Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jonathan A. Reuven"'
Publikováno v:
European Journal of Organic Chemistry, 2022, Vol.2022(47) [Peer Reviewed Journal]
The iridium catalysed C−H borylation of polyfluorinated arenes and heteroarenes occurs rapidly and efficiently. As with other borylation reactions, whilst steric parameters dominate, an underlying electronic influence on reaction selectivity can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1afb28e69ca3319cdc893c7f97414d14
https://doi.org/10.1002/ejoc.202201005
https://doi.org/10.1002/ejoc.202201005
Publikováno v:
Tetrahedron, 2020, Vol.76(3), pp.29723 [Peer Reviewed Journal]
Regioselectively polysubstituted pyridines can be efficiently accessed from 2-halopyridines via a sequence involving C–H borylation, Suzuki-Miyaura cross-coupling and nucleophilic aromatic substitution chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::327341a970ab19f88b153fcbb6d2fefd
https://doi.org/10.1016/j.tet.2019.130836
https://doi.org/10.1016/j.tet.2019.130836
Autor:
Wang Yeuk Kong, Kathy Hiu Laam Po, Chun Wah Lo, Amaya Sirinimal, Sheng Chen, Xuechen Li, Jonathan Avraham Reuven, Ho Yin Lam, Chung Hei Lo, Kang Jin
Publikováno v:
Bioorganicmedicinal chemistry. 26(5)
Teixobactin is a structurally and mechanistically novel antimicrobial peptide with potent activities against Gram-positive pathogens. It contains l -allo-enduracididine (End) residue which is not readily accessible. In this report, we have used conve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42b4e457920f0b325d0c18aef6162a8e
https://pubmed.ncbi.nlm.nih.gov/29398444
https://pubmed.ncbi.nlm.nih.gov/29398444
Autor:
Xuechen Li, Sheng Chen, Ho Ting Lau, Ting Ho Chan, Kang Jin, Shengxi Wang, Kathy Hiu Laam Po, Chi Nga Wai, Jonathan Avraham Reuven
Publikováno v:
Bioorganicmedicinal chemistry. 25(18)
Convergent Ser/Thr ligation has been used to prepare a series of teixobactin analogues (28 in total) to establish a structure-activity relationship of teixobactin. anti-bacterial evaluations of these synthetic analogues have revealed the critical ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::440761649aa062f1744b37f61f66891c
https://pubmed.ncbi.nlm.nih.gov/28495382
https://pubmed.ncbi.nlm.nih.gov/28495382