Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Guolan Xiao"'
Autor:
Ruoqian Xie, Wanlu Li, Yuhua Ge, Yutong Zhou, Guolan Xiao, Qin Zhao, Yunxi Han, Yangyan Li, Gang Chen
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Chemically modified nucleosi(ti)des and functional oligonucleotides (ONs, including therapeutic oligonucleotides, aptamer, nuclease, etc.) have been identified playing an essential role in the areas of medicinal chemistry, chemical biology,
Externí odkaz:
https://doaj.org/article/afefdf79f32e446a97b557179516f069
Publikováno v:
Handbook of CH‐Functionalization. :1-65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40ee49e81e873bfe897e1ee6dce4b929
https://doi.org/10.1002/9783527834242.chf0217
https://doi.org/10.1002/9783527834242.chf0217
Publikováno v:
RSC Advances. 12:24930-24934
The palladium-catalyzed oxidative C-H olefinations of uridine, deoxyuridine, uridine monophosphate and uridine analogues are reported herein. This protocol provides an efficient, atom-economic and environmentally friendly approach to the synthesis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d585dafada38f4564f685b0070edd4d
https://doi.org/10.1039/d2ra03681a
https://doi.org/10.1039/d2ra03681a
Publikováno v:
CCS Chemistry. 2:432-439
Enantioenriched γ-butenolides are valuable structural cores in many pharmaceuticals and natural products, but their direct and catalytically asymmetric assembly remains rare. Here, we report an eff...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ee111b6a3c8fd347731dd52e24cd5dd
https://doi.org/10.31635/ccschem.020.201900089
https://doi.org/10.31635/ccschem.020.201900089
Publikováno v:
Advanced Synthesis & Catalysis. 362:1961-1965
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3fc43aca4a36fee13580ea87d998fbd
https://doi.org/10.1002/adsc.202000193
https://doi.org/10.1002/adsc.202000193
Publikováno v:
Organic Letters. 20:4531-4535
An asymmetric strategy for the construction of chiral sulfur-containing spirooxindole-fused heterocycles was achieved via a rhodium(II)/chiral phosphoric acid-cocatalyzed reaction between 2-mercaptophenyl ketones and 3-diazooxindoles. With this metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4a3c629c5a4c247c9d899e6ebbdefd0
https://doi.org/10.1021/acs.orglett.8b01833
https://doi.org/10.1021/acs.orglett.8b01833
Publikováno v:
The Journal of Organic Chemistry. 83:4786-4791
A facile method for the synthesis of γ-sulfur-substituted ketones is developed via a Rh(II)/Sc(III) cocatalyzed three-component reaction of diazo compounds with thiophenols and enones. With this method, different γ-sulfur-substituted ketones were o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e4177dcb763b1fca4f5bc61413b33a
https://doi.org/10.1021/acs.joc.7b03074
https://doi.org/10.1021/acs.joc.7b03074
Publikováno v:
Organic letters. 18(23)
An enantioselective method for the synthesis of α-mercapto-β-amino esters has been developed via a rhodium(II)/chiral phosphoric acid-cocatalyzed three-component reaction of diazo compounds, thiols, and imines. This transformation is proposed to pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a5c4ae1451ced32ada8cd1df6cd3a35
https://pubmed.ncbi.nlm.nih.gov/27934335
https://pubmed.ncbi.nlm.nih.gov/27934335
Publikováno v:
ChemInform. 46
A variety of di-ortho-substituted aryl bromides and some analogues is treated with acyclic secondary alkyl boronic acids in the presence of the efficient ligands (I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e7625caa0c17b41bc8ac8cfae0bd94d
https://doi.org/10.1002/chin.201531092
https://doi.org/10.1002/chin.201531092
Publikováno v:
Angewandte Chemie (International ed. in English). 54(12)
Bulky P,P=O ligands were designed to inhibit isomerization and reduction side reactions during the cross coupling between sterically hindered aryl halides and alkylboronic acids. Suzuki-Miyaura cross-couplings between di-ortho-substituted aryl bromid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb429fc5c6a7d6446a8fce9fd779c23
https://pubmed.ncbi.nlm.nih.gov/25630668
https://pubmed.ncbi.nlm.nih.gov/25630668