Palladium‐Catalyzed Carbonylation in the Synthesis of N ‐Ynonylsulfoximines
暂无分享,去创建一个
C. Bolm | Ding Ma | Deshen Kong | Chenyang Wang | Peng Shi | Yongliang Tu
[1] Jian Zhang,et al. Application of sulfoximines in medicinal chemistry from 2013 to 2020. , 2020, European journal of medicinal chemistry.
[2] L. Kattner,et al. Sulfoximines as Rising Stars in Modern Drug Discovery? Current Status and Perspective on an Emerging Functional Group in Medicinal Chemistry. , 2020, Journal of medicinal chemistry.
[3] S. Das,et al. N−H and C−H Functionalization of Sulfoximine: Recent Advancement and Prospects , 2020 .
[4] T. Skrydstrup,et al. Controlled Release of Reactive Gases: A Tale of Taming Carbon Monoxide. , 2020, ChemPlusChem.
[5] Xiao‐Feng Wu,et al. Carbonylative synthesis of heterocycles involving diverse CO surrogates. , 2020, Chemical communications.
[6] Kaikai Wang,et al. Ynones in Reflex-Michael Addition, CuAAC, and Cycloaddition, as Well as their Use as Nucleophilic Enols, Electrophilic Ketones, and Allenic Precursors , 2020 .
[7] C. Bolm,et al. Chiral Analogues of PFI-1 as BET Inhibitors and Their Functional Role in Myeloid Malignancies. , 2020, ACS medicinal chemistry letters.
[8] C. Bolm,et al. Mechanochemical Palladium‐Catalyzed Carbonylative Reactions Using Mo(CO)6 , 2019, Chemistry.
[9] J. Yu,et al. Tandem Reactions of Ynones:viaConjugate Addition of Nitrogen‐, Carbon‐, Oxygen‐, Boron‐, Silicon‐, Phosphorus‐, and Sulfur‐Containing Nucleophiles , 2019, Advanced Synthesis & Catalysis.
[10] C. Bolm,et al. BN‐ and BO‐Doped Inorganic–Organic Hybrid Polymers with Sulfoximine Core Units , 2019, Chemistry.
[11] M. Yus,et al. Conjugated Ynones in Organic Synthesis. , 2019, Chemical reviews.
[12] B. Trost,et al. Sulfones as Chemical Chameleons: Versatile Synthetic Equivalents of Small Molecule Synthons. , 2019, Chemistry.
[13] K. Rissanen,et al. From One-Pot NH-Sulfoximidations of Thiophene Derivatives to Dithienylethene-Type Photoswitches. , 2019, Organic letters.
[14] U. Lücking. Neglected sulfur(vi) pharmacophores in drug discovery: exploration of novel chemical space by the interplay of drug design and method development , 2019, Organic Chemistry Frontiers.
[15] Xiao‐Feng Wu,et al. The Chemistry of CO: Carbonylation , 2019, Chem.
[16] Christopher A. Hone,et al. Continuous‐Flow Pd‐Catalyzed Carbonylation of Aryl Chlorides with Carbon Monoxide at Elevated Temperature and Pressure , 2019, ChemCatChem.
[17] C. Bolm,et al. Synthesis of N-Propargylsulfoximines by Copper-Catalyzed A3 -Couplings. , 2017, Chemistry.
[18] L. Degennaro,et al. Straightforward Strategies for the Preparation of NH-Sulfoximines: A Serendipitous Story , 2017, Synlett.
[19] Yan‐qin Yuan,et al. Palladium catalyzed aroylation of NH-sulfoximines with aryl halides using chloroform as the CO precursor , 2017 .
[20] M. Babazadeh,et al. Intramolecular cyclization of N-allyl propiolamides: a facile synthetic route to highly substituted γ-lactams (a review) , 2017 .
[21] Linhua Song,et al. Efficient C(sp3)–H Bond Arylation of Tetrahydroisoquinolines with Knochel-Type Arylzinc Reagents under Oxidative Conditions , 2017 .
[22] Xiao‐Feng Wu,et al. Palladium-Catalyzed Carbonylative Multicomponent Reactions. , 2017, Chemistry.
[23] D. Harki,et al. Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions. , 2017, Journal of medicinal chemistry.
