Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Toyoharu Kobayashi"'
Publikováno v:
Angewandte Chemie International Edition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e1eab241502c0e502095ddfcd2fa5a7
https://doi.org/10.1002/anie.202304132
https://doi.org/10.1002/anie.202304132
Publikováno v:
Organic Letters. 23:6916-6918
The first enantioselective total synthesis of tricyclic diterpenoid callilongisin B, which was isolated from Callicarpa longissima, has been achieved. The synthetic method includes a diastereoselective 1,4-addition and Hosomi-Sakurai allylation follo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbf279374dabe5ae72ddc71bf9d8a1f4
https://doi.org/10.1021/acs.orglett.1c02473
https://doi.org/10.1021/acs.orglett.1c02473
Publikováno v:
Organic Letters. 22:7609-7612
Mollebenzylanol A is a tyrosine phosphatase 1B inhibitor isolated from the leaves of Rhododendron molle in 2018 that has a highly functionalized structure. The first enantioselective total synthesi...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8b769751e3a313a65d6fb9a6a719afc
https://doi.org/10.1021/acs.orglett.0c02811
https://doi.org/10.1021/acs.orglett.0c02811
Publikováno v:
European Journal of Organic Chemistry. 2020:4050-4058
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::052be591995659e42d825b9956cb523f
https://doi.org/10.1002/ejoc.202000579
https://doi.org/10.1002/ejoc.202000579
Publikováno v:
Organic & Biomolecular Chemistry. 18:7316-7320
The first asymmetric total synthesis of isolinearol has been achieved with high stereoselectively. The synthetic method includes enatio- and diastereoselective reductive desymmetrization, stereocontrolled introduction of the methallyl group, regio- a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8bdc87e36449c66ac2e56418a9914f9
https://doi.org/10.1039/d0ob01430c
https://doi.org/10.1039/d0ob01430c
Publikováno v:
Organic letters. 23(18)
The enantioselective total synthesis of nesteretal A was achieved in 15 steps via biomimetic cascade hemiacetalizations at the final key step. Other key features of the total synthesis include Sharpless asymmetric dihydroxylation, diastereoselective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f81d2b948cedfb4c1641f3d5ffc423be
https://pubmed.ncbi.nlm.nih.gov/34449231
https://pubmed.ncbi.nlm.nih.gov/34449231
Publikováno v:
Organic letters. 23(17)
The first enantioselective total synthesis of tricyclic diterpenoid callilongisin B, which was isolated from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33451961ec493fa4bd3b00e821d35e46
https://pubmed.ncbi.nlm.nih.gov/34424723
https://pubmed.ncbi.nlm.nih.gov/34424723
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 77:1086-1095
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::316214fa51bd03ff236aa5258b408d72
https://doi.org/10.5059/yukigoseikyokaishi.77.1086
https://doi.org/10.5059/yukigoseikyokaishi.77.1086
Publikováno v:
Tetrahedron Letters. 60:2059-2062
The first total synthesis of tricyclic humulanolide wilfolide B was achieved. The synthetic strategy involved: i) radical cyclization with samarium(II) iodide to construct the bicyclic lactone from an acyclic compound, and ii) ring-closing metathesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b13ef7c239ddb586d30d1637c8bdbec
https://doi.org/10.1016/j.tetlet.2019.06.058
https://doi.org/10.1016/j.tetlet.2019.06.058
Autor:
Hideki Abe, Toyoharu Kobayashi, Ayumu Shinobe, Iori Takizawa, Hisanaka Ito, Yuichiro Kawamoto
Publikováno v:
Organic Letters. 21:3008-3012
A novel chiral 1,3-diketone possessing C2 symmetry was synthesized and utilized in the asymmetric synthesis of guignardone H and I by employing sequential condensation-6π-electrocyclization reactions with the novel 1,3-diketone followed by stereosel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a2b6911b8191904b9b232a63c205c56
https://doi.org/10.1021/acs.orglett.9b00486
https://doi.org/10.1021/acs.orglett.9b00486