Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Zhan‐Peng Ge"'
Autor:
Jun-Su Zhou, Long Cheng, Yuan Gao, Zhan-Peng Ge, Bin Zhou, Jing-Ya Li, Jin-Xin Zhao, Jian-Min Yue
Publikováno v:
Engineering, Vol 38, Iss , Pp 144-154 (2024)
Four new norditerpenoid heterodimers with different dimerization patterns—namely, trigofragiloids A–C (denoted as compounds 1–3) and (+)- and (−)-trigofragiloid D (compound 4)—and three new phenanthrenone norditerpenoids—namely, trigofrag
Externí odkaz:
https://doaj.org/article/84df797e52eb4b288900c5a9fe35258e
Publikováno v:
Chinese Journal of Chemistry. 40:1177-1184
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48940b11762b6a07774124ad0e0e56e1
https://doi.org/10.1002/cjoc.202100913
https://doi.org/10.1002/cjoc.202100913
Autor:
Zhan-Peng Ge, Bin Zhou, Flavia M. Zimbres, Reagan S. Haney, Qun-Fang Liu, Yan Wu, Maria B. Cassera, Jin-Xin Zhao, Jian-Min Yue
Publikováno v:
Organic & Biomolecular Chemistry. 20:9000-9009
Seventeen new cephalotane-type diterpenoids were isolated from Cephalotaxus fortunei var. alpina. Compounds 14 and 15 contain an unusual 7-oxabicyclo[4.1.1]octane moiety.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2095fe33cddf13bcbd7b288e8b714f18
https://doi.org/10.1039/d2ob01748b
https://doi.org/10.1039/d2ob01748b
Autor:
Zhan-Peng, Ge, Bin, Zhou, Flavia M, Zimbres, Reagan S, Haney, Qun-Fang, Liu, Yan, Wu, Maria B, Cassera, Jin-Xin, Zhao, Jian-Min, Yue
Publikováno v:
Organicbiomolecular chemistry. 20(45)
Seventeen new cephalotane-type diterpenoids, fortalides A-Q (1-17), along with five known analogues, were isolated from the seeds of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e992e4f4c460a3ffc22a7f4a278ee300
https://pubmed.ncbi.nlm.nih.gov/36330968
https://pubmed.ncbi.nlm.nih.gov/36330968
Publikováno v:
Angewandte Chemie International Edition. 60:9374-9378
Cephalodiones A-D (1-4), the first example of C19 -norditerpenoid dimers, were isolated and fully characterized from a Cephalotaxus plant. These new skeletal natural products shared a unique tricyclo[6.4.1.12,7 ]tetradeca-3,5,9,11-tetraene-13,14-dion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15a7286bcd2713a127919b14bd108ff2
https://doi.org/10.1002/anie.202015332
https://doi.org/10.1002/anie.202015332
Autor:
Jian-Min Yue, Yao-Yue Fan, Cheng-Hui Xu, Jian Ding, Guo-Cai Wang, Qun-Fang Liu, Zhan-Peng Ge, Hongchun Liu
Publikováno v:
Journal of Natural Products. 82:1565-1575
Seventeen new 17- nor-cephalotane-type diterpenoids, fortalpinoids A-Q (1-17), were isolated from the seeds of Cephalotaxus fortunei var. alpine. Compound 12 represents the first 17- nor-cephalotane-type diterpenoid featuring an 8-oxabicyclo[3.2.1]oc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a91bccfa15c4cd3844aa189f112828f5
https://doi.org/10.1021/acs.jnatprod.9b00059
https://doi.org/10.1021/acs.jnatprod.9b00059
Autor:
Zhan-Peng Ge, Yao-Yue Fan, Li-She Gan, Jing-Ya Li, Jian-Min Yue, Li Sheng, Kai-Long Ji, You-Kai Xu
Publikováno v:
The Journal of organic chemistry. 84(1)
Four highly rearranged labdane-type diterpenoids, maximumins A–D (1–4) possessing different new carbon skeletons, together with a biosynthetically related known analog 5 were isolated from Amomum maximum. The structures of new compounds with abso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e338b5d07dc1b245570cd70d6e22a287
https://pubmed.ncbi.nlm.nih.gov/30525625
https://pubmed.ncbi.nlm.nih.gov/30525625