Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1965, 30, 2125-2127
https://doi.org/10.1135/cccc19652125

Note on the formylation of chloro- and bromoacetic acid

Z. Arnold

Crossref Cited-by Linking

  • Lu Qiuyu, He Wei, Sun Wen, Feng Ye, Zhan Li, Luo Yu: Synthesis of 2-arylamino-5-formyl-pyrimidines from the bis(hexafluorophosphate) Arnold salt. Journal of Chemical Research 2020, 44, 580. <https://doi.org/10.1177/1747519820911271>
  • Szennyes Eszter, Gyémánt Gyöngyi, Somsák László, Bokor Éva: Synthesis of New Series of 2-C-(β-D-glucopyranosyl)-Pyrimidines and Their Evaluation as Inhibitors of Some Glycoenzymes. Molecules 2020, 25, 701. <https://doi.org/10.3390/molecules25030701>
  • Reber Keith P., Burdge Hannah E.: Synthesis and Applications of Tricarbonylmethane Compounds. Organic Preparations and Procedures International 2018, 50, 2. <https://doi.org/10.1080/00304948.2018.1405332>
  • Su Weike, Weng Yiyi, Sun Chen, Cao Qingwei, Chen Hantao, Li Nanhui, Chen Zhuo: New Facile Synthesis of 3-Substituted 7,8-Dihydroquinolin-5(6H)-ones and [1]Benzopyrano[4,3-b]pyridin-5-ones Using 2-(Hetero)arylvinamidinium Salts. HETEROCYCLES 2018, 96, 1889. <https://doi.org/10.3987/COM-18-13988>
  • Maltsev Oleg V., Rausch Rodger, Quan Zheng‐Jun, Hintermann Lukas: Synthesis of Soai Type 2‐Arylpyrimidine‐5‐carbaldehydes through Desulfurative Cross‐Coupling with Arylboronic Acids. Eur J Org Chem 2014, 2014, 7426. <https://doi.org/10.1002/ejoc.201403133>
  • Maltsev Oleg V., Pöthig Alexander, Hintermann Lukas: Synthesis of Soai Aldehydes for Asymmetric Autocatalysis by Desulfurative Cross-Coupling. Org. Lett. 2014, 16, 1282. <https://doi.org/10.1021/ol500189s>
  • Jameleddine Khiari, Adnen Hadj Ayed Med, Béchir Ben Hassine: An efficient preparation and some reactions of 2-dimethylaminomethylene-1,3-bis(dimethylimonio)propane diperchlorate. Tetrahedron Letters 2006, 47, 2973. <https://doi.org/10.1016/j.tetlet.2006.02.101>
  • Wolff J. Jens, Wortmann R�diger: Organic Materials for Non-Linear Optics: The 2D Approach. J. Prakt. Chem. 1998, 340, 99. <https://doi.org/10.1002/prac.19983400202>
  • Wortmann Rüdiger, Glania Christoph, Krämer Peter, Matschiner Ralf, Jens Wolff J., Kraft Stefan, Treptow Björn, Barbu Eugen, Längle Daniela, Görlitz Gunter: Nondipolar Structures With Threefold Symmetry For Nonlinear Optics. Chemistry A European J 1997, 3, 1765. <https://doi.org/10.1002/chem.19970031107>
  • Gompper Rudolf, Walther Peter, Bräuchle Christoph, Stadler Stefan: Chemistry and nonlinear optical properties of new 2H-benzotriazole derivatives. Tetrahedron 1996, 52, 14607. <https://doi.org/10.1016/0040-4020(96)00895-2>
  • Krasnaya Zhanna A., Smirnova Yuliya V., Krystal Galina V., Bogdanov Valentin S.: Aminaleacetal of dimethylaminomethylenemalonaldehyde – a novel reagent for the synthesis of substituted aminopolyenes. Mendeleev Communications 1996, 6, 17. <https://doi.org/10.1070/MC1996v006n01ABEH000558>
