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1
Hydrogenation of Propene on Cobalt Fischer–Tropsch Catalysts
Hydrogenation of Propene on Cobalt Fischer–Tropsch Catalysts
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Hydrogenation of Propene on Cobalt Fischer–Tropsch Catalysts

Aaserud, Christian ; Hilmen, Anne-Mette ; Bergene, Edvard ; Eric, Sigrid ; Schanke, Dag ; Holmen, Anders

Catalysis letters, 2004-05, Vol.94 (3), p.171-176 [Peer Reviewed Journal]

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2
1,2-Addition of α,α,α-Trichlorotoluene to Ketones via a Mg Barbier Reaction in DMF: New Route to Cycloalk-1-en-1-yl and Alk-1-en-1-yl Phenyl Ketones
1,2-Addition of α,α,α-Trichlorotoluene to Ketones via a Mg Barbier Reaction in DMF: New Route to Cycloalk-1-en-1-yl and Alk-1-en-1-yl Phenyl Ketones
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1,2-Addition of α,α,α-Trichlorotoluene to Ketones via a Mg Barbier Reaction in DMF: New Route to Cycloalk-1-en-1-yl and Alk-1-en-1-yl Phenyl Ketones

Aaziz, Akima ; Oudeyer, Sylvain ; Léonel, Eric ; Paugam, Jean Paul ; Nédélec, Jean-Yves

Synthetic communications, 2007-04-01, Vol.37 (7), p.1147-1154 [Peer Reviewed Journal]

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3
Dopamine/Serotonin Receptor Ligands, Part III [1]: Synthesis and Biological Activities of 7, 7′—Alkylene‐bis‐6, 7, 8, 9, 14, 15‐hexahydro‐5H‐benz[d]indolo[2, 3‐g]azecines — Application of the Bivalent Ligand Approach to a Novel Type of Dopamine Receptor Antagonist
Dopamine/Serotonin Receptor Ligands, Part III [1]: Synthesis and Biological Activities of 7, 7′—Alkylene‐bis‐6, 7, 8, 9, 14, 15‐hexahydro‐5H‐benz[d]indolo[2, 3‐g]azecines — Application of the Bivalent Ligand Approach to a Novel Type of Dopamine Receptor Antagonist
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Dopamine/Serotonin Receptor Ligands, Part III [1]: Synthesis and Biological Activities of 7, 7′—Alkylene‐bis‐6, 7, 8, 9, 14, 15‐hexahydro‐5H‐benz[d]indolo[2, 3‐g]azecines — Application of the Bivalent Ligand Approach to a Novel Type of Dopamine Receptor Antagonist

Abadi, Ashraf H ; Lankow, Stefan ; Hoefgen, Barbara ; Decker, Michael ; Kassack, Matthias U ; Lehmann, Jochen

Archiv der Pharmazie (Weinheim), 2002-11, Vol.335 (8), p.367-373

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4
Asymmetric Intramolecular Hydroamination of Alkenes in Mild and Wet Conditions—Structure and Reactivity of Cationic Binuclear Gold(I) Catalysts
Asymmetric Intramolecular Hydroamination of Alkenes in Mild and Wet Conditions—Structure and Reactivity of Cationic Binuclear Gold(I) Catalysts
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Asymmetric Intramolecular Hydroamination of Alkenes in Mild and Wet Conditions—Structure and Reactivity of Cationic Binuclear Gold(I) Catalysts

Abadie, Marc‐Antoine ; Trivelli, Xavier ; Medina, Florian ; Capet, Frédéric ; Roussel, Pascal ; Agbossou‐Niedercorn, Francine ; Michon, Christophe

ChemCatChem, 2014-08, Vol.6 (8), p.2235-2239 [Peer Reviewed Journal]

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5
Gold(I)‐Catalysed Asymmetric Hydroamination of Alkenes: A Silver‐ and Solvent‐Dependent Enantiodivergent Reaction
Gold(I)‐Catalysed Asymmetric Hydroamination of Alkenes: A Silver‐ and Solvent‐Dependent Enantiodivergent Reaction
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Gold(I)‐Catalysed Asymmetric Hydroamination of Alkenes: A Silver‐ and Solvent‐Dependent Enantiodivergent Reaction

