نتائج البحث - "Xiao, Bing"

1

دورية أكاديمية

Stereoregular poly(2-phenylthiirane) via cationic ring-opening polymerization.

المؤلفون: Yu Xiao, Tian-Jun Yue, Xiao-Bing Lu, Wei-Min Ren

المصدر: Chemical Communications; 5/11/2024, Vol. 60 Issue 38, p5034-5037, 4p

مصطلحات موضوعية: ADDITION polymerization, RING-opening polymerization, STEREOCHEMISTRY

2

Beetleane A and Epicoane A: Two Carbon Skeletons Produced by Epicoccum nigrum

المؤلفون: Ling-Yi Kong, Yong-Qin Zhao, Yi-Lei Zheng, Ming-Hua Yang, Meihui Zhang, Ting Yang, Hao Zhang, Peng-Ran Cao, Xiao-Bing Wang, Yu-Cheng Gu

المصدر: Organic Letters. 23:3274-3277

مصطلحات موضوعية: biology, 010405 organic chemistry, Stereochemistry, Organic Chemistry, chemistry.chemical_element, 010402 general chemistry, Ring (chemistry), biology.organism_classification, 01 natural sciences, Biochemistry, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Physical and Theoretical Chemistry, Cycloheptane, Epicoccum nigrum, Carbon

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b6bf37217e5f154c6f81501da0f51d17Test
https://doi.org/10.1021/acs.orglett.1c00731Test

3

Pd-Catalyzed Enantioselective Tandem C–C Bond Activation/Cacchi Reaction between Cyclobutanones and o-Ethynylanilines

المؤلفون: Zhan-Jiang Zheng, Wan-Er Gan, Kun-Long Song, Li-Wen Xu, Xiao-Bing Chen, Wan-Chun Yang, Jian Cao, Bin Wu

المصدر: Organic Letters. 23:1309-1314

مصطلحات موضوعية: Indole test, Tandem, 010405 organic chemistry, Chemistry, Stereochemistry, Organic Chemistry, Enantioselective synthesis, 010402 general chemistry, 01 natural sciences, Biochemistry, 0104 chemical sciences, Catalysis, Stereocenter, Moiety, Physical and Theoretical Chemistry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0a7dca02f6fbb7c1255c033c6816e797Test
https://doi.org/10.1021/acs.orglett.0c04297Test

4

Hyperberins A and B, Type B Polycyclic Polyprenylated Acylphloroglucinols with Bicyclo[5.3.1]hendecane Core from Hypericum beanii

المؤلفون: Wei-Jia Lu, Pengfei Tang, Wen-Jun Xu, Yanqiu Zhang, Jun Luo, Ling-Yi Kong, Xiao-Bing Wang, Hao Zhang

المصدر: Organic Letters. 21:8558-8562

مصطلحات موضوعية: Circular dichroism, Bicyclic molecule, 010405 organic chemistry, Stereochemistry, Organic Chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, 0104 chemical sciences, chemistry.chemical_compound, Biosynthesis, chemistry, Hypericum beanii, Physical and Theoretical Chemistry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0f8e6a033a54025053f19adef5b2ce23Test
https://doi.org/10.1021/acs.orglett.9b03098Test

5

Bioactive A-ring rearranged limonoids from the root barks of Walsura robusta

المؤلفون: Ming-Hua Yang, Jun Luo, Ling-Yi Kong, Fa-Liang An, Xiao-Bing Wang

المصدر: Acta Pharmaceutica Sinica B, Vol 9, Iss 3, Pp 545-556 (2019)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cccc224645fc09dd88505300022f4db3Test
http://www.sciencedirect.com/science/article/pii/S2211383518312243Test

6

Asperfuranones A-C, 3(2H)-furanone derivatives from the fungus Aspergillus sp. and the configuration reassignment of their eighteen analogues

المؤلفون: Ya-Rong Wu, Guo-Ping Yin, Ming-Hua Yang, Hong-Liang Gao, Ling-Yi Kong, Xiao-Bing Wang

المصدر: Fitoterapia. 134:196-200

مصطلحات موضوعية: Pharmacology, Aspergillus, Circular dichroism, Molecular Structure, biology, Strain (chemistry), Chemistry, Stereochemistry, Circular Dichroism, General Medicine, Fungus, biology.organism_classification, Mice, RAW 264.7 Cells, Drug Discovery, Animals, Benzofurans

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d84d71b32b01d9e2736e0f0cf3be4f74Test
https://doi.org/10.1016/j.fitote.2019.02.024Test

7

Artemisianins A-D, new stereoisomers of seco-guaianolide involved heterodimeric [4+2] adducts from Artemisia argyi induce apoptosis via enhancement of endoplasmic reticulum stress

المؤلفون: Chao Han, Jian-Guang Luo, Dong-Rong Zhu, Xiao-Bing Wang, Gui-Min Xue, Ling-Yi Kong

المصدر: Bioorganic Chemistry. 84:295-301

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2dda8d11229087c80688a375650951dTest
https://doi.org/10.1016/j.bioorg.2018.11.013Test

8

Ciliatasecones A–C, three rearranged limonoids from Toona ciliata var. yunnanensis

المؤلفون: Zhirong Cui, Shanshan Wei, Panpan Zhang, Xiao-Bing Wang, Li Heng, Ming-Hua Yang, Yi Li, Ling-Yi Kong, Jun Luo

المصدر: Organic & Biomolecular Chemistry. 17:555-560

مصطلحات موضوعية: chemistry.chemical_classification, biology, Stereochemistry, Organic Chemistry, Ether, Cleavage (embryo), Ring (chemistry), biology.organism_classification, Biochemistry, chemistry.chemical_compound, chemistry, visual_art, Furan, visual_art.visual_art_medium, Bark, Physical and Theoretical Chemistry, Oxygen bridge, Toona ciliata, Lactone

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60b370bc1c0247b55ea651707eda9107Test
https://doi.org/10.1039/c8ob02736fTest

9

Seven new cytotoxic phenylspirodrimane derivatives from the endophytic fungus Stachybotrys chartarum

المؤلفون: Hong Zhang, Ming-Hua Yang, Fang-fang Zhuo, Ling-Yi Kong, Xiao-Bing Wang, Yue-Hu Pei, Na Gao, Xiao-Bei Cheng

المصدر: RSC Advances. 9:3520-3531

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::adf0354a7d5961a75e9f52c1e7469e08Test
https://doi.org/10.1039/c8ra10195gTest

10

Two new prenylated C6–C3 compounds from Illicium micranthum Dunn

المؤلفون: Xiao-Bing Huang, Zhi-Hong Zhou, Xiao-Man Lv, Afsar Khan, Yi-Fen Wang, Tian Hua, Lu Liu

المصدر: Natural Product Research. 34:425-428

مصطلحات موضوعية: chemistry.chemical_classification, 010405 organic chemistry, Stereochemistry, Organic Chemistry, Illicium micranthum, Plant Science, Sesquiterpene lactone, 01 natural sciences, Biochemistry, 0104 chemical sciences, Analytical Chemistry, 010404 medicinal & biomolecular chemistry, chemistry, Prenylation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::de68b670ac8db735e6e8e50861819906Test
https://doi.org/10.1080/14786419.2018.1531860Test

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