Formates plus triazabicyclodecene (TBD): an efficient platform for non-gaseous carbonylation and unexpected hydrogenation
暂无分享,去创建一个
[1] Diksha Singh,et al. Ruthenium-Catalyzed C-H Functionalization of Benzoic Acids with Allyl Alcohols: A Controlled Reactivity Switch between C-H Alkenylation and C-H Alkylation Pathways. , 2018, Organic letters.
[2] Junliang Zhang,et al. Palladium-Catalyzed Enantioselective Reductive Heck Reactions: Convenient Access to 3,3-Disubstituted 2,3-Dihydrobenzofuran. , 2018, Angewandte Chemie.
[3] M. Krische,et al. Enantioselective Iridium-Catalyzed Phthalide Formation through Internal Redox Allylation of Phthalaldehydes. , 2018, Angewandte Chemie.
[4] Y. Ishikawa,et al. Mechanistic Insight into Weak-Base-Catalyzed Generation of Carbon Monoxide from Phenyl Formate and Its Application to Catalytic Carbonylation at Room Temperature without Use of External Carbon Monoxide Gas , 2017 .
[5] Hongwei Zhou,et al. CuX-Activated N-Halosuccinimide: Synthesis of 3-Haloquinolines via Electrophilic Cyclization of Alkynyl Imines. , 2017, The Journal of organic chemistry.
[6] Jieping Zhu,et al. Water as a Hydride Source in Palladium-Catalyzed Enantioselective Reductive Heck Reactions. , 2017, Angewandte Chemie.
[7] Xiao‐Feng Wu,et al. Iridium-Catalyzed Carbonylative Synthesis of Chromenones from Simple Phenols and Internal Alkynes at Atmospheric Pressure. , 2016, Angewandte Chemie.
[8] Hanmin Huang,et al. Palladium-Catalyzed Intramolecular Hydroaminocarbonylation to Lactams: Additive-Free Protocol Initiated by Palladium Hydride , 2016 .
[9] Hongwei Zhou,et al. Acetyl Bromide Promoted Sequence via Allene Intermediates: Metal‐Free Construction of 2,3‐Dihydroindenes and Isoindolines , 2016 .
[10] Jean-Claude Berthet,et al. Implications of CO2 Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+ Frustrated Lewis Pairs , 2016 .
[11] T. Skrydstrup,et al. The Development and Application of Two-Chamber Reactors and Carbon Monoxide Precursors for Safe Carbonylation Reactions. , 2016, Accounts of chemical research.
[12] Hongwei Zhou,et al. Sulfone promoted Rh(III)-catalyzed C–H activation and base assisted 1,5-H shift strategy for the construction of seven-membered rings , 2015 .
[13] Kami L. Hull,et al. Chloroform as a Carbon Monoxide Precursor: In or Ex Situ Generation of CO for Pd-Catalyzed Aminocarbonylations. , 2015, Organic letters.
[14] Hongwei Zhou,et al. Selectfluor-Promoted Sequential Reactions via Allene Intermediates: Metal-Free Construction of Fused Polycyclic Skeletons. , 2015, The Journal of organic chemistry.
[15] Hongwei Zhou,et al. From Acyliminiums/Amidoallenyliums to Highly Functionalized Allene Intermediates: Stereoselective Preparation of Z‐Amidovinyl‐Furans, ‐Pyrroles, ‐Thiophenes, ‐Benzofurans and ‐Benzothiophenes , 2015 .
[16] M. Beller,et al. Selective palladium-catalyzed aminocarbonylation of 1,3-dienes: atom-efficient synthesis of β,γ-unsaturated amides. , 2014, Journal of the American Chemical Society.
[17] H. Alper,et al. Pd-catalyzed chemoselective carbonylation of aminophenols with iodoarenes: alkoxycarbonylation vs aminocarbonylation. , 2014, Journal of the American Chemical Society.
[18] S. Buchwald,et al. Mild Pd-Catalyzed Aminocarbonylation of (Hetero)Aryl Bromides with a Palladacycle Precatalyst , 2014, Organic letters.
[19] K. Manabe,et al. Formic Acid Derivatives as Practical Carbon Monoxide Surrogates for Metal-Catalyzed Carbonylation Reactions , 2014 .
[20] I. S. Makarov,et al. Efficient fluoride-catalyzed conversion of CO2 to CO at room temperature. , 2014, Journal of the American Chemical Society.
[21] H. Neumann,et al. Aryl formate as bifunctional reagent: applications in palladium-catalyzed carbonylative coupling reactions using in situ generated CO. , 2014, Angewandte Chemie.
[22] B. Bhanage,et al. Recent developments in palladium catalysed carbonylation reactions , 2014 .
[23] Yian Shi,et al. A palladium-catalyzed regioselective hydroesterification of alkenylphenols to lactones with phenyl formate as CO source. , 2014, Organic letters.
