Nickel-catalysed carbonylative homologation of aryl iodides

[1]  Fu‐Peng Wu,et al.  First-Row Transition-Metal-Catalyzed Carbonylative Transformations of Carbon Electrophiles. , 2019, Chemical reviews.

[2]  M. Larhed,et al.  Palladium-Catalyzed Molybdenum Hexacarbonyl-Mediated Gas-Free Carbonylative Reactions , 2018, Synlett.

[3]  Fu‐Peng Wu,et al.  Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides , 2018, iScience.

[4]  Fu‐Peng Wu,et al.  Nickel-Catalyzed Molybdenum-Promoted Carbonylative Synthesis of Benzophenones. , 2018, The Journal of organic chemistry.

[5]  Z. Gu,et al.  Enantioselective Synthesis of Biaryl Atropisomers via Pd/Norbornene-Catalyzed Three-Component Cross-Couplings , 2018 .

[6]  Fu‐Peng Wu,et al.  Direct synthesis of benzylic amines by palladium-catalyzed carbonylative aminohomologation of aryl halides , 2018, Communications Chemistry.

[7]  P. Kalck,et al.  Tandem Hydroaminomethylation Reaction to Synthesize Amines from Alkenes. , 2018, Chemical reviews.

[8]  Xiao‐Feng Wu,et al.  Ligand- and Solvent-Controlled Regio- and Chemodivergent Carbonylative Reactions. , 2018, Angewandte Chemie.

[9]  T. Skrydstrup,et al.  Carbonylative Coupling of Alkyl Zinc Reagents with Benzyl Bromides Catalyzed by a Nickel/NN2  Pincer Ligand Complex. , 2018, Angewandte Chemie.

[10]  Fu‐Peng Wu,et al.  Palladium‐Catalyzed Carbonylative Homocoupling of Aryl Iodides for the Synthesis of Symmetrical Diaryl Ketones with Formic Acid , 2018 .

[11]  Fu‐Peng Wu,et al.  Palladium-catalyzed carbonylative Sonogashira coupling of aryl diazonium salts with formic acid as the CO source: the effect of 1,3-butadiene , 2017 .

[12]  Fu‐Peng Wu,et al.  Direct Palladium-Catalyzed Carbonylative Transformation of Allylic Alcohols and Related Derivatives. , 2017, Organic letters.

[13]  Fu‐Peng Wu,et al.  Palladium-Catalyzed Carbonylative Transformation of Organic Halides with Formic Acid as the Coupling Partner and CO Source: Synthesis of Carboxylic Acids. , 2017, The Journal of organic chemistry.

[14]  Fu‐Peng Wu,et al.  Palladium‐Catalyzed Ligand‐Controlled Selective Synthesis of Aldehydes and Acids from Aryl Halides and Formic Acid , 2017 .

[15]  Hui Yu,et al.  Charge-Transfer Complex Promoted C-N Bond Activation for Ni-Catalyzed Carbonylation. , 2017, Organic letters.

[16]  Linhua Song,et al.  Efficient C(sp3)–H Bond Arylation of Tetrahydroisoquinolines with Knochel-Type Arylzinc Reagents under Oxidative Conditions , 2017 .

[17]  Fu‐Peng Wu,et al.  A Convenient and Efficient Palladium‐Catalyzed Carbonylative Sonogashira Transformation with Formic Acid as the CO Source , 2017 .

[18]  YueXia Bai,et al.  Natural Product Synthesis via Palladium-Catalyzed Carbonylation. , 2017, The Journal of organic chemistry.

[19]  Xiao‐Feng Wu,et al.  Recent Achievements in Carbonylation Reactions: A Personal Account , 2016, Synlett.

[20]  Z. Gu,et al.  The palladium/norbornene-catalyzed ortho-silylmethylation reaction: a practical protocol for ortho-functionalized one-carbon homologation of aryl iodides. , 2016, Chemical communications.

[21]  Xiao‐Feng Wu,et al.  Visible Light-Induced Carbonylation Reactions with Organic Dyes as the Photosensitizers. , 2016, ChemSusChem.

[22]  Xiao‐Feng Wu.  Palladium-catalyzed carbonylative transformation of aryl chlorides and aryl tosylates , 2016 .

[23]  B. Gabriele,et al.  Oxidative Carbonylation as a Powerful Tool for the Direct Synthesis of Carbonylated Heterocycles , 2012 .

[24]  M. Larhed,et al.  Molybdenum Hexacarbonyl Mediated CO Gas-Free Carbonylative Reactions , 2012 .

[25]  M. Larhed,et al.  Molybdenum Hexacarbonyl MediatedCO Gas-Free Carbonylative Reactions , 2012 .

[26]  H. Neumann,et al.  Palladium-catalyzed carbonylative coupling reactions between Ar-X and carbon nucleophiles. , 2011, Chemical Society reviews.

[27]  M. Hamann,et al.  Marine indole alkaloids: potential new drug leads for the control of depression and anxiety. , 2010, Chemical reviews.

[28]  T. Kawasaki,et al.  Simple indole alkaloids and those with a nonrearranged monoterpenoid unit. , 2005, Natural product reports.

[29]  S. O’Connor,et al.  Chemistry and biology of monoterpene indole alkaloid biosynthesis. , 2006, Natural product reports.

[30]  T. Ziegler.  Synthesis from Carboxylic Acids , 2005 .

[31]  H. Bestmann,et al.  Further Improvements of the Synthesis of Alkynes from Aldehydes , 2003 .

[32]  A. Katritzky,et al.  One-carbon homologation of carboxylic acids via BtCH(2)TMS: a safe alternative to the Arndt--Eistert reaction. , 2001, The Journal of organic chemistry.

[33]  Fang,et al.  BtCH(2)TMS-assisted homologation of carboxylic acids: A safe alternative to the arndt-eistert reaction , 2000, Organic letters.

[34]  M. Haque,et al.  Ester homologation via .alpha.-bromo .alpha.-keto dianion rearrangement , 1985 .

[35]  Rex Taylor.  Personal Account , 1979 .

[36]  L. Cassar,et al.  Nickel-catalyzed carbonylation of aromatic halides at atmospheric pressure of carbon monoxide , 1973 .

[37]  R. T. Arnold,et al.  The Mechanism of the Arndt-Eistert Reaction1 , 1942 .