Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Xihao Chang"'
Publikováno v:
Advanced Science, Vol 11, Iss 36, Pp n/a-n/a (2024)
Abstract The development of efficient methodologies for the controlled manufacture of specific stereoisomers bearing quaternary stereocenters has prompted advances in a variety of scientific disciplines including pharmaceutical chemistry, materials s
Externí odkaz:
https://doaj.org/article/3507284601924b5581f9fbdc839490b4
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
Asymmetric catalytic methods for the divergent construction of phosphoryl derivatives are not widely available. Here, the authors show nickel-catalyzed dienylation and enantioselective allenylation of phosphine oxides with high chemo-, regio-, and en
Externí odkaz:
https://doaj.org/article/47645b98af5b4db3826cba60f54a6880
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
Chiral acetylenic derivatives are found in many bioactive compounds and are versatile building blocks in organic synthesis. Here, the authors report a mild enantioselective nickel/Lewis acid-catalyzed asymmetric propargylic substitution reaction whic
Externí odkaz:
https://doaj.org/article/95457fe0465d451bbe506907cf00b536
Publikováno v:
Journal of Agricultural and Food Chemistry. 70:13839-13848
A series of pyrazol-5-yl-benzamide derivatives containing the oxazole group were designed and synthesized as potential SDH inhibitors. According to the results of the bioassays, most target compounds displayed moderate-to-excellent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8293d2cfd55fc8cd7dc22a976ace480
https://doi.org/10.1021/acs.jafc.2c04708
https://doi.org/10.1021/acs.jafc.2c04708
Publikováno v:
Journal of the American Chemical Society. 143:21048-21055
A highly enantioselective O-propargylation catalyzed by combining a phosphine-nickel complex and an axially chiral sodium dicarboxylate has been developed. The transformation features mild reaction conditions, a broad substrate scope, and excellent f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc48af10fda419200a4470acec0f2d87
https://doi.org/10.1021/jacs.1c11044
https://doi.org/10.1021/jacs.1c11044
Publikováno v:
Angewandte Chemie. 7/27/2020, Vol. 132 Issue 31, p12712-12722. 11p.
Publikováno v:
The Journal of Organic Chemistry. 86:16068-16076
An efficient and valuable N-N dimerization reaction of N-alkoxyamides is reported under undivided electrolytic conditions. This electrochemical strategy provides a powerful way to access a wide range of advanced, highly functionalized hydrazines. Rem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce6d3a39d90e640d860bda5de8a694f3
https://doi.org/10.1021/acs.joc.1c01294
https://doi.org/10.1021/acs.joc.1c01294
Publikováno v:
Angewandte Chemie International Edition. 59:18500-18504
An enantioselective bifunctional squaramide-catalyzed detrifluoroacetylative alkylation reaction has been developed under electrochemical conditions. The unified strategy based on this key tandem methodology has been divergently explored for the asym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::439ba5211a25745481d198f17008147c
https://doi.org/10.1002/anie.202006903
https://doi.org/10.1002/anie.202006903
Publikováno v:
The Journal of organic chemistry. 86(22)
An efficient and valuable N-N dimerization reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85826186d4b7956d9d19ef9a43d7b474
https://pubmed.ncbi.nlm.nih.gov/34464121
https://pubmed.ncbi.nlm.nih.gov/34464121
Publikováno v:
Organic Letters. 21:4915-4918
Asymmetric assembly of atropisomeric anilines from abundant and readily available precursors is one of the most challenging but valuable processes in organic synthesis. The use of highly efficient Smiles rearrangement to accomplish switchable enantio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe9692a7f1aa00ff408db9f8a93088b2
https://doi.org/10.1021/acs.orglett.9b01848
https://doi.org/10.1021/acs.orglett.9b01848