Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Ren Rong Liu"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-8 (2024)
Abstract Developing facile and direct synthesis routes for enantioselective construction of cyclic π-conjugated molecules is crucial. However, originate chirality from the distorted structure around heptagon-containing polyarenes is largely overlook
Externí odkaz:
https://doaj.org/article/6f94e0acd67941e8a534289991e8beb8
Publikováno v:
Chinese Journal of Chemistry; Apr2024, Vol. 42 Issue 7, p711-718, 8p
Publikováno v:
ACS Catalysis. :7680-7690
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9e6946c46a7428616d441aa5c83c0fc
https://doi.org/10.1021/acscatal.3c00732
https://doi.org/10.1021/acscatal.3c00732
Publikováno v:
Chemical Science. 14:3346-3351
The palladium-catalyzed rearrangement of VCPs (dienyl or trienyl cyclopropanes) for the construction of functionalized cyclopentene units was reported in high yields and with excellent regioselectivities and enantioselectivities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b61e96a52eb69fcd5db2dff899785c47
https://doi.org/10.1039/d2sc06548g
https://doi.org/10.1039/d2sc06548g
Publikováno v:
Organic Letters. 24:6148-6153
Despite the great advancement in atroposelective synthesis in the past decades, the enantioselective synthesis of 2,2'-difluoro-1-biaryls is unprecedented. Herein, a palladium and chiral amino acid catalyzed atroposelective C-H olefination to constru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdf7e045864a885bfcc6751f8079b4ac
https://doi.org/10.1021/acs.orglett.2c02303
https://doi.org/10.1021/acs.orglett.2c02303
Publikováno v:
Angewandte Chemie. 135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18bd25f9c4086359f825ff2d72237732
https://doi.org/10.1002/ange.202218871
https://doi.org/10.1002/ange.202218871
Publikováno v:
Synlett. 33:1589-1595
Benzimidazole atropisomers bearing a C–N axis are privileged structural frameworks in pharmaceutical and natural products, thus appealing an increasing interest for its asymmetric synthesis. Here, we briefly discuss recent advances in the asymmetri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a059de48dfa88d3d5c0acd1688a14998
https://doi.org/10.1055/a-1833-8979
https://doi.org/10.1055/a-1833-8979
Publikováno v:
Angewandte Chemie. 133:21886-21890
N-C Biaryl atropisomers are prevalent in natural products and bioactive drug molecules. However, the enantioselective synthesis of such molecules has not developed significantly. Particularly, the enantioselective synthesis of N-C biaryl atropisomers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::590f4a689ea31a2985520f8168701726
https://doi.org/10.1002/ange.202108747
https://doi.org/10.1002/ange.202108747
Publikováno v:
Angewandte Chemie (International ed. in English). 61(49)
Diarylamines and related scaffolds are ubiquitous atropisomeric chemotypes in biologically active natural products. However, the catalytic asymmetric synthesis of these axially chiral compounds remains largely unexplored. Herein, we report that a BIN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::559d16cef422b9c5370099361b3e8d28
https://pubmed.ncbi.nlm.nih.gov/36220781
https://pubmed.ncbi.nlm.nih.gov/36220781
Publikováno v:
Angewandte Chemie (International ed. in English). 61(44)
N-N Atropisomers are a common motif in natural products and represent a significant dimension for exploration in modern pharmaceutical and medicinal chemistry. However, the catalytic atroposelective synthesis of such molecules remains challenging, ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15c646d0d3c688c851478487388790c1
https://pubmed.ncbi.nlm.nih.gov/36104869
https://pubmed.ncbi.nlm.nih.gov/36104869