  • Reichardt Christian, Budnik Ulrich, Harms Klaus, Schäfer Gerhard, Stein Jörg: Chiral polymethine dyes, V. syntheses, absolute configuration, spectroscopic, and chiroptical properties of chiral dinuclear tri‐ and pentamethinium as well as trinuclear [2.2.2]heptamethinediium cyanine dyes with 3‐sec‐butyl‐1,3‐dimethylindolyl end groups. Liebigs Ann./Recl. 1995, 1995, 329. <https://doi.org/10.1002/jlac.199519950241>
  • Troschütz Reinhard, Dennstedt Thomas: Synthese von substituierten 2‐Aminonicotinonitrilen. Archiv der Pharmazie 1994, 327, 33. <https://doi.org/10.1002/ardp.19943270107>
  • Marson Charles M.: Reactions of carbonyl compounds with (monohalo) methyleniminium salts (vilsmeier reagents). Tetrahedron 1992, 48, 3659. <https://doi.org/10.1016/S0040-4020(01)92263-X>
  • Gupton John T., Gall John E., Riesinger Steve W., Smith Stanton Q., Bevirt Kathy M., Sikorski James A., Dahl Maria L., Arnold Zdenek: An alternative preparation of the 2‐dimethylaminomethylene‐1,3‐bis(dimethylimmonio)propane salt from phosphonoacetic acids and some applications in heterocyclic synthesis. Journal of Heterocyclic Chem 1991, 28, 1281. <https://doi.org/10.1002/jhet.5570280520>
  • Yanovskaya L. A., Kryshtal' G. V.: Methylenemalonic aldehydes and their use in organic synthesis (review). Chem Heterocycl Compd 1991, 27, 807. <https://doi.org/10.1007/BF00472275>
  • Adams Florian, Gompper Rudolf: Di(4‐pyridinio)‐, Di(2‐benzothiazolio)‐, Di(2‐[1,3‐dithiolylio])‐ und Diformyl‐tetraaza[14]annulene sowie Tetraaza[14]annulenylen‐homologe Tetrathiafulvalene. Angewandte Chemie 1989, 101, 1046. <https://doi.org/10.1002/ange.19891010814>
  • Adams Florian, Gompper Rudolf: Di(4‐pyridinio)‐, Di(2‐benzothiazolio)‐, Di(2‐[1,3‐dithiolylio])‐ and Diformyltetraaza[14]annulenes and Tetraaza[14]annulenylene‐Homologous Tetrathiafulvalenes. Angew. Chem. Int. Ed. Engl. 1989, 28, 1063. <https://doi.org/10.1002/anie.198910631>
  • Frissen A.E., Marcelis A.T.M., Geurtsen G., de Bie D.A., van der Plas H.C.: Intramolecular Diels-Alder reactions of 2-(alkynyl)pyrimidines and 2-(alkynyl)pyridines. Tetrahedron 1989, 45, 5151. <https://doi.org/10.1016/S0040-4020(01)81093-0>
  • Arnold Z., Kryshtal G.V., Král V., Dvorˇák D., Yanovskaya L.A.: The first general synthetic approach to aikylidenemalonaldehydes. Tetrahedron Letters 1988, 29, 2861. <https://doi.org/10.1016/0040-4039(88)85231-6>
  • Adams Florian, Gompper Rudolf, Hohenester Achim, Wagner Hans-Ulrich: Y-aromatic dications and stabilized trimethylenemethanes. Tetrahedron Letters 1988, 29, 6921. <https://doi.org/10.1016/S0040-4039(00)88475-0>
  • Knorr Rudolf, Ruf Friedrich, Högerl Johann, Hilpert Monika, Hassel Petra: (1‐Alkoxyalkyl)malonaldehyd‐dianile. aus Formylmalonaldehyd‐dianil durch Aldimin‐Reduktion und 1,3‐Anilin‐Verschiebung. Chem. Ber. 1985, 118, 4743. <https://doi.org/10.1002/cber.19851181209>
