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Refinado por: Base de dados/Biblioteca: Engineered Materials Abstracts remover Base de dados/Biblioteca: NUS Single-Journal Subscriptions remover
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1
Bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)tetrak is( mu 4-1,1,1,5,5,5-hexafluoropentane-2,2,4,4-tetraolato)copper(II)o ctatin(II): a prospective precursor for Cu-doped SnO2 films
Bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)tetrak is( mu 4-1,1,1,5,5,5-hexafluoropentane-2,2,4,4-tetraolato)copper(II)o ctatin(II): a prospective precursor for Cu-doped SnO2 films
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Bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)tetrak is( mu 4-1,1,1,5,5,5-hexafluoropentane-2,2,4,4-tetraolato)copper(II)o ctatin(II): a prospective precursor for Cu-doped SnO2 films

Lieberman, Craig M ; Filatov, Alexander S ; Vreshch, Volodimir D ; Dikarev, Evgeny V

Acta crystallographica. Section C, Crystal structure communications, 2013-12, Vol.69 (12), p.1427-1430 [Periódico revisado por pares]

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2
Recent advances in the synthesis of axially chiral biaryls via transition metal-catalysed asymmetric C-H functionalization
Recent advances in the synthesis of axially chiral biaryls via transition metal-catalysed asymmetric C-H functionalization
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Recent advances in the synthesis of axially chiral biaryls via transition metal-catalysed asymmetric C-H functionalization

Liao, Gang ; Zhou, Tao ; Yao, Qi-Jun ; Shi, Bing-Feng

Chemical communications (Cambridge, England), 2019-07, Vol.55 (59), p.8514-8523 [Periódico revisado por pares]

England: Royal Society of Chemistry

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3
Asymmetric total synthesis of prostaglandin C2 TBS ether
Asymmetric total synthesis of prostaglandin C2 TBS ether
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Asymmetric total synthesis of prostaglandin C2 TBS ether

Yi, Xiaofen ; Long, Xueyu ; Chen, Yu ; Cen, Xiangling ; Tang, Pei ; Chen, Fener

Chemical communications (Cambridge, England), 2022, Vol.58 (40), p.6000-6003 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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4
Catalytic asymmetric chemoselective 1,3-dipolar cycloadditions of an azomethine ylide with isatin-derived imines: diastereo- and enantioselective construction of a spiro[imidazolidine-2,3'-oxindole] framework
Catalytic asymmetric chemoselective 1,3-dipolar cycloadditions of an azomethine ylide with isatin-derived imines: diastereo- and enantioselective construction of a spiro[imidazolidine-2,3'-oxindole] framework
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Catalytic asymmetric chemoselective 1,3-dipolar cycloadditions of an azomethine ylide with isatin-derived imines: diastereo- and enantioselective construction of a spiro[imidazolidine-2,3'-oxindole] framework

Wang, Yue-Ming ; Zhang, Hong-Hao ; Li, Can ; Fan, Tao ; Shi, Feng

Chemical communications (Cambridge, England), 2016-01, Vol.52 (9), p.1804-1807 [Periódico revisado por pares]

England

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5
Pyrazolone: a powerful synthon for asymmetric diverse derivatizations
Pyrazolone: a powerful synthon for asymmetric diverse derivatizations
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Pyrazolone: a powerful synthon for asymmetric diverse derivatizations

Liu, Siyuan ; Bao, Xiaoze ; Wang, Baomin

Chemical communications (Cambridge, England), 2018-10, Vol.54 (82), p.11515-11529 [Periódico revisado por pares]

England: Royal Society of Chemistry

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6
Three-dimensional capillary ratchet-induced liquid directional steering
Three-dimensional capillary ratchet-induced liquid directional steering
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Three-dimensional capillary ratchet-induced liquid directional steering

Feng, Shile ; Zhu, Pingan ; Zheng, Huanxi ; Zhan, Haiyang ; Chen, Chen ; Li, Jiaqian ; Wang, Liqiu ; Yao, Xi ; Liu, Yahua ; Wang, Zuankai

Science (American Association for the Advancement of Science), 2021-09, Vol.373 (6561), p.1344-1348 [Periódico revisado por pares]

United States: The American Association for the Advancement of Science

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7
Chiral N,N'-dioxide-Sc(NTf 2 ) 3 complex-catalyzed asymmetric bromoamination of chalones with N-bromosuccinimide as both bromine and amide source
Chiral N,N'-dioxide-Sc(NTf 2 ) 3 complex-catalyzed asymmetric bromoamination of chalones with N-bromosuccinimide as both bromine and amide source
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Chiral N,N'-dioxide-Sc(NTf 2 ) 3 complex-catalyzed asymmetric bromoamination of chalones with N-bromosuccinimide as both bromine and amide source

Wang, Zhengmeng ; Lin, Lili ; Zhou, Pengfei ; Liu, Xiaohua ; Feng, Xiaoming

Chemical communications (Cambridge, England), 2017-03, Vol.53 (24), p.3462-3465 [Periódico revisado por pares]

England

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8
Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives
Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives
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Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives

Chauhan, Pankaj ; Mahajan, Suruchi ; Enders, Dieter

Chemical communications (Cambridge, England), 2015-08, Vol.51 (65), p.1289-1297 [Periódico revisado por pares]

England

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9
Metastable Dion-Jacobson 2D structure enables efficient and stable perovskite solar cells
Metastable Dion-Jacobson 2D structure enables efficient and stable perovskite solar cells
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Metastable Dion-Jacobson 2D structure enables efficient and stable perovskite solar cells

Zhang, Fei ; Park, So Yeon ; Yao, Canglang ; Lu, Haipeng ; Dunfield, Sean P ; Xiao, Chuanxiao ; Uličná, Soňa ; Zhao, Xiaoming ; Du Hill, Linze ; Chen, Xihan ; Wang, Xiaoming ; Mundt, Laura E ; Stone, Kevin H ; Schelhas, Laura T ; Teeter, Glenn ; Parkin, Sean ; Ratcliff, Erin L ; Loo, Yueh-Lin ; Berry, Joseph J ; Beard, Matthew C ; Yan, Yanfa ; Larson, Bryon W ; Zhu, Kai

Science (American Association for the Advancement of Science), 2022-01, Vol.375 (6576), p.71-76 [Periódico revisado por pares]

United States: The American Association for the Advancement of Science

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10
Comment on “Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence”
Comment on “Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence”
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Comment on “Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence”

Sherman, David H. ; Tsukamoto, Sachiko ; Williams, Robert M.

Science (American Association for the Advancement of Science), 2015-07, Vol.349 (6244), p.149-149 [Periódico revisado por pares]

Washington: The American Association for the Advancement of Science

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