Synthesis of Tetrahydroisoindolinones via a Metal‐Free Dehydrogenative Diels‐Alder Reaction

[1]  Hui Yang,et al.  Metal-Free Dehydrogenative Diels-Alder Reactions of Prenyl Derivatives with Dienophiles via a Thermal Reversible Process. , 2018, Organic letters.

[2]  B. Jiang,et al.  Copper-Catalyzed Dehydrogenative Diels-Alder Reaction. , 2018, Organic letters.

[3]  Xiang Wu,et al.  An Asymmetric Dehydrogenative Diels-Alder Reaction for the Synthesis of Chiral Tetrahydrocarbazole Derivatives. , 2018, Organic letters.

[4]  Guigen Li,et al.  Cobalt-Catalyzed Cross-Dehydrogenative Coupling Reaction between Unactivated C(sp2)-H and C(sp3)-H Bonds. , 2017, Organic letters.

[5]  A. Antonchick,et al.  A Metal-Free Oxidative Dehydrogenative Diels-Alder Reaction for Selective Functionalization of Alkylbenzenes. , 2017, Chemistry.

[6]  M. G. Medvedev,et al.  Quantifying Possible Routes for SpnF-Catalyzed Formal Diels-Alder Cycloaddition. , 2017, Journal of the American Chemical Society.

[7]  R. Butcher,et al.  Synthesis, spectral characterization, and evaluation of antimicrobial activity of O,O′-alkanediyl S-(N-phthalimidomethyl) dithiophosphates and zinc bis(O,O′-alkanediyl) dithiophosphates , 2017 .

[8]  Koichi Tanaka,et al.  Enantioselective Diels–Alder reaction in the confined space of homochiral metal–organic frameworks , 2016 .

[9]  Paramjit Singh,et al.  Cross Dehydrogenative Coupling (CDC) Reactions of N,N-Disubstituted Formamides, Benzaldehydes and Cycloalkanes , 2016 .

[10]  Veerababurao Kavala,et al.  Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile. , 2016, Chemical communications.

[11]  Changwei Hu,et al.  Unique Steric Effect of Geminal Bis(silane) To Control the High Exo-selectivity in Intermolecular Diels-Alder Reaction. , 2016, Journal of the American Chemical Society.

[12]  Junliang Zhang,et al.  Recent Progress in Dehydro(genative) Diels-Alder Reaction. , 2016, Chemistry.

[13]  Junliang Zhang,et al.  Metal‐Free Dehydrogenative Diels—Alder Reactions of 2‐Methyl‐3‐alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes. , 2015 .

[14]  Ling Zhou,et al.  A Dehydrogenative Diels–Alder Reaction of Prenyl Derivatives with 2,3‐Dichloro‐5,6‐dicyanobenzoquinone , 2015 .

[15]  C. Thirunavukkarasu,et al.  Synthesis and biological evaluation of isoindoloisoquinolinone, pyroloisoquinolinone and benzoquinazolinone derivatives as poly(ADP-ribose) polymerase-1 inhibitors. , 2015, Bioorganic & medicinal chemistry.

[16]  A. Saikia,et al.  Stereoselective synthesis of amido and phenyl azabicyclic derivatives via a tandem aza Prins-Ritter/Friedel-Crafts type reaction of endocyclic N-acyliminium ions. , 2013, The Journal of organic chemistry.

[17]  Katharine J. Cahill,et al.  Biomimetic dehydrogenative Diels-Alder cycloadditions: total syntheses of brosimones A and B. , 2013, Angewandte Chemie.

[18]  Xianxing Jiang,et al.  Recent developments in catalytic asymmetric inverse-electron-demand Diels-Alder reaction. , 2013, Chemical reviews.

[19]  Ying‐Chun Chen,et al.  Aminocatalytic asymmetric Diels-Alder reactions via HOMO activation. , 2012, Accounts of chemical research.

[20]  Rai‐Shung Liu,et al.  Gold-catalyzed isomerization of unactivated allenes into 1,3-dienes under ambient conditions. , 2012, Chemical communications.

[21]  M. Beller,et al.  Selective Catalytic Monoreduction of Phthalimides and Imidazolidine-2,4-diones. , 2012 .

[22]  M. White,et al.  Molecular complexity via C-H activation: a dehydrogenative Diels-Alder reaction. , 2011, Journal of the American Chemical Society.

[23]  D. MacMillan,et al.  Collective synthesis of natural products by means of organocascade catalysis , 2011, Nature.

[24]  J. Muzart,et al.  Intermolecular dehydrogenative Heck reactions. , 2011, Chemical reviews.

[25]  C. Yeung,et al.  Catalytic dehydrogenative cross-coupling: forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds. , 2011, Chemical reviews.

