Areas of Focus
- Natural Product Chemistry
- Natural Organic Chemistry
Work Experience
- 1999-05 to Present - Shanghai Institute of Materia Medica, Chinese Academy of Sciences - Researcher
- 1996-05 to 1999-04 - Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences and Unilever Joint Laboratory - Senior Researcher and Project Leader
- 1994-10 to 1996-04 - Kunming Institute of Botany, Chinese Academy of Sciences - Associate Researcher
- 1993-08 to 1994-10 - University of Bristol, School of Chemistry - Postdoctoral Researcher
- 1991-03 to 1993-08 - Kunming Institute of Botany, Chinese Academy of Sciences - Postdoctoral Researcher
Academic Background & Achievements
- 1984-08 to 1990-07 PhD in Science: Lanzhou University
- 1980-09 to 1984-07 Bachelor's in Science: Lanzhou University
Publications
- Cascarinoids A-C, a Class of Diterpenoid Alkaloids with Unpredicted Conformations from Croton cascarilloides, Jianmin Yue, 2018
- Structural Elucidation and Bioinspired Total Syntheses of Ascorbylated Diterpenoid Hongkonoids A-D, Jianmin Yue, 2018
- Fortunoids A-C, Three Sesquiterpenoid Dimers with Different Carbon Skeletons from Chloranthus fortune, Jianmin Yue, 2017
- Phainanolide A, Highly Modified and Oxygenated Triterpenoid with Unique Motifs from Phyllanthus hainanensis, Jianmin Yue, 2017
- Mannolides A-C with an Intact Diterpenoid Skeleton Providing Insights on the Biosynthesis of Antitumor Cephalotaxus Troponoids, Jianmin Yue, 2016
- Cipacinoids A-D, Four Limonoids with Spirocyclic Skeletons from Cipadessa cinerascens, Jianmin Yue, 2016
- Himalensines A and B, Alkaloids with Unprecedented Carbon Skeletons from Daphniphyllum himalense, Jianmin Yue, 2016
- Ciliatonoids A and B, Two Limonoids from Toona ciliate, Jianmin Yue, 2016
- Phainanoids A-F, A New Class of Potent Immunosuppressive Triterpenoids with an Unprecedented Carbon Skeleton from Phyllanthus hainanensis, Jianmin Yue, 2015
- Flueggether A and Virosinine A, Anti-HIV Alkaloids from Flueggea virosa, Jianmin Yue, 2015
- Organic Carbonates from Natural Sources, Jianmin Yue, 2014
- Aphadilactones A-D, Four Diterpenoid Dimers with DGAT Inhibitory and Antimalarial Activities from a Meliaceae Plant, Jianmin Yue, 2014
- Logeracemin A, an Anti-HIV Daphniphyllum Alkaloid Dimer with a New Carbon Skeleton from Daphniphyllum longeracemosum, Jianmin Yue, 2014
- Ivorenolide B, an Immunosuppressive 17-Membered Macrolide from Khaya ivorensis: Structural Determination and Total Synthesis, Jianmin Yue, 2014
- Trichiconins A-C, Limonoids with New Carbon Skeletons from Trichilia connaroides, Jianmin Yue, 2014
- Laevinoids A and B: Two Diterpenoids with an Unprecedented Backbone from Croton laevigatus, Jianmin Yue, 2013
- Fluevirosines A-C: a biogenesis inspired example in the discovery of new bioactive scaffolds from Flueggea virosa., Jianmin Yue, 2013
- Walsucochinoids A and B: Novel Rearranged Limonoids from Walsura cochinchinensis, Jianmin Yue, 2012
- Ivorenolide A, an Unprecedented Immunosuppressive Macrolide from Khaya ivorensis: Structural Elucidation and Bioinspired Total Synthesis, Jianmin Yue, 2012
