Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Hsyueh Liang Wu"'
Publikováno v:
Frontiers in Chemistry, Vol 12 (2024)
Externí odkaz:
https://doaj.org/article/193770eaa5b444798ecd2035ce07753c
Autor:
Chien-Tien Chen, Yu-Chang Chang, Pin-Xuan Tseng, Chien-I Lein, Shiang-Fu Hung, Hsyueh-Liang Wu
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 1, p 513 (2022)
Several 2-substituted (H, Ph, and S-Me) and 1-substituted (H, Ph, and Bn), 3-hydroxy-1,3-quinazolin(di)ones were utilized for the first time as radical trapping agents in asymmetric 1,2-oxytrifluoromethylation of styrenes catalyzed by chiral vanadyl
Externí odkaz:
https://doaj.org/article/e48cbf2d189b40d4a752a606f6834af0
Autor:
Hung-Kai Wang, Yu-Lun Chio, Gangaram Pallikonda, Hsyueh-Liang Wu, Haw-Lih Su, Jen-Chieh Hsieh
Publikováno v:
Molecules, Vol 25, Iss 22, p 5303 (2020)
A synthetic approach to quinindoline derivatives by the Cu-catalyzed dual cyclization has been developed. This catalytic reaction is a practical method for the systematic synthesis of quinindoline core structure, which contains a limited-step synthet
Externí odkaz:
https://doaj.org/article/deed9d5d02954ed390970eb8af877d3c
Publikováno v:
The Chemical Record. 21:3954-3963
The development of efficient synthetic methods for accessing enantioenriched α-chiral amines is of great importance in the disciplines of medicinal and synthetic organic chemistry. Enantioselective Rh-catalyzed 1,2-addition reactions to activated im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb4f5ff15eb628c37cc2af62dfc6b9f3
https://doi.org/10.1002/tcr.202100209
https://doi.org/10.1002/tcr.202100209
Publikováno v:
Organometallics. 40:3370-3388
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b81179aca12bc7b7e88422ec54bb96f5
https://doi.org/10.1021/acs.organomet.1c00368
https://doi.org/10.1021/acs.organomet.1c00368
Publikováno v:
Organic & Biomolecular Chemistry. 18:2991-3006
The synthesis and properties of β-amino acids have drawn considerable attention owing to their ubiquitous presence in naturally occurring products of biological importance. While β3-amino acids can be readily prepared from α-amino acids via one-ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ab849131e8aa156f5512068b01bec7f
https://doi.org/10.1039/d0ob00448k
https://doi.org/10.1039/d0ob00448k
Publikováno v:
Organic Letters. 21:9468-9472
The asymmetric conjugate addition of arylboronic acids to N-phthalimidodehydroalanine 1i catalyzed by Rh(I)/L1a enables the facile preparation of chiral functionalized phenylalanines. The reaction proceeds by a conjugate addition and enantioselective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::456c569839f33b0eada61cf95742b12e
https://doi.org/10.1021/acs.orglett.9b03666
https://doi.org/10.1021/acs.orglett.9b03666
Autor:
Ming Kang Tsai, Julian P. Henschke, Balraj Gopula, Ting Shen Kuo, Ping Yu Wu, Hsyueh Liang Wu, Jia Hong Jian, Jin Fong Syu, Wei Sian Li, Meng Chi Hsieh
Publikováno v:
Organic Letters. 21:4614-4618
A chiral rhodium(I)-diene catalyst enabled the one-step synthesis of β-aryl β-imido sulfones under mild reaction conditions. By selection of the chiral diene ligand L1a or L2, each enantiomer of the chiral β-aryl β-imido sulfone target can be acc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e4c1b6927e9415754fe9da426bd1df
https://doi.org/10.1021/acs.orglett.9b01513
https://doi.org/10.1021/acs.orglett.9b01513
Publikováno v:
Organic letters. 23(3)
The 1-aryl tetrahydroisoquinolines (1-aryl THIQs) are omnipresent in biologically active molecules. Here we report on the direct asymmetric synthesis of these valuable compounds via the reaction of 3,4-dihydroisoquinolinium tetraarylborates. The dual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40043e33231280277e8886943f1d8564
https://pubmed.ncbi.nlm.nih.gov/33492973
https://pubmed.ncbi.nlm.nih.gov/33492973
Autor:
Yu Lun Chio, Haw-Lih Su, Jen-Chieh Hsieh, Hung Kai Wang, Gangaram Pallikonda, Hsyueh Liang Wu
Publikováno v:
Molecules
Volume 25
Issue 22
Molecules, Vol 25, Iss 5303, p 5303 (2020)
Volume 25
Issue 22
Molecules, Vol 25, Iss 5303, p 5303 (2020)
A synthetic approach to quinindoline derivatives by the Cu-catalyzed dual cyclization has been developed. This catalytic reaction is a practical method for the systematic synthesis of quinindoline core structure, which contains a limited-step synthet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::046b2cb17219bac442f473f5994a04e6
https://hdl.handle.net/10576/17896
https://hdl.handle.net/10576/17896
