Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Cajanusine"'
Publikováno v:
J Am Chem Soc
The first enantioselective synthesis of (−)-cajanusine is presented. Key features of the route include a rapid synthesis of the [4.2.0] bicyclooctane core by an enantioselective isomerization/stereoselective [2+2]-cycloaddition strategy as well as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbc85847cca70225149ab2044fc0f438
https://doi.org/10.1021/jacs.0c00359
https://doi.org/10.1021/jacs.0c00359
Autor:
Yao-Lan Li, et al. et al.
Publikováno v:
ChemInform. 45
Both enantiomers exhibit inhibitory activities on the growth of hepatocellular carcinoma cells.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3833f98fc66c27325a1015d4caea5532
https://doi.org/10.1002/chin.201423216
https://doi.org/10.1002/chin.201423216
Autor:
Yu-Qing Jian, Ying-Jie Li, Xiao-Long Li, Xiao-Jun Huang, Ying Wang, Bing-Xin Zhao, Yao-Lan Li, Dong-Mei Zhang, Wen-Cai Ye, Ren-Wang Jiang
Publikováno v:
Organic letters. 16(1)
A pair of new enantiomeric stilbene dimers, (+)- and (-)-cajanusine [(+)-1 and (-)-1], with a unique coupling pattern were isolated from the leaves of Cajanus cajan . Their structures including absolute configurations were elucidated on the basis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37b59fae6013309984f8e71b53f5d66e
https://pubmed.ncbi.nlm.nih.gov/24295169
https://pubmed.ncbi.nlm.nih.gov/24295169