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1. Full Text Direct C(sp2)C(sp3) Cross‐Coupling of Diaryl Zinc Reagents with Benzylic, Primary, Secondary, and Tertiary Alkyl Halides
by Dunsford, Jay J and Clark, Ewan R and Ingleson, Michael J
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2015, Volume 54, Issue 19, pp. 5688 - 5692
The direct C(sp2)C(sp3) cross‐coupling of diaryl zinc reagents with benzylic, primary, secondary, and tertiary alkyl halides proceeded in the absence of... 
cross‐coupling | alkyl halides | organozinc reagents | zinc | synthetic methods | cross-coupling | ARYLATIONS | ANION | COMPLEXES | ELECTROPHILES | CHEMISTRY, MULTIDISCIPLINARY | Zinc | Solvents | Construction | Purification | Catalysts | Ambient temperature | Halides | Tolerances | Arrays
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2. Organozinc reagents
: a practical approach
by Jones, Philip, 1971 and Knochel, Paul
1999, Practical approach in chemistry series, ISBN 9780198501213, xiv, 354
Organozinc compounds
Book
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3. Full Text Palladium‐Catalyzed Formylation of Alkenylzinc Reagents with S‐(4‐Nitrophenyl) Thioformate
by Haraguchi, Ryosuke and Tanazawa, Sho‐go and Tokunaga, Naoya and Fukuzawa, Shin‐ichi
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2018, Volume 2018, Issue 15, pp. 1761 - 1764
We report the synthesis of enal compounds by palladium‐catalyzed formylation of alkenylzinc reagents with S‐(4‐nitrophenyl) thioformate. Various functional... 
Organozinc | Cross coupling | Palladium | Synthetic methods | Formylation | ALPHA,BETA-UNSATURATED ALDEHYDES | CHEMISTRY, ORGANIC | THIOL ESTERS | ZWITTERIONIC RHODIUM COMPLEX | ALKYNES | REGIOSELECTIVE HYDROFORMYLATION | TRIPHENYL PHOSPHITE | CARBON-MONOXIDE | ARYL HALIDES | ORGANIC HALIDES | TIN HYDRIDE | Chemical tests and reagents
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4. Organozinc reagents in organic synthesis
by Erdik, Ender
1996, New directions in organic and biological chemistry, ISBN 9780849391514, 411
Organozinc compounds | Synthesis | Organic compounds
Book
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5. Full Text Addition of Organozinc Reagents to Glycopyranosyl Cyanides: Access to Keto Ester‐C‐glycosides or Unsaturated Acyl‐C‐glycosides
by Ella Obame, Idriss and Ireddy, Prathap and Guisot, Nicolas E. S and Nourry, Arnaud and Saluzzo, Christine and Dujardin, Gilles and Dubreuil, Didier and Pipelier, Muriel and Guillarme, Stéphane
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2018, Volume 2018, Issue 14, pp. 1735 - 1738
Addition of Reformatsky‐type or allylic zinc reagents to 2,3,4,6‐tetra‐O‐benzylglycopyranosyl cyanides led to keto ester‐C‐glycosides or unsaturated... 
Carbohydrates | Organozinc reagents | Keto esters | C‐glycosides | Addition reactions | C-glycosides | GLYCOGEN-PHOSPHORYLASE INHIBITORS | ROUTE | ACID | ANALOG | D-GLUCOPYRANOSYL | CHEMISTRY, ORGANIC | Chemical tests and reagents | Cyanides | Organic chemistry | Chemical Sciences
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6. Full Text Cobalt‐Catalyzed Cross‐Coupling of 3‐ and 4‐Iodopiperidines with Grignard Reagents
by Gonnard, Laurine and Guérinot, Amandine and Cossy, Janine
Chemistry – A European Journal, ISSN 0947-6539, 09/2015, Volume 21, Issue 36, pp. 12797 - 12803
A cobalt‐catalyzed cross‐coupling between 3‐ and 4‐iodopiperidines and Grignard reagents is disclosed. The reaction is an efficient, cheap, chemoselective, and... 
piperidines | catalysis | cobalt | cross‐coupling | synthetic methods | cross-coupling | HETEROARYL BROMIDES | ROOM-TEMPERATURE | REDUCTIVE ALLYLATION | CHEMISTRY, MULTIDISCIPLINARY | ORGANOZINC REAGENTS | DOPAMINE-RECEPTOR | ARYLZINC REAGENTS | AMINO-ACIDS | 6-HALO-1-HEXENE DERIVATIVES | HECK REACTION | SECONDARY ALKYL-HALIDES | Chemical tests and reagents | Cobalt | Catalysis | Cross coupling | Synthesis | Joining | Formations | Piperidine | Scaffolds | Radicals
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7. Full Text Nickel‐Catalyzed Cross‐Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents
by Xie, Lan‐Gui and Wang, Zhong‐Xia
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2011, Volume 50, Issue 21, pp. 4901 - 4904
Broad scope and good tolerance: An efficient cross‐coupling of aryltrimethylammonium iodide salts with aryl‐, methyl‐, and benzylzinc chlorides catalyzed by... 
