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Refinado por: Nome da Publicação: Chemistry : A European Journal remover assunto: Physical Sciences remover
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1
Aldolase Antibody Activation of Prodrugs of Potent Aldehyde-Containing Cytotoxics for Selective Chemotherapy
Aldolase Antibody Activation of Prodrugs of Potent Aldehyde-Containing Cytotoxics for Selective Chemotherapy
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Aldolase Antibody Activation of Prodrugs of Potent Aldehyde-Containing Cytotoxics for Selective Chemotherapy

Sinha, Subhash C. ; Li, Lian-Sheng ; Watanabe, Shin-ichi ; Kaltgrad, Eiton ; Tanaka, Fujie ; Rader, Christoph ; Lerner, Richard A. ; Barbas III, Carlos F.

Chemistry : a European journal, 2004-10, Vol.10 (21), p.5467-5472 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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2
Enantioselective Total Synthesis of Some Brevicomins Using Aldolase Antibody 38C2
Enantioselective Total Synthesis of Some Brevicomins Using Aldolase Antibody 38C2
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Enantioselective Total Synthesis of Some Brevicomins Using Aldolase Antibody 38C2

List, Benjamin ; Shabat, Doron ; Barbas III, Carlos F. ; Lerner, Richard A.

Chemistry : a European journal, 1998-05, Vol.4 (5), p.881-885 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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3
Last-Step Enzymatic [18F]-Fluorination of Cysteine-Tethered RGD Peptides Using Modified Barbas Linkers
Last-Step Enzymatic [18F]-Fluorination of Cysteine-Tethered RGD Peptides Using Modified Barbas Linkers
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Last-Step Enzymatic [18F]-Fluorination of Cysteine-Tethered RGD Peptides Using Modified Barbas Linkers

Zhang, Qingzhi ; Dall'Angelo, Sergio ; Fleming, Ian N. ; Schweiger, Lutz F. ; Zanda, Matteo ; O'Hagan, David

Chemistry : a European journal, 2016-07, Vol.22 (31), p.10998-11004 [Periódico revisado por pares]

Germany: Blackwell Publishing Ltd

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4
Direct Catalytic Asymmetric Synthesis of Highly Functionalized 2‐Methylchroman‐2,4‐diols via Barbas–List Aldol Reaction
Direct Catalytic Asymmetric Synthesis of Highly Functionalized 2‐Methylchroman‐2,4‐diols via Barbas–List Aldol Reaction
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Direct Catalytic Asymmetric Synthesis of Highly Functionalized 2‐Methylchroman‐2,4‐diols via Barbas–List Aldol Reaction

Ramachary, Dhevalapally B. ; Sakthidevi, Rajasekar

Chemistry : a European journal, 2009-04, Vol.15 (18), p.4516-4522 [Periódico revisado por pares]

Weinheim: WILEY‐VCH Verlag

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5
Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles
Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles
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Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles

Tan, Bin ; Zeng, Xiaofei ; Leong, Wendy Wen Yi ; Shi, Zugui ; Barbas III, Carlos F. ; Zhong, Guofu

Chemistry : a European journal, 2012-01, Vol.18 (1), p.63-67 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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6
Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion[1]
Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion[1]
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Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion[1]

Subirós-Funosas, Ramon ; Prohens, Rafel ; Barbas, Rafael ; El-Faham, Ayman ; Albericio, Fernando

Chemistry : a European journal, 2009-09, Vol.15 (37), p.9394-9403 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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7
Aminocatalytic Cross-Coupling Approach via Iminium Ions to Different CC Bonds
Aminocatalytic Cross-Coupling Approach via Iminium Ions to Different CC Bonds
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Aminocatalytic Cross-Coupling Approach via Iminium Ions to Different CC Bonds

Mupparapu, Nagaraju ; Battini, Narsaiah ; Battula, Satyanarayana ; Khan, Shahnawaz ; Vishwakarma, Ram A ; Ahmed, Qazi Naveed

Chemistry : a European journal, 2015-02, Vol.21 (7), p.2954-2960 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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8
Fluorinated Aromatic Ketones as Nucleophiles in the Asymmetric Organocatalytic Formation of CC and CN Bonds: A Facile Route to the Construction of Fluorinated Quaternary Stereogenic Centers
Fluorinated Aromatic Ketones as Nucleophiles in the Asymmetric Organocatalytic Formation of CC and CN Bonds: A Facile Route to the Construction of Fluorinated Quaternary Stereogenic Centers
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Fluorinated Aromatic Ketones as Nucleophiles in the Asymmetric Organocatalytic Formation of CC and CN Bonds: A Facile Route to the Construction of Fluorinated Quaternary Stereogenic Centers

Zhao, Yujun ; Pan, Yuanhang ; Liu, Hongjun ; Yang, Yuanyong ; Jiang, Zhiyong ; Tan, Choon-Hong

Chemistry : a European journal, 2011-03, Vol.17 (13), p.3571-3574 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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9
Recent Advances in Organocatalytic Methods for Asymmetric CC Bond Formation
Recent Advances in Organocatalytic Methods for Asymmetric CC Bond Formation
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Recent Advances in Organocatalytic Methods for Asymmetric CC Bond Formation

Scheffler, Ulf ; Mahrwald, Rainer

Chemistry : a European journal, 2013-10, Vol.19 (43), p.14346-14396 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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10
Azolium/Hydroquinone Organo‐Radical Co‐Catalysis: Aerobic C−C‐Bond Cleavage in Ketones
Azolium/Hydroquinone Organo‐Radical Co‐Catalysis: Aerobic C−C‐Bond Cleavage in Ketones
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Azolium/Hydroquinone Organo‐Radical Co‐Catalysis: Aerobic C−C‐Bond Cleavage in Ketones

Nakatsuji, Yuya ; Kobayashi, Yusuke ; Masuda, Sakyo ; Takemoto, Yoshiji

Chemistry : a European journal, 2021-02, Vol.27 (8), p.2633-2637 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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