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Refinado por: Nome da Publicação: European Journal Of Organic Chemistry remover assunto: Physical Sciences remover
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1
Asymmetric Synthesis of Bispiro[γ‐butyrolactone‐pyrrolidin‐4,4′‐pyrazolone] Scaffolds Containing Two Quaternary Spirocenters via an Organocatalytic 1,3‐Dipolar Cycloaddition
Asymmetric Synthesis of Bispiro[γ‐butyrolactone‐pyrrolidin‐4,4′‐pyrazolone] Scaffolds Containing Two Quaternary Spirocenters via an Organocatalytic 1,3‐Dipolar Cycloaddition
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Asymmetric Synthesis of Bispiro[γ‐butyrolactone‐pyrrolidin‐4,4′‐pyrazolone] Scaffolds Containing Two Quaternary Spirocenters via an Organocatalytic 1,3‐Dipolar Cycloaddition

Chen, Nannan ; Zhu, Liping ; Gan, Lu ; Liu, Zhenquan ; Wang, Rui ; Cai, Xiaoqing ; Jiang, Xianxing

European journal of organic chemistry, 2018-06, Vol.2018 (23), p.2939-2943 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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2
Metal-Free Oxidative Carbon-Heteroatom Bond Formation Through C-H Bond Functionalization
Metal-Free Oxidative Carbon-Heteroatom Bond Formation Through C-H Bond Functionalization
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Metal-Free Oxidative Carbon-Heteroatom Bond Formation Through C-H Bond Functionalization

Samanta, Rajarshi ; Matcha, Kiran ; Antonchick, Andrey P.

European journal of organic chemistry, 2013-09, Vol.2013 (26), p.5769-5804 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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3
Biocatalyzed Enantioselective Reduction of Activated C=C Bonds: Synthesis of Enantiomerically Enriched α-Halo-β-arylpropionic Acids
Biocatalyzed Enantioselective Reduction of Activated C=C Bonds: Synthesis of Enantiomerically Enriched α-Halo-β-arylpropionic Acids
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Biocatalyzed Enantioselective Reduction of Activated C=C Bonds: Synthesis of Enantiomerically Enriched α-Halo-β-arylpropionic Acids

Brenna, Elisabetta ; Gatti, Francesco G. ; Manfredi, Alessia ; Monti, Daniela ; Parmeggiani, Fabio

European Journal of Organic Chemistry, 2011-07, Vol.2011 (20-21), p.4015-4022 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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4
One‐Pot l‐Proline‐Mediated Stereoselective α‐C(sp2)–H Fluorination of α,β‐Unsaturated Aldehydes through Methoxyfluorination–Elimination
One‐Pot l‐Proline‐Mediated Stereoselective α‐C(sp2)–H Fluorination of α,β‐Unsaturated Aldehydes through Methoxyfluorination–Elimination
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One‐Pot l‐Proline‐Mediated Stereoselective α‐C(sp2)–H Fluorination of α,β‐Unsaturated Aldehydes through Methoxyfluorination–Elimination

Zhou, Jiadi ; Jiang, Xinpeng ; Jin, Can ; Guo, Zhicheng ; Su, Bin ; Su, Weike

European journal of organic chemistry, 2017-07, Vol.2017 (25), p.3631-3634 [Periódico revisado por pares]

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5
Enantioselective Synthesis of trans‐2,3‐Dihydro‐1H‐indoles Through C–H Insertion of α‐Diazocarbonyl Compounds
Enantioselective Synthesis of trans‐2,3‐Dihydro‐1H‐indoles Through C–H Insertion of α‐Diazocarbonyl Compounds
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Enantioselective Synthesis of trans‐2,3‐Dihydro‐1H‐indoles Through C–H Insertion of α‐Diazocarbonyl Compounds

Santi, Micol ; Müller, Simon T. R. ; Folgueiras‐Amador, Ana A. ; Uttry, Alexander ; Hellier, Paul ; Wirth, Thomas