Abadie, Marc‐Antoine ; Trivelli, Xavier ; Medina, Florian ; Duhal, Nathalie ; Kouach, Mostafa ; Linden, Bernhard ; Génin, Eric ; Vandewalle, Maxence ; Capet, Frédéric ; Roussel, Pascal ; Del Rosal, Iker ; Maron, Laurent ; Agbossou‐Niedercorn, Francine ; Michon, Christophe

Chemistry : a European journal, 2017-08-10, Vol.23 (45), p.10777-10788

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Frontispiece: Gold(I)‐Catalysed Asymmetric Hydroamination of Alkenes: A Silver‐ and Solvent‐Dependent Enantiodivergent Reaction
Frontispiece: Gold(I)‐Catalysed Asymmetric Hydroamination of Alkenes: A Silver‐ and Solvent‐Dependent Enantiodivergent Reaction
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Frontispiece: Gold(I)‐Catalysed Asymmetric Hydroamination of Alkenes: A Silver‐ and Solvent‐Dependent Enantiodivergent Reaction

Abadie, Marc‐Antoine ; Trivelli, Xavier ; Medina, Florian ; Duhal, Nathalie ; Kouach, Mostafa ; Linden, Bernhard ; Génin, Eric ; Vandewalle, Maxence ; Capet, Frédéric ; Roussel, Pascal ; Del Rosal, Iker ; Maron, Laurent ; Agbossou‐Niedercorn, Francine ; Michon, Christophe

Chemistry : a European journal, 2017-08-10, Vol.23 (45), p.n/a

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7
(Salen)Mn-Catalyzed Epoxidation of Alkenes:  A Two-Zone Process with Different Spin-State Channels as Suggested by DFT Study
(Salen)Mn-Catalyzed Epoxidation of Alkenes:  A Two-Zone Process with Different Spin-State Channels as Suggested by DFT Study
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(Salen)Mn-Catalyzed Epoxidation of Alkenes:  A Two-Zone Process with Different Spin-State Channels as Suggested by DFT Study

Abashkin, Yuri G ; Burt, Stanley K

Organic letters, 2004-01-08, Vol.6 (1), p.59-62 [Peer Reviewed Journal]

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8
A new class of organoplatinum-based DFNS for the production of cyclic carbonates from olefins and CO2
A new class of organoplatinum-based DFNS for the production of cyclic carbonates from olefins and CO2
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A new class of organoplatinum-based DFNS for the production of cyclic carbonates from olefins and CO2

Abassian, Maryam ; Zhiani, Rahele ; Motavalizadehkakhky, Alireza ; Eshghi, Hossein ; Mehrzad, Jamshid

RSC advances, 2020-04-16, Vol.1 (26), p.1544-1551 [Peer Reviewed Journal]

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9
Mn(III)‐salan/graphene oxide/magnetite nanocomposite as a highly selective catalyst for aerobic epoxidation of olefins
Mn(III)‐salan/graphene oxide/magnetite nanocomposite as a highly selective catalyst for aerobic epoxidation of olefins
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Mn(III)‐salan/graphene oxide/magnetite nanocomposite as a highly selective catalyst for aerobic epoxidation of olefins

Abbasi, Vahideh ; Hosseini‐Monfared, Hassan ; Hosseini, Seyed Majid

Applied organometallic chemistry, 2017-02, Vol.31 (2), p.n/a [Peer Reviewed Journal]

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10
Influence of various aluminum distributions on modification of ZSM-5 zeolite framework with cobalt ions in alkane catalytic cracking
Influence of various aluminum distributions on modification of ZSM-5 zeolite framework with cobalt ions in alkane catalytic cracking
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Influence of various aluminum distributions on modification of ZSM-5 zeolite framework with cobalt ions in alkane catalytic cracking

Abbasizadeh, Saeed ; Abbasizadeh, Saeed ; Karimzadeh, Ramin ; Karimzadeh, Ramin Wook Bae, Jong ; Tomishige, Keiichi ; Yang, Jung-Il ; Wook Bae, Jong ; Tomishige, Keiichi ; Yang, Jung-Il

Research on chemical intermediates, 2019-03-15, Vol.45 (3), p.955-972 [Peer Reviewed Journal]

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