| scholarly article | Q13442814 |
| P2093 | author name string | Gregory C Fu | |
| Nathan A Owston | |||
| Francesco Tramutola | |||
| Ashraf Wilsily | |||
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| Transmetalation of Alkylboranes to Palladium in the Suzuki Coupling Reaction Proceeds with Retention of Stereochemistry | Q34098839 | ||
| Alkylboranes in the Suzuki-Miyaura Coupling: Stereochemical and Mechanistic Studies | Q34098845 | ||
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| P433 | issue | 13 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 5794-5797 | |
| P577 | publication date | 2012-03-26 | |
| P1433 | published in | Journal of the American Chemical Society | Q898902 |
| P1476 | title | New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles | |
| P478 | volume | 134 |
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| Q50962098 | Highly Efficient, Convergent, and Enantioselective Synthesis of Phthioceranic Acid. |
| Q89703145 | Highly stereoselective nickel-catalyzed difluoroalkylation of aryl ketones to tetrasubstituted monofluoroalkenes and quaternary alkyl difluorides |
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| Q37701679 | Ligand-controlled asymmetric arylation of aliphatic α-amino anion equivalents. |
| Q46705158 | Mechanism and Origins of Ligand-Controlled Stereoselectivity of Ni-Catalyzed Suzuki-Miyaura Coupling with Benzylic Esters: A Computational Study |
| Q46441169 | Mechanistic Study of an Improved Ni Precatalyst for Suzuki-Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species |
| Q38942612 | Ni-Catalyzed C-C Couplings Using Alkyl Electrophiles |
| Q48341819 | Ni-Catalyzed Enantioselective Conjunctive Coupling with C(sp3) Electrophiles: A Radical-Ionic Mechanistic Dichotomy. |
| Q60311327 | Nickel-Catalyzed 1,2-Diarylation of Simple Alkenyl Amides |
| Q41828474 | Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids. |
| Q48348457 | Nickel-Catalyzed Enantioselective Conjunctive Cross-Coupling of 9-BBN Borates |
| Q48366284 | Nickel-Catalyzed Heck-Type Monofluoroacetation of Styrenes for Facile Synthesis of Allylic Fluorides |
| Q36539814 | Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations |
| Q36063009 | Nickel-catalyzed coupling reactions of alkyl electrophiles, including unactivated tertiary halides, to generate carbon-boron bonds. |
| Q36078422 | Nickel-catalyzed cross-coupling of photoredox-generated radicals: uncovering a general manifold for stereoconvergence in nickel-catalyzed cross-couplings |
| Q37405693 | Nickel/bis(oxazoline)-catalyzed asymmetric Negishi arylations of racemic secondary benzylic electrophiles to generate enantioenriched 1,1-diarylalkanes |
| Q92935904 | Palladium-Catalyzed Intramolecular Oxidative Arylations for the Synthesis of Fused Biaryl Sulfones |
| Q50455391 | Palladium-catalyzed intramolecular reductive cross-coupling of Csp2-Csp3 bond formation |
| Q28082232 | Recent developments in the Suzuki-Miyaura reaction: 2010-2014 |
| Q55228213 | Reductive coupling of benzyl oxalates with highly functionalized alkyl bromides by nickel catalysis. |
| Q42169462 | Retention or inversion in stereospecific nickel-catalyzed cross-coupling of benzylic carbamates with arylboronic esters: control of absolute stereochemistry with an achiral catalyst |
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| Q41762404 | Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters |
| Q39135537 | Synthesis and reactivity of new aminophenolate complexes of nickel |
| Q90215411 | Synthesis of chiral diamine ligands for nickel-catalyzed asymmetric cross-couplings of alkylchloroboronate esters with alkylzincs: (1R,2R)-N,N'-dimethyl-1,2-bis(2-methylphenyl)-1,2-diaminoethane |
| Q52782591 | Synthesis of chiral heterocycles by ligand-controlled regiodivergent and enantiospecific Suzuki Miyaura cross-coupling. |
| Q46933137 | Synthesis of chiral α-hydroxy acids via palladium-catalyzed C(sp(3))-H alkylation of lactic acid |
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| Q41162504 | Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes |
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