nickel | CN activation | homogeneous catalysis | cross‐coupling | organozinc reagents | cross-coupling | C-N activation | CARBON-NITROGEN | BOND FORMATION | CHEMISTRY, MULTIDISCIPLINARY | ALKYL-HALIDES | DIETHYL PHOSPHITE | ANILINE DERIVATIVES | SELECTIVE SYNTHESIS | EFFICIENT | ARYL CHLORIDES | GRIGNARD-REAGENTS | ALKENYLATION
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8. Full Text Cross‐Coupling of Aryl/Alkenyl Pivalates with Organozinc Reagents through Nickel‐Catalyzed CO Bond Activation under Mild Reaction Conditions
by Li, Bi‐Jie and Li, Yi‐Zhou and Lu, Xing‐Yu and Liu, Jia and Guan, Bing‐Tao and Shi, Zhang‐Jie
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2008, Volume 47, Issue 52, pp. 10124 - 10127
Finding the right partner: The catalyst system [NiCl2(PCy3)2] mediates the title transformation with high efficiency and allows aryl–aryl and vinyl–aryl... 
nickel | homogeneous catalysis | CO activation | cross‐coupling | organozinc reagents | Organozinc reagents | Nickel | Cross-coupling | Homogeneous catalysis | C-O activation | F BONDS | ARYL GRIGNARD-REAGENTS | EXCHANGE-REACTION | COMPLEXES | CARBON-CARBON BONDS | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | ETHERS | MESYLATES | cross-coupling | CHLORIDES | ORGANIC HALIDES | Nickel - chemistry | Oxygen - chemistry | Pentanoic Acids - chemistry | Organometallic Compounds - chemistry | Catalysis | Zinc - chemistry | Carbon - chemistry
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9. Full Text Advances in the chemistry of organozinc reagents
by Dilman, Alexander D and Levin, Vitalij V
Tetrahedron Letters, ISSN 0040-4039, 09/2016, Volume 57, Issue 36, pp. 3986 - 3992
Novel methods for the preparation and reactions of organozinc reagents are reviewed. In recent years, organozinc compounds have emerged as valuable reagents... 
Organozinc reagents | Negishi cross-coupling | Halogen/zinc exchange | Transmetalation | 3-COMPONENT SYNTHESIS | CARBOZINCATION | HIGHLY SELECTIVE METALATIONS | SECONDARY | CHEMISTRY, ORGANIC | ALKYL-HALIDES | 1,4-COBALT MIGRATION | MAGNESIUM | ZINC REAGENTS | ARYLZINC REAGENTS | COBALT-CATALYZED ADDITION | Chemical tests and reagents | Nitriles
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10. Full Text Nickel-Catalyzed Negishi Cross-Coupling of N-Acylsuccinimides: Stable, Amide-Based, Twist-Controlled Acyl-Transfer Reagents via N–C Activation
by Shi, Shicheng and Szostak, Michal
Synthesis, ISSN 0039-7881, 08/2017, Volume 49, Issue 16, pp. 3602 - 3608
Abstract This paper reports a room temperature, nickel-catalyzed Negishi cross-coupling of N -acylsuccinimides with arylzinc reagents via selective N–C bond... 
special topic | nickel | twisted amides | acyl transfer | amide cross-coupling | N-C activation | succinimide | Negishi cross-coupling | CHEMISTRY, ORGANIC | CHEMOSELECTIVE KETONE SYNTHESIS | DIARYL KETONE | BOND-CLEAVAGE | GENERAL-METHOD | ORGANOZINC REAGENTS | SECONDARY AMIDES | ESTERS | NITROGEN | ARYL | TRANSAMIDATION
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11. Full Text Late‐Stage Functionalization of Peptides and Cyclopeptides Using Organozinc Reagents
by Leroux, Marcel and Vorherr, Thomas and Lewis, Ian and Schaefer, Michael and Koch, Guido and Karaghiosoff, Konstantin and Knochel, Paul
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2019, Volume 58, Issue 24, pp. 8231 - 8234
We report a new late‐stage functionalization of small peptides and cyclopeptides relying on the Negishi cross‐coupling of readily prepared iodotyrosine‐ or... 
cross-coupling | peptides | organozinc | cyclopeptides | membrane permeability | HALIDES | DRUG | POSTSYNTHETIC MODIFICATION | BIOACTIVE PEPTIDES | ACIDIC HYDROGEN-ATOMS | ORGANOMETALLICS | CHEMISTRY, MULTIDISCIPLINARY | ZINC REAGENTS | CATALYZED CROSS-COUPLINGS | ORAL BIOAVAILABILITY | ARYL | Peptides | Permeability | Parameter modification | Halides | Aromatic compounds | Reagents | Membrane permeability
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12. Full Text Iron-catalyzed alkylation of alkenyl grignard reagents
by Cahiez, Gérard and Duplais, Christophe and Moyeux, Alban
Organic Letters, ISSN 1523-7060, 08/2007, Volume 9, Issue 17, pp. 3253 - 3254
The first iron-catalyzed cross-coupling reaction between alkenyl Grignard reagents and n- or s-alkyl bromides is described. The reaction is stereoselective and... 