[24] C. Bolm,et al. Sulfoximines from a Medicinal Chemist's Perspective: Physicochemical and in vitro Parameters Relevant for Drug Discovery. , 2017, European journal of medicinal chemistry.
[25] G. Sekar,et al. Sulfoximinocarbonylation of aryl halides using heterogeneous Pd/C catalyst , 2016 .
[26] Joyram Guin,et al. Direct N-Acylation of Sulfoximines with Aldehydes by N-Heterocyclic Carbene Catalysis under Oxidative Conditions , 2016 .
[27] Yusheng Wu,et al. Pd-catalyzed aminocarbonylation of alkynes with amines using Co2(CO)8 as a carbonyl source , 2016 .
[28] 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.
[29] Ian R. Baxendale,et al. The Use of Gases in Flow Synthesis , 2016 .
[30] Guangbin Dong,et al. Synthesis of Ynones and Recent Application in Transition-Metal-Catalyzed Reactions , 2015 .
[31] B. Bhanage,et al. Recent advances in the transition metal catalyzed carbonylation of alkynes, arenes and aryl halides using CO surrogates , 2015 .
[32] G. Roth,et al. Development of a Scalable Process for the Crop Protection Agent Isoclast , 2015 .
[33] Lin Zhu,et al. Synthesis of α-Methylene-β-Lactams via PPh3-Catalyzed Umpolung Cyclization of Propiolamides. , 2015, The Journal of organic chemistry.
[34] P. Arvidsson,et al. Synthesis of novel aryl and heteroaryl acyl sulfonimidamides via Pd-catalyzed carbonylation using a nongaseous precursor. , 2013, Organic letters.
[35] H. Neumann,et al. Synthesis of heterocycles via palladium-catalyzed carbonylations. , 2013, Chemical reviews.
[36] M. Larhed,et al. Molybdenum Hexacarbonyl MediatedCO Gas-Free Carbonylative Reactions , 2012 .
[37] Aiwen Lei,et al. Oxidative Carbonylierungen: Organometallverbindungen (RM) oder Kohlenwasserstoffe (RH) als Nucleophile , 2011 .
[38] Qiang Liu,et al. Oxidative carbonylation reactions: organometallic compounds (R-M) or hydrocarbons (R-H) as nucleophiles. , 2011, Angewandte Chemie.
[39] Zhiping Li,et al. Selective 1,2-dihalogenation and oxy-1,1-dihalogenation of alkynes by N-halosuccinimides , 2011 .
[40] R. Grigg,et al. Pd-catalysed carbonylations: versatile technology for discovery and process chemists , 2010 .
[41] M. Beller,et al. Recent Applications of Palladium‐Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries , 2009 .
[42] L. McElwee‐White,et al. Preparation of hydantoins by catalytic oxidative carbonylation of alpha-amino amides. , 2009, The Journal of organic chemistry.
[43] M. Beller,et al. Palladiumkatalysierte Carbonylierungen von Arylhalogeniden und ähnlichen Substraten , 2009 .
[44] H. Neumann,et al. Palladium-catalyzed carbonylation reactions of aryl halides and related compounds. , 2009, Angewandte Chemie.
[45] H. Gais. Development of New Methods for Asymmetric Synthesis Based on Sulfoximines , 2007 .
[46] M. Larhed,et al. Ultrafast chemistry: cobalt carbonyl-mediated synthesis of diaryl ketones under microwave irradiation. , 2003, Organic letters.
[47] M. Larhed,et al. Increasing rates and scope of reactions: sluggish amines in microwave-heated aminocarbonylation reactions under air. , 2003, The Journal of organic chemistry.
[48] M. Reggelin,et al. Sulfoximines: Structures, Properties and Synthetic Applications , 2000 .
[49] T. Koenig,et al. Palladium-Catalyzed Hydroarylation of Propiolamides. A Regio- and Stereocontrolled Method for Preparing 3,3-Diarylacrylamides , 1998 .
[50] B. Trost,et al. N-Nitrosulfoximines as Chemical Chameleons for Asymmetric Synthesis , 1992 .
[51] B. Trost. Chemical Chameleons. Organosulfones as Synthetic Building Blocks , 1988 .
[52] Carl R. Johnson. Utilization of sulfoximines and derivatives as reagents for organic synthesis , 1973 .