Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Xing-Wen Sun"'
Publikováno v:
Journal of Saudi Chemical Society, Vol 22, Iss 6, Pp 654-664 (2018)
An Efficient method for the syntheses of N-tert-butanesulfinyl aldimines in water was developed using Amberlyst-15 as catalyst. Subsequently, chiral homoallylic amines were synthesized in one pot from aldehydes by combining with In-promoted allylatio
Externí odkaz:
https://doaj.org/article/343df1b4cab040efb8b17d502784923f
Autor:
Yang Zong, Yan-Yan Xu, Yan Wu, Yamin Liu, Qian Li, Furong Lin, Shang-Bo Yu, Hui Wang, Wei Zhou, Xing-Wen Sun, Dan-Wei Zhang, Zhan-Ting Li
Publikováno v:
Journal of Materials Chemistry B. 10:3268-3276
Heparins are natural and partially degraded polyelectrolytes that consist of sulfated polysaccharide backbones. However, as clinically used anticoagulants, heparins are associated with clinical bleeding risks and thus require rapid neutralization. Pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08f81fe14190a8393844461c81be558d
https://doi.org/10.1039/d2tb00174h
https://doi.org/10.1039/d2tb00174h
Publikováno v:
The Journal of organic chemistry.
Highly enantioselective synthesis of 3,3'-spirooxindole γ-lactams with three contiguous stereocenters (two quaternary) was achieved. The aza-Michael/Mannich cascade reaction of α-imine-β-oxobutanamides and methyleneindolinones catalyzed by a bifun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ca54a1bbe489526aae3854b606c381a
https://pubmed.ncbi.nlm.nih.gov/35763038
https://pubmed.ncbi.nlm.nih.gov/35763038
Publikováno v:
ACS macro letters. 9(1)
Two metal porous organic polymers (POPs) that contain the [Ru(bpy)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b411917ffd6260ed131ffd69da703ee3
https://pubmed.ncbi.nlm.nih.gov/35638654
https://pubmed.ncbi.nlm.nih.gov/35638654
Publikováno v:
RSC advances. 12(25)
A novel approach to synthesize chiral 1,2-oxazinane spirocyclic scaffolds by organocatalytic [4 + 2] cycloaddition reaction between methyleneindolinones and γ-aminooxy-α,β-unsaturated ester has been disclosed. Furthermore, a hydrazide 1,4-synthon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2677cb54786623568c05c21ca1cdf84
https://pubmed.ncbi.nlm.nih.gov/35685709
https://pubmed.ncbi.nlm.nih.gov/35685709
Publikováno v:
Organicbiomolecular chemistry. 20(15)
Three kinds of diverse functionalized pyrrolo[2,3-b]indole derivatives are constructed respectively through a base-controlled dearomative [3 + 2] cycloaddition reaction between 3-nitroindoles and fumaric acid amide esters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed1b9b7532a94a3cd22c9763850d8698
https://pubmed.ncbi.nlm.nih.gov/35352074
https://pubmed.ncbi.nlm.nih.gov/35352074
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Publikováno v:
Organic Letters. 22:3351-3355
A simple, direct, and highly enantioselective synthesis of spiro-oxindole piperidin-2-one derivatives was achieved through an aza-Michael/Michael cyclization cascade sequence using a squaramide catalyst. The desired products were obtained in excellen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93ecbbb554c9b11ce75f5ea44a00d2dc
https://doi.org/10.1021/acs.orglett.0c00779
https://doi.org/10.1021/acs.orglett.0c00779
Publikováno v:
ACS Macro Letters. 9:90-95
Two metal porous organic polymers (POPs) that contain the [Ru(bpy)3]2+ cores are prepared via one-pot Suzuki–Miyaura coupling reactions. Both Ru-POPs are thermally stable at up to 340 °C in air and...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faf2c5cabfb9c6b8dd83e602c251290d
https://doi.org/10.1021/acsmacrolett.9b00872
https://doi.org/10.1021/acsmacrolett.9b00872
Publikováno v:
Green Chemistry. 22:136-143
Two rigid porous organic polymers (Ir-POP-1 and Ir-POP-2) were prepared from the coupling reactions of tetraphenylmethane tetraborate and two [Ir(ppy)2(dtbbpy)]+-based bitopic linkers and applied as heterogeneous visible-light photocatalysts for orga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::983be9e9e47361ee09ba75ba9ce738ab
https://doi.org/10.1039/c9gc03688a
https://doi.org/10.1039/c9gc03688a