CARBON BOND FORMATION | ORGANOZINC REAGENTS | HALIDES | ORGANIC-SYNTHESIS | CROSS-COUPLING REACTIONS | ORGANOMETALLIC REAGENTS | EFFICIENT SYNTHESIS | CHLORIDES | CHEMISTRY, ORGANIC | ARYL GRIGNARDS | BEARING BETA-HYDROGENS
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13. Full Text Nickel‐Catalyzed Cross‐Coupling of Arene‐ or Heteroarenecarbonitriles with Aryl‐ or Heteroarylmanganese Reagents through CCN Bond Activation
by Liu, Ning and Wang, Zhong‐Xia
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2012, Volume 354, Issue 9, pp. 1641 - 1645
The nickel‐catalyzed cross‐coupling reaction of arene‐ or heteroarenecarbonitriles with aryl‐ or heteroarylmanganese reagents via CCN bond activation has been... 
nickel | catalysis | nitriles | cross‐coupling | CCN bond activation | organomanganese reagents | cross-coupling | C-CN bond activation | CARBON-CYANO BONDS | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | C?CN bond activation | ALKYL-HALIDES | ORGANOZINC REAGENTS | DIETHYL PHOSPHITE | CHLORIDES | SELECTIVE SYNTHESIS | CHEMISTRY, APPLIED | GRIGNARD-REAGENTS | UNSYMMETRICAL BIARYLS | Synthesis | Nitriles | Activation | Nickel | Catalysis | Bonding | Functional groups
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14. Full Text MgCl2‐Accelerated Addition of Functionalized Organozinc Reagents to Aldehydes, Ketones, and Carbon Dioxide
by Metzger, Albrecht and Bernhardt, Sebastian and Manolikakes, Georg and Knochel, Paul
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2010, Volume 49, Issue 27, pp. 4665 - 4668
Pump it up! The sluggish reactivity of organozinc reagents in additions to aldehydes, ketones, and CO2 can be increased by MgCl2, which is usually generated in... 
carbon dioxide | carbonyl addition | ibuprofen | magnesium chloride | organozinc reagents | Organozinc reagents | Magnesium chloride | Carbonyl addition | Carbon dioxide | Ibuprofen | HALIDES | ASYMMETRIC-SYNTHESIS | MECHANISM | ARYLZINC COMPOUNDS | ALKYLATION | COMPLEXES | DIRECT INSERTION | REACTIVITY | CHEMISTRY, MULTIDISCIPLINARY | ZINC REAGENTS | CATALYSTS
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15. Full Text Efficient C(sp3)–H Bond Arylation of Tetrahydroisoquinolines with Knochel-Type Arylzinc Reagents under Oxidative Conditions
by Peng, Zhihua and Yu, Zhi and Chen, Dong-Huang and Liang, Shuyuan and Zhang, Liwei and Zhao, Dezhi and Song, Linhua and Jiang, Cuiyu
Synlett, ISSN 0936-5214, 09/2017, Volume 28, Issue 14, pp. 1835 - 1839
Abstract A novel C(sp 3 )–H bond arylation of tetrahydroisoquinoline (THIQ) derivatives with Knochel-type arylzinc reagents has been developed. In the presence... 
letter | tetrahydroisoquinolines | esters | arylzinc reagents | arylation | oxidative conditions | ACTIVATION | ALKYLATION | IMINES | AMIDATION | CHEMISTRY, ORGANIC | C-H BONDS | ORGANOZINC REAGENTS | BORONIC ACIDS | FUNCTIONALIZATION | MILD CONDITIONS | CATALYZED DIRECT ARYLATION
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16. Full Text Palladium‐Catalyzed Cross‐Coupling of Unactivated Aryl Sulfides with Arylzinc Reagents under Mild Conditions
by Otsuka, Shinya and Fujino, Daishi and Murakami, Kei and Yorimitsu, Hideki and Osuka, Atsuhiro
Chemistry – A European Journal, ISSN 0947-6539, 10/2014, Volume 20, Issue 41, pp. 13146 - 13149
Cross‐coupling of general aryl alkyl sulfides with arylzinc reagents proceeds smoothly, even at room temperature or below, with a palladium–N‐heterocyclic... 
palladium | organozinc compounds | cross‐coupling | CS bond activation | organosulfur compounds | C-S bond activation | Palladium | Cross-coupling | Organozinc compounds | Organosulfur compounds | cross-coupling | ORGANIC-SYNTHESIS | BOND-FORMING REACTIONS | THIOL ESTERS | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | HETEROAROMATIC THIOETHER | BORONIC ACIDS | PUMMERER REACTION | organozic compounds | C-S ACTIVATION | CARBON-CARBON | GRIGNARD-REAGENTS | Palladium catalysts | Sulfides | Chemical tests and reagents | Cross coupling | Catalysts | Aromatic compounds | Chemical reactions | Transformations | Carbenes
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