Four new norlignan glycoside isomers from the twigs of Cephalotaxus oliveri Mast
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Qing-Wen Zhang | Hui Liu | Xiao‐Jun Huang | Fancheng Meng | D. Ren | Ligen Lin | Qingqing Zeng | Chang Yu
[1] Qing-Wen Zhang,et al. Chemistry, Bioactivity, and the Structure-Activity Relationship of Cephalotaxine-Type Alkaloids From Cephalotaxus sp. , 2017 .
[2] Xing Zhang,et al. Antiphytoviral activity of alkaloids from Cephalotaxus sinensis , 2016 .
[3] Qing-Wen Zhang,et al. New cycloartane triterpene glycosides from Thalictrum ramosum , 2016 .
[4] V. Rana,et al. Essential oil of Cephalotaxus griffithii needle inhibits proliferation and migration of human cervical cancer cells: involvement of mitochondria-initiated and death receptor-mediated apoptosis pathways , 2015, Natural product research.
[5] Weidong Zhang,et al. Diterpenoid lanceolatins A–G from Cephalotaxus lanceolata and their anti-inflammatory and anti-tumor activities , 2015 .
[6] C. Chung. Omacetaxine for treatment-resistant or treatment-intolerant adult chronic myeloid leukemia. , 2014, American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists.
[7] A. Hoveyda,et al. A Broadly Applicable NHC–Cu-Catalyzed Approach for Efficient, Site-, and Enantioselective Coupling of Readily Accessible (Pinacolato)alkenylboron Compounds to Allylic Phosphates and Applications to Natural Product Synthesis , 2014, Journal of the American Chemical Society.
[8] E. Carreira,et al. Iridium-catalyzed enantioselective allylic vinylation. , 2013, Journal of the American Chemical Society.
[9] Hajer Abdelkafi,et al. Natural products from Cephalotaxus sp.: chemical diversity and synthetic aspects. , 2012, Natural product reports.
[10] L. Vrijmoed,et al. Antioxidant activities and phenolic constituents of Cephalotaxus oliveri Mast. aerial parts , 2012 .
[11] A. Hoveyda,et al. Stereoisomerically pure trisubstituted vinylaluminum reagents and their utility in copper-catalyzed enantioselective synthesis of 1,4-dienes containing Z or E alkenes. , 2010, Angewandte Chemie.
[12] S. Christensen,et al. Structure and absolute configuration of nyasol and hinokiresinol via synthesis and vibrational circular dichroism spectroscopy. , 2005, Journal of natural products.
[13] A. Nikolaev,et al. Synthesis of carbohydrate mimetics of an acceptor substrate for the Leishmania elongating α-d-mannopyranosylphosphate transferase , 2000 .
[14] T. Akiyama,et al. Stereochemistry of cis- and trans-hinokiresinol and their estrogen-like activity. , 2000, Chemical & pharmaceutical bulletin.
[15] G. Tanabe,et al. Enantioselective total synthesis of the di-O-methyl ethers of (–)-agatharesinol, (+)-hinokiresinol and (–)-sugiresinol, characteristic norlignans of Coniferae , 1996 .
[16] I. Messana,et al. Mononyasine A and mononyasine B: Two glucosides from Hypoxis nyasica , 1989 .
[17] C. Enzell,et al. The chemistry of the order araucariales 7. Mass spectrometric fragmentation of diphenylpentaneresinols , 1967 .
[18] N. Oishi,et al. The structure of hinokiresinol , 1965 .