Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Day-Shin Hsu"'
Publikováno v:
Organic Letters. 22:6252-6256
A novel and efficient reductive N-alkenylation of iminoquinones with electron-deficient olefins has been successfully developed by Pd(II)-catalyzed redox-neutral reactions, which provides a synthes...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfe4bd674379c1e1b8e666bcb2a3b9d4
https://doi.org/10.1021/acs.orglett.0c01929
https://doi.org/10.1021/acs.orglett.0c01929
Autor:
Day‐Shin Hsu, Tai‐Yun Hwang
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4120912558efb74fb70eed14790ae372
https://doi.org/10.1002/slct.202103794
https://doi.org/10.1002/slct.202103794
Publikováno v:
The Journal of organic chemistry. 87(1)
The asymmetric total syntheses of (+)-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11fe6c9617b80eb6d7691624661c7c36
https://pubmed.ncbi.nlm.nih.gov/34949087
https://pubmed.ncbi.nlm.nih.gov/34949087
Publikováno v:
Organic letters. 22(16)
A novel and efficient reductive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb7ed2fb3718c774cef746cbcffb1ba6
https://pubmed.ncbi.nlm.nih.gov/32692563
https://pubmed.ncbi.nlm.nih.gov/32692563
Autor:
Day‐Shin Hsu, Tai‐Yu Hwang
Publikováno v:
European Journal of Organic Chemistry. 2018:4689-4695
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8d556a329736a0cd5668ff0545d1f78
https://doi.org/10.1002/ejoc.201800806
https://doi.org/10.1002/ejoc.201800806
Publikováno v:
Journal of Organic Chemistry; 1/7/2022, Vol. 87 Issue 1, p644-651, 8p
Autor:
Day-Shin Hsu, Suz-Ping Liang
Publikováno v:
The Journal of organic chemistry. 85(2)
A general and efficient method for the synthesis of tricyclic spirocarbocycles is described. Various cyclic enal-enones were reacted with an N-heterocyclic carbene, and an intramolecular Stetter reaction proceeded smoothly to give various tricyclic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8c48cb2ec28d0c8112b85a54cb362a1
https://pubmed.ncbi.nlm.nih.gov/31794214
https://pubmed.ncbi.nlm.nih.gov/31794214
Autor:
Jiun-Yi Huang, Day-Shin Hsu
Publikováno v:
Organic letters. 21(18)
The first total syntheses of (±)-parimycin and (R)-parimycin were accomplished from O-methylnaphthazarin (6) in nine synthetic steps. Intermolecular Diels–Alder reaction of 6 with diene 7, cyclodehydrogenation catalyzed by iodine-dimethyl sulfoxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::341e3a47db1ae09e75c850d0e059dcc2
https://pubmed.ncbi.nlm.nih.gov/31512884
https://pubmed.ncbi.nlm.nih.gov/31512884
Autor:
Day-Shin Hsu, Chiao-Yun Cheng
Publikováno v:
The Journal of organic chemistry. 84(17)
Various benzaldehyde tethers with a cyclic enone were prepared from commercially available 2-hydroxybenzaldehydes via a three-step sequence involving triflate formation, Sonogashira cross-coupling, and regioselective hydrogenation. These substrates w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9179bc90e17307717d3d9f7ff6f77d0b
https://pubmed.ncbi.nlm.nih.gov/31397574
https://pubmed.ncbi.nlm.nih.gov/31397574
Publikováno v:
Organic & Biomolecular Chemistry. 14:2306-2317
Multicomponent reactions of phosphines, enynedioates and benzylidene malononitriles provide highly substituted syn-selective cyclopentenes appending the phosphorus ylide moiety in good yield with a diastereoselectivity of up to 100% through resonance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65405e1e97ac0592d8fa193b439ec34b
https://doi.org/10.1039/c5ob02445e
https://doi.org/10.1039/c5ob02445e