Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Xingchao Guan"'
Publikováno v:
The Journal of Organic Chemistry. 85:5724-5732
The nominal enantiomer of chlorabietol B was regio- and stereoselectively synthesized from (−)-abietic acid in 13 steps. Key features of the synthesis involved an oxidative [3+2] cycloaddition to i...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0d1ae7201416cc4c096046e98acd2eb
https://doi.org/10.1021/acs.joc.0c00233
https://doi.org/10.1021/acs.joc.0c00233
Publikováno v:
Synthesis. 51:1825-1831
This study extensively investigated the regioselective oxidative coupling reactions of 5-bromoisorhapontigenin catalyzed by FeCl3·6H2O or HRP/H2O2 in different solvent systems and the distinct reductive debromination of the isolated dimeric coupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffb99714adb5b9bcb27d362298e06be6
https://doi.org/10.1055/s-0037-1611713
https://doi.org/10.1055/s-0037-1611713
The asymmetric biomimetic synthesis of resveratrol dimers was preliminarily explored using the enzyme-mediated oxidative coupling reactions of chiral resveratrol derivatives as the key step. The horseradish peroxidase-H2O2-promoted oxidations of 11,1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0a11ca5fb3d0a92b6c96288c62bea9
Publikováno v:
The Journal of organic chemistry. 85(8)
The nominal enantiomer of chlorabietol B was regio- and stereoselectively synthesized from (-)-abietic acid in 13 steps. Key features of the synthesis involved an oxidative [3+2] cycloaddition to install the dihydrobenzofuran moiety and an Aldol reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e8366b6501153287233dcd1c60dd020
https://pubmed.ncbi.nlm.nih.gov/32212620
https://pubmed.ncbi.nlm.nih.gov/32212620
Publikováno v:
Tetrahedron. 74:4013-4019
FeCl3·6H2O-promoted biomimetic oxidations of 3,5-dihalogeno-resveratrol in different acetone systems produced several coupling intermediates bearing distinct dimeric skeletons with moderate yields. The subsequent deprotection reactions of brominated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::731b95d0fc2ea1adf07fef31e65b735c
https://doi.org/10.1016/j.tet.2018.06.005
https://doi.org/10.1016/j.tet.2018.06.005