Compounds > pyrroles
Page last updated: 2024-08-18

pyrroles and longamide b

pyrroles has been researched along with longamide b in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Minassian, F; Patel, J; Pelloux-Léon, N; Vallée, Y1
Dong, G; Trost, BM1
Dong, G; Osipov, M; Trost, BM1
Ding, L; Du, Z; Ma, YY; Peng, W; Zhang, K; Zhang, Y; Zhao, DG; Zhou, AY1
Fujimoto, Y; Fukase, K; Inuki, S; Kashiwabara, E; Shiokawa, Z; Yoshidome, D1

Other Studies

5 other study(ies) available for pyrroles and longamide b

ArticleYear
Syntheses of S-enantiomers of hanishin, longamide B, and longamide B methyl ester from L-aspartic acid beta-methyl ester: establishment of absolute stereochemistry.
    The Journal of organic chemistry, 2005, Oct-28, Volume: 70, Issue:22

    Topics: Aspartic Acid; Esters; Molecular Structure; Pyrroles; Stereoisomerism

2005
Asymmetric annulation toward pyrrolopiperazinones: concise enantioselective syntheses of pyrrole alkaloid natural products.
    Organic letters, 2007, Jun-07, Volume: 9, Issue:12

    Topics: Molecular Structure; Piperazines; Pyrroles; Stereoisomerism

2007
Palladium-catalyzed dynamic kinetic asymmetric transformations of vinyl aziridines with nitrogen heterocycles: rapid access to biologically active pyrroles and indoles.
    Journal of the American Chemical Society, 2010, Nov-10, Volume: 132, Issue:44

    Topics: Aziridines; Catalysis; Drug Design; Heterocyclic Compounds; Indoles; Molecular Structure; Nitrogen; Palladium; Pyrroles; Vinyl Compounds

2010
Total synthesis and cytotoxic activities of longamide B, longamide B methyl ester, hanishin, and their analogues.
    Bioorganic & medicinal chemistry letters, 2016, Jan-01, Volume: 26, Issue:1

    Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Humans; Molecular Structure; Pyrroles; Structure-Activity Relationship

2016
Discovery of a Novel Scaffold as an Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitor Based on the Pyrrolopiperazinone Alkaloid, Longamide B.
    ChemMedChem, 2016, 12-16, Volume: 11, Issue:24

    Topics: Drug Discovery; Enzyme Activation; Enzyme Inhibitors; Indoleamine-Pyrrole 2,3,-Dioxygenase; Matrix Attachment Regions; Models, Molecular; Piperazines; Pyrazoles; Pyrroles

2016