Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Xiongda Xie"'
Publikováno v:
Advanced Science, Vol 11, Iss 14, Pp n/a-n/a (2024)
Abstract A robust and practical difluoroalkylation synthon, α,α‐difluoroenol species, which generated in situ from trifluoromethyl diazo compounds and water in the presence of dirhodium complex, is disclosed. As compared to the presynthesized dif
Externí odkaz:
https://doaj.org/article/24be90e74b9d43fd84634a71cc1b5cb1
Autor:
Shanliang Dong, Kemiao Hong, Zhijing Zhang, Jingjing Huang, Xiongda Xie, Haoxuan Yuan, Wenhao Hu, Xinfang Xu
Publikováno v:
Angewandte Chemie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3acfb926f7ea740bf4833464e29962ff
https://doi.org/10.1002/ange.202302371
https://doi.org/10.1002/ange.202302371
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af4466015a54957562407ba270441fb
https://doi.org/10.1002/chem.202300140
https://doi.org/10.1002/chem.202300140
Publikováno v:
Organic Chemistry Frontiers. 9:2102-2108
An asymmetric three-component reaction via Mannich-type interception of an oxonium ylide with a 7-membered imine has been disclosed, providing chiral dibenzoazepine analogues with excellent stereoselectivity and structural diversity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf9ab2e1212b1544b5c8fd64d9c30f89
https://doi.org/10.1039/d2qo00076h
https://doi.org/10.1039/d2qo00076h
Publikováno v:
Molecular Diversity.
A gold-catalyzed carbocyclization/imidization cascade reaction has been developed,leading a facile access to the synthesis of functionalized nitrones in moderate to good yields under mild conditions. The reaction initiated by a catalytic 6-endo-dig d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a9612656d35ce1bec24e933a2b46d83
https://doi.org/10.1007/s11030-022-10530-5
https://doi.org/10.1007/s11030-022-10530-5
Publikováno v:
Synlett. 32:1957-1962
A mild and facile synthetic method via convergent assembly of two reactive intermediates generated in situ has been developed. This method provides an efficient way to construct six- and seven-membered N-heterocycles containing a biaryl linkage. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cb990e3493839df10171812921422df
https://doi.org/10.1055/a-1623-1490
https://doi.org/10.1055/a-1623-1490
Publikováno v:
Advanced Synthesis & Catalysis. 363:4018-4023
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::523502f377f3992abefd0031013dee73
https://doi.org/10.1002/adsc.202100602
https://doi.org/10.1002/adsc.202100602
Publikováno v:
Chemical Communications. 57:12171-12174
An efficient gold and chiral phosphoric acid cooperatively catalyzed enantioselective oxidative cyclization/Mannich-type addition reaction of homopropargyl amides with nitrones has been developed, which provides chiral pyrrolidin-3-ones in high yield
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::093a1240d61177e13ee201702e9f2c17
https://doi.org/10.1039/d1cc04830a
https://doi.org/10.1039/d1cc04830a
Publikováno v:
Organicbiomolecular chemistry. 20(22)
A diastereoselective aldol-type interception of phenolic oxonium ylides with isatins provides an effective access to 2,2-disubstituted dihydrobenzofuran derivatives in high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f56a74a48cdf1126b1b7d96144366330
https://pubmed.ncbi.nlm.nih.gov/35611674
https://pubmed.ncbi.nlm.nih.gov/35611674
Publikováno v:
Angewandte Chemie International Edition. 60:1992-1999
An unprecedented catalytic asymmetric allylation of isatins and isatin-derived ketimines is reported enabled by a gold and chiral organocatalyst cooperative catalysis strategy. This method offers expeditious access to chiral 2,5-disubsituted alkylide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::816e3c583688063e36d108e55d7c6a32
https://doi.org/10.1002/anie.202012678
https://doi.org/10.1002/anie.202012678