  • Ruf Friedrich, Högerl Johann, Knorr Rudolf, Bronberger Hildegard: (1‐Alkenyl)malonaldehyd‐dianile aus Formylmalonaldehyd‐dianil. Chem. Ber. 1985, 118, 4754. <https://doi.org/10.1002/cber.19851181210>
  • Reichardt Christian, Knecht Josef, Morsek Walter, Plaas Dietrich, Allmann Rudolf, Kucharczyk Damian: Synthesen mit aliphatischen Dialdehyden, XXXVII. Darstellung, Struktur und Eigenschaften eines [3.3.3]Decamethinium‐Cyaninfarbstoffes mit Indolin‐Endgruppen. Chem. Ber. 1983, 116, 1982. <https://doi.org/10.1002/cber.19831160525>
  • Knorr Rudolf, Weiß Alfons: Synthesen und Eigenschaften hochsubstituierter Vinamidine. Chem. Ber. 1982, 115, 139. <https://doi.org/10.1002/cber.19821150115>
  • Ren Iwata, Tatsuo Ido, Takeshi Tominaga: The production of 11C-guanidine by the proton irradiation of the liquid ammonia-nitrous oxide system and its use in the synthesis of 11C-pyrimidines. The International Journal of Applied Radiation and Isotopes 1981, 32, 303. <https://doi.org/10.1016/0020-708X(81)90090-9>
  • Lloyd Douglas, McNab Hamish: Vinamidine und Vinamidiniumsalze — Beispiele stabilisierter Push‐Pull‐Alkene. Angewandte Chemie 1976, 88, 496. <https://doi.org/10.1002/ange.19760881503>
  • Lloyd Douglas, McNab Hamish: Vinamidines and Vinamidinium Salts—Examples of Stabilized Push‐Pull Alkenes. Angew. Chem. Int. Ed. Engl. 1976, 15, 459. <https://doi.org/10.1002/anie.197604591>
  • Reichardt Christian, Halbritter Klaus: Darstellung, Struktur und Reaktionen der Halogenmalondialdehyde. Angewandte Chemie 1975, 87, 124. <https://doi.org/10.1002/ange.19750870403>
  • Reichardt Christian, Halbritter Klaus: Preparation, Structure, and Reactions of Halomalondialehdes. Angew. Chem. Int. Ed. Engl. 1975, 14, 86. <https://doi.org/10.1002/anie.197500861>
  • Jutz Christian, Wagner Rudolf M.: Die synchrone Sechs‐Elektronen‐Cyclisierung von Hexatrien‐Systemen als neues Syntheseprinzip zur Darstellung von Aromaten und Heteroaromaten. Angewandte Chemie 1972, 84, 299. <https://doi.org/10.1002/ange.19720840714>
  • Jutz Christian, Wagner Rudolph M.: Synchronous Six‐Electron Cyclization of Hexatriene Systems as a New Synthetic Principle for Preparation of Aromatic and Heteroaromatic Compounds. Angew. Chem. Int. Ed. Engl. 1972, 11, 315. <https://doi.org/10.1002/anie.197203151>
  • Wagner Rudolf M., Jutz Christian: Umsetzung von vinylogen Formamidinium‐Salzen mit Nucleophilen. I Eine Variante der Pyrimidin‐Synthese. Chem. Ber. 1971, 104, 2975. <https://doi.org/10.1002/cber.19711041002>
  • Jutz Christian, Kirchlechner Richard, Seidel Hans‐Jürgen: Über die Umsetzung von Phenalen mit vinylogen Formamidinium‐Salzen: Synthese substituierter Pyrene und des Azuleno[5.6.7‐cd]phenalens. Chem. Ber. 1969, 102, 2301. <https://doi.org/10.1002/cber.19691020719>
  • Reichardt Chr.: Synthesen mit substituierten malondialdehyden III trinucleare pentamethincyanin-farbstoffe. Tetrahedron Letters 1967, 8, 4327. <https://doi.org/10.1016/S0040-4039(01)89684-2>