[24] M. Beller,et al. Selective palladium-catalyzed aminocarbonylation of olefins with aromatic amines and nitroarenes. , 2013, Angewandte Chemie.
[25] K. Manabe,et al. Palladium-catalyzed fluorocarbonylation using N-formylsaccharin as CO source: general access to carboxylic acid derivatives. , 2013, Organic letters.
[26] K. Manabe,et al. Palladium-catalyzed reductive carbonylation of aryl halides with N-formylsaccharin as a CO source. , 2013, Angewandte Chemie.
[27] T. Fukuyama,et al. Modernized low pressure carbonylation methods in batch and flow employing common acids as a CO source. , 2013, Organic letters.
[28] H. Neumann,et al. Synthesis of heterocycles via palladium-catalyzed carbonylations. , 2013, Chemical reviews.
[29] Hongwei Zhou,et al. Synthesis of polyfunctionalized quinolines via the sequence of propargyl-allenyl isomerization and aza-electrocyclization. , 2012, The Journal of organic chemistry.
[30] J. Terao,et al. Palladium-catalyzed esterification of aryl halides using aryl formates without the use of external carbon monoxide. , 2012, Chemical communications.
[31] K. Manabe,et al. Palladium-catalyzed carbonylation of aryl, alkenyl, and allyl halides with phenyl formate. , 2012, Organic letters.
[32] T. Skrydstrup,et al. Palladium catalyzed carbonylative Heck reaction affording monoprotected 1,3-ketoaldehydes. , 2012, Organic letters.
[33] M. Larhed,et al. Molybdenum Hexacarbonyl MediatedCO Gas-Free Carbonylative Reactions , 2012 .
[34] T. Skrydstrup,et al. Silacarboxylic acids as efficient carbon monoxide releasing molecules: synthesis and application in palladium-catalyzed carbonylation reactions. , 2011, Journal of the American Chemical Society.
[35] B. Bhanage,et al. Palladium-catalyzed carbon-monoxide-free aminocarbonylation of aryl halides using N-substituted formamides as an amide source. , 2011, The Journal of organic chemistry.
[36] T. Skrydstrup,et al. Carbonylative Heck reactions using CO generated ex situ in a two-chamber system. , 2011, Organic letters.
[37] T. Skrydstrup,et al. Ex situ generation of stoichiometric and substoichiometric 12CO and 13CO and its efficient incorporation in palladium catalyzed aminocarbonylations. , 2011, Journal of the American Chemical Society.
[38] J. Terao,et al. Palladium‐Catalyzed Hydroesterification of Alkynes Employing Aryl Formates without the Use of External Carbon Monoxide , 2011 .
[39] M. Larhed,et al. Microwave-assisted synthesis of Weinreb and MAP aryl amides via Pd-catalyzed Heck aminocarbonylation using Mo(CO)6 or W(CO)6. , 2011, The Journal of organic chemistry.
[40] I. Omae. Transition metal-catalyzed cyclocarbonylation in organic synthesis , 2011 .
[41] J. Overgaard,et al. In situ generated bulky palladium hydride complexes as catalysts for the efficient isomerization of olefins. Selective transformation of terminal alkenes to 2-alkenes. , 2010, Journal of the American Chemical Society.
[42] Andreas Martin,et al. Catalytic reaction of methyl formate with amines to formamides , 2009 .
[43] W. Ren,et al. Palladium-catalyzed carbamoylation of aryl halides by tungsten carbonyl amine complex. , 2009, The Journal of organic chemistry.
[44] H. Neumann,et al. Palladium-catalyzed carbonylation reactions of aryl halides and related compounds. , 2009, Angewandte Chemie.
[45] S. Stahl,et al. Insertion of molecular oxygen into a palladium-hydride bond: computational evidence for two nearly isoenergetic pathways. , 2007, Journal of the American Chemical Society.
[46] H. Alper,et al. Palladium-catalyzed regiospecific aminocarbonylation of alkynes in the ionic liquid [bmim][Tf2N]. , 2006, Organic letters.
[47] Sukbok Chang,et al. Halide ions as a highly efficient promoter in the Ru-catalyzed hydroesterification of alkenes and alkynes. , 2006, Organic letters.
[48] K. Rossen,et al. A general and efficient method for the formylation of aryl and heteroaryl bromides. , 2005, Angewandte Chemie.
[49] K. Kakiuchi,et al. Evolution of carbonylation catalysis: no need for carbon monoxide. , 2004, Angewandte Chemie.
[50] P. Floreancig,et al. Investigations of the scope and mechanism of the tandem hydroesterification/lactonization reaction. , 2004, Organic letters.
[51] G. C. Fu,et al. Elucidating reactivity differences in palladium-catalyzed coupling processes: the chemistry of palladium hydrides. , 2004, Journal of the American Chemical Society.
[52] Sukbok Chang,et al. A novel chelation-assisted hydroesterification of alkenes via ruthenium catalysis. , 2002, Journal of the American Chemical Society.