Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Jing-Chun Han"'
Publikováno v:
Chemical Reviews. 123:4934-4971
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::139ee7e3a22317dbd822c56647fc0657
https://doi.org/10.1021/acs.chemrev.2c00763
https://doi.org/10.1021/acs.chemrev.2c00763
Publikováno v:
Tetrahedron. 75:1739-1745
The collective total synthesis of a series of botryanes, which are an important group of sesquiterpene antibiotics isolated from the metabolites of the fungus Botrytis cinerea, has been reported. The highly functionalized hydrindane skeleton of the b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2d3d63713431c1fe9a3e3ff04207127
https://doi.org/10.1016/j.tet.2018.11.019
https://doi.org/10.1016/j.tet.2018.11.019
Publikováno v:
Chemical reviews. 120(13)
Natural products containing eight-membered carbocycles constitute a class of structurally intriguing and biologically important molecules such as the famous diterpenes taxol and vinigrol. Such natural products are being increasingly investigated beca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad29041d1bc604e17c321a8af296d03
https://pubmed.ncbi.nlm.nih.gov/32343125
https://pubmed.ncbi.nlm.nih.gov/32343125
Publikováno v:
Tetrahedron. 73:3289-3303
The humulanolides are a series of sesquiterpene lactones, most of which have unique and challenging structure. The humulanolides have exhibited anticancer activity. The combinations of fascinating structural motifs and promising pharmacological prope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77fa40a0491a570ba100496916b44630
https://doi.org/10.1016/j.tet.2017.05.009
https://doi.org/10.1016/j.tet.2017.05.009
Publikováno v:
Tetrahedron. 73:3629-3635
A concise approach for the stereoselective construction of the oxa-pentacyclic core of solanoeclepin A has been developed by using the intramolecular Diels-Alder (IMDA) reaction from the furan-tethered dienophile.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b290078a597c4c11cfc9270447b524e2
https://doi.org/10.1016/j.tet.2017.03.090
https://doi.org/10.1016/j.tet.2017.03.090
Autor:
Jing-Chun Han, Chuang-Chuang Li
Publikováno v:
The Chemical Record. 17:499-517
In this account, we provide a brief summary of recent developments in ruthenium-catalyzed metathesis cascade reactions towards the total synthesis of natural products. We also highlight recent progress from our own laboratory regarding the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3f4df346c6455e2900e9f07e9fd229b
https://doi.org/10.1002/tcr.201600110
https://doi.org/10.1002/tcr.201600110
Publikováno v:
Organic Letters. 18:4932-4935
The first and catalytic enantioselective total synthesis of hypocrolide A (>99% ee) in 12 steps, as well as other botryanes, is described. The absolute configurations of these compounds have been unambiguously confirmed or reassigned accordingly. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c136cd40fe62b3ff1ce5fa9d27fe8af3
https://doi.org/10.1021/acs.orglett.6b02414
https://doi.org/10.1021/acs.orglett.6b02414
Autor:
Jing-Chun Han, Chuang-Chuang Li
Publikováno v:
Synlett. 26:1289-1304
This account describes our laboratory’s latest endeavors toward the collective synthesis of natural products. An overview of the general strategy is presented together with several total syntheses developed by our group. These examples demonstrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ae6cff1744dd8b1cb997997b85d3303
https://doi.org/10.1055/s-0034-1380180
https://doi.org/10.1055/s-0034-1380180
Publikováno v:
Journal of the American Chemical Society. 136:13610-13613
A new method has been developed for the concise and asymmetric synthesis of seven humulanolides in 5-7 steps without the need for protecting groups. Notably, the challenging 11-membered ring and bridged butenolide moieties in asteriscunolide D and 6,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad6c63d4d78af4bbfdb811c956c02d6d
https://doi.org/10.1021/ja5084927
https://doi.org/10.1021/ja5084927
Publikováno v:
Phytotherapy Research. 28:1577-1580
The present study aims to investigate the influence of irinotecan's toxicity by the biotransformation of glucoaurantio-obtusin to aurantio-obtusin. Intraperitoneal administration (i.p.) of 100 mg/kg aurantio-obtusin significantly increased the toxici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cd19b6ae5d450650f92d582fcad6dad
https://doi.org/10.1002/ptr.5162
https://doi.org/10.1002/ptr.5162