European journal of organic chemistry, 2017-04, Vol.2017 (14), p.1889-1893 [Periódico revisado por pares]

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6
Rhodium-Catalyzed Vinylic C-H Functionalization of Enol Carbamates with Maleimides
Rhodium-Catalyzed Vinylic C-H Functionalization of Enol Carbamates with Maleimides
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Rhodium-Catalyzed Vinylic C-H Functionalization of Enol Carbamates with Maleimides

Sharma, Satyasheel ; Han, Sang Hoon ; Jo, Hyeim ; Han, Sangil ; Mishra, Neeraj Kumar ; Choi, Miji ; Jeong, Taejoo ; Park, Jihye ; Kim, In Su

European journal of organic chemistry, 2016-07, Vol.2016 (21), p.3611-3618 [Periódico revisado por pares]

Weinheim: Blackwell Publishing Ltd

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7
Diastereoselective Hydrolysis of Branched Malonate Diesters by Porcine Liver Esterase: Synthesis of 5‐Benzyl‐Substituted Cα‐Methyl‐β‐proline and Catalytic Evaluation
Diastereoselective Hydrolysis of Branched Malonate Diesters by Porcine Liver Esterase: Synthesis of 5‐Benzyl‐Substituted Cα‐Methyl‐β‐proline and Catalytic Evaluation
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Diastereoselective Hydrolysis of Branched Malonate Diesters by Porcine Liver Esterase: Synthesis of 5‐Benzyl‐Substituted Cα‐Methyl‐β‐proline and Catalytic Evaluation

Kotapati, Hari Kiran ; Robinson, Jamarii D. ; Lawrence, Daniel R. ; Fortner, Kimberly R. ; Stanford, Caleb W. ; Powell, Douglas R. ; Wardenga, Rainer ; Bornscheuer, Uwe T. ; Masterson, Douglas S.

European journal of organic chemistry, 2017-05, Vol.2017 (20), p.3009-3016 [Periódico revisado por pares]

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8
Direct C-3-Arylations of 1H-Indazoles
Direct C-3-Arylations of 1H-Indazoles
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Direct C-3-Arylations of 1H-Indazoles

Ben-Yahia, Ali ; Naas, Mohammed ; El Kazzouli, Saïd ; Essassi, El Mokhtar ; Guillaumet, Gérald

European journal of organic chemistry, 2012-12, Vol.2012 (36), p.7075-7081 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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9
Synthesis, Skeletal Rearrangement, and Biological Activities of Spirooxindoles: Exploration of a Stepwise C-Piancatelli Rearrangement
Synthesis, Skeletal Rearrangement, and Biological Activities of Spirooxindoles: Exploration of a Stepwise C-Piancatelli Rearrangement
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Synthesis, Skeletal Rearrangement, and Biological Activities of Spirooxindoles: Exploration of a Stepwise C-Piancatelli Rearrangement

Huang, Li ; Zhang, Xiaoyu ; Li, Jing ; Ding, Ke ; Li, Xuehui ; Zheng, Wenxu ; Yin, Biaolin

European journal of organic chemistry, 2014-01, Vol.2014 (2), p.338-349 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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10
syn/anti Switching by Specific Heteroatom-Titanium Coordination in the Mannich-Like Synthesis of 2,3-Diaryl-β-amino Acid Derivatives
syn/anti Switching by Specific Heteroatom-Titanium Coordination in the Mannich-Like Synthesis of 2,3-Diaryl-β-amino Acid Derivatives
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syn/anti Switching by Specific Heteroatom-Titanium Coordination in the Mannich-Like Synthesis of 2,3-Diaryl-β-amino Acid Derivatives

Bonetti, Andrea ; Clerici, Francesca ; Foschi, Francesca ; Nava, Donatella ; Pellegrino, Sara ; Penso, Michele ; Soave, Raffaella ; Gelmi, Maria Luisa

European journal of organic chemistry, 2014-05, Vol.2014 (15), p.3203-3209 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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