966-74. [PMID: 34784466 DOI: 10.1021/jacs.1c10205] [Reference Citation Analysis]
13 Meloche JL, Ashfeld BL. A Rhodium(II)-Catalyzed Formal [4+1]-Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4-Dipoles. Angew Chem Int Ed Engl 2017;56:6604-8. [PMID: 28466963 DOI: 10.1002/anie.201701147] [Cited by in Crossref: 30] [Cited by in F6Publishing: 17] [Article Influence: 6.0] [Reference Citation Analysis]
14 Rahman MT, Tiruveedhula VV, Cook JM. Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review. Molecules 2016;21:E1525. [PMID: 27854259 DOI: 10.3390/molecules21111525] [Cited by in Crossref: 26] [Cited by in F6Publishing: 17] [Article Influence: 4.3] [Reference Citation Analysis]
15 Meloche JL, Ashfeld BL. A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles. Angew Chem 2017;129:6704-8. [DOI: 10.1002/ange.201701147] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
16 Nguyen TD, Dang TT. Cytochrome P450 Enzymes as Key Drivers of Alkaloid Chemical Diversification in Plants. Front Plant Sci 2021;12:682181. [PMID: 34367208 DOI: 10.3389/fpls.2021.682181] [Reference Citation Analysis]