- Potent HGF/c-Met Axis Inhibitors from Eucalyptus globules: the Coupling of Phloroglucinol and Sesquiterpenoid Is Essential for the Activity, Jianmin Yue, 2012
- Chukrasones A and B: Potential Kv1.2 Potassium Channel Blockers with New Skeletons from Chukrasia tabularis, Jianmin Yue, 2012
- Serratustones A and B Representing a New Dimerization Pattern of Two Types of Sesquiterpenoids from Chloranthus serratus, Jianmin Yue, 2012
- Meliarachins A-K: Eleven Limonoids from the Twigs and Leaves of Melia azedarach, Jianmin Yue, 2011
- Phragmalin-Type Limonoid Orthoesters from the Twigs of Swietenia macrophylla, Jianmin Yue, 2011
- Ring A-seco triterpenoids with antibacterial activity from Dysoxylum hainanense, Jianmin Yue, 2011
- Sarcanolides A and B: two sesquiterpenoid dimers with a nonacyclic scaffold from Sarcandra hainanensis, Jianmin Yue, 2011
- Daphnane-Type Diterpenoids from Trigonostemon howii, Jianmin Yue, 2011
- Aphanamolide A, a New Limonoid from Aphanamixis polystachya, Jianmin Yue, 2011
- Onoceranoid-Type Triterpenoids from Lansium domesticum, Jianmin Yue, 2011
- Limonoids and Diterpenoids from Toona ciliata Roem. var. yunnanensis, Jianmin Yue, 2011
- Trigoxyphins A-G: Seven Diterpenes from Trigonostemon xyphophylloides, Jianmin Yue, 2010
- Mesendanins A-J:Ten Limonoids from the Twigs and Leaves of Melia toosendan, Jianmin Yue, 2010
- Sesquiterpenes and Dimeric Sesquiterpenoids from Sarcandra glabra, Jianmin Yue, 2010
- Limonoids and Triterpenoids from Khaya senegalensis, Jianmin Yue, 2010
- Mulavanins A-E: Limonoids from Munronia delavayi, Jianmin Yue, 2010
- Structure Determination of Grandifotane A from Khaya grandifoliola by NMR, X-ray Diffraction, and ECD Calculation, Jianmin Yue, 2010
- Multistalides A and B, two novel sesquiterpenoid dimers from Chloranthus multistachys, Jianmin Yue, 2010
- Trigochinins A-C: Three Novel Daphnane-type Diterpenes from Trigonostemon chinensis, Jianmin Yue, 2010
- Trigochinins D-I: six new daphnane-type diterpenoids from Trigonostemon chinensis, Jianmin Yue, 2010
- Three New Terpenoids from Pinus yunnanensis, Jianmin Yue, 2010
- Two Limonoids, Khayalenoids, A and B with an Unprecedented 8-Oxa-tricyclo4.3.2.0(2,7)undecane Motif, from Khaya senegalensis, Jianmin Yue, 2009
- Structurally Diverse Limonoids from the Fruits of Swietenia mahagoni, Jianmin Yue, 2009
- Harrisotones A-E, five novel prenylated polyketides with a rare spirocyclic skeleton from Harrisonia perforata, Jianmin Yue, 2009
- Limonoids from Khaya ivorensis, Jianmin Yue, 2009
- Cinnacassides A-E, five geranylphenylacetate glycosides from Cinnamomum cassia, Jianmin Yue, 2009
- Calycinumines A and B, Two Novel Alkaloids from Daphniphyllum calycinum, Jianmin Yue, 2009
- Plant Orthoesters, Jianmin Yue, 2009
- D-Ring-Opened Phragmalin-Type Limonoid Orthoesters from the Twigs of Swietenia macrophylla, Jianmin Yue, 2009
- Ring-A Modified Triterpenoids from Dysoxylum hainanense, Jianmin Yue, 2009
- Trigochilides A and B, Two Highly Modified Daphnane-Type Diterpenoids from Trigonostemon
Awards
- National Natural Science Award, Second Prize (2013)
- Shanghai Natural Science Award, First Prize (2010)