[26]  C. Su,et al.  Study on synthesis of thalidomide analogues and their bioactivities; inhibition on iNOS pathway and cytotoxic effects , 2011, Medicinal Chemistry Research.

[27]  A. Lei,et al.  Bond formations between two nucleophiles: transition metal catalyzed oxidative cross-coupling reactions. , 2011, Chemical reviews.

[28]  S. Bergens,et al.  Desymmetrization of meso-cyclic imides via enantioselective monohydrogenation. , 2010, Journal of the American Chemical Society.

[29]  Dale L Boger,et al.  Total synthesis and evaluation of a key series of C5-substituted vinblastine derivatives. , 2010, Journal of the American Chemical Society.

[30]  Caroline J. Scheuermann Beyond traditional cross couplings: the scope of the cross dehydrogenative coupling reaction. , 2010, Chemistry, an Asian journal.

[31]  S. Kim,et al.  Tandem Diels-Alder/cross-coupling reactions of generated in situ organoindium reagents in a one-pot process. , 2010, Organic letters.

[32]  J. Ashenhurst Intermolecular oxidative cross-coupling of arenes. , 2010, Chemical Society reviews.

[33]  E. Corey,et al.  Highly enantioselective Diels-Alder reactions of maleimides catalyzed by activated chiral oxazaborolidines. , 2010, Organic letters.

[34]  A. Kapdi,et al.  Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage. , 2009, Angewandte Chemie.

[35]  A. V. Varlamov,et al.  A new approach to construction of isoindolo[1,2-a]isoquinoline alkaloids Nuevamine, Jamtine, and Hirsutine via IMDAF reaction , 2009 .

[36]  Herbert Waldmann,et al.  Synthesis of natural product inspired compound collections. , 2009, Angewandte Chemie.

[37]  Chao‐Jun Li Cross-dehydrogenative coupling (CDC): exploring C-C bond formations beyond functional group transformations. , 2009, Accounts of chemical research.

[38]  P. Wessig,et al.  The dehydro-Diels-Alder reaction. , 2008, Chemical reviews.

[39]  T. Lübbers,et al.  Design, synthesis, and structure-activity relationship studies of new phenolic DNA gyrase inhibitors. , 2007, Bioorganic & medicinal chemistry letters.

[40]  D. Newman,et al.  Natural products as sources of new drugs over the last 25 years. , 2007, Journal of natural products.

[41]  C. Day,et al.  Preparation of 2-trialkylsiloxy- substituted 1,3-dienes and their diels-alder/cross-coupling reactions. , 2005, Organic letters.

[42]  Luigi Vaccaro,et al.  [AlCl3 + 2THF]: A New and Efficient Catalytic System for Diels−Alder Cycloaddition of α,β-Unsaturated Carbonyl Compounds under Solvent-Free Conditions , 2006 .

[43]  R. Varma,et al.  Aqueous N-heterocyclization of primary amines and hydrazines with dihalides: microwave-assisted syntheses of N-azacycloalkanes, isoindole, pyrazole, pyrazolidine, and phthalazine derivatives. , 2006, The Journal of organic chemistry.

[44]  A. Padwa,et al.  The Pummerer reaction: methodology and strategy for the synthesis of heterocyclic compounds. , 2004, Chemical reviews.

[45]  Koichi Tanaka,et al.  Preparation of optically active cis-4-methylcyclohex-4-ene-1,2-dicarboximides by a combination of Diels–Alder reaction and complexation with optically active hosts and enantioselective Diels–Alder reaction in inclusion crystals in a water suspension medium , 2003 .

[46]  E. Corey Catalytic enantioselective Diels--Alder reactions: methods, mechanistic fundamentals, pathways, and applications. , 2002, Angewandte Chemie.

[47]  D. MacMillan,et al.  The First General Enantioselective Catalytic Diels−Alder Reaction with Simple α,β-Unsaturated Ketones , 2002 .

[48]  E. Corey,et al.  The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters. , 1998, Angewandte Chemie.

[49]  K. Peters,et al.  Highly Like-Selective [4 + 2] Cycloadditions of Chiral Dienols: The Importance of 1,3-Allylic Strain in the Hydroxy-Directed Stereocontrol , 1995 .

[50]  K. Dulak,et al.  Determination of phosmet by high-performance liquid chromatography. , 1987, Journal of chromatography.

[51]  O. Diels,et al.  Synthesen in der hydroaromatischen Reihe, VI. Mitteilung, Kurt Alder und Gerhard Stein: Über partiell hydrierte Naphtho‐ und Anthrachinone mit Wasserstoff in γ‐ bzw. δ‐Stellung. (Mitbearbeitet von Paul Pries und Hans Winckler) , 1929 .