Download BarCharts QuickStudy Organic Chemistry Fundamentals by Inc. BarCharts PDF

By Inc. BarCharts

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N. E BUU-Hot,M. D U F O u q F! JACQUIGNON, J. chem. (C)1969 1337. N. €! Buu-Hot, M. MANGANE, E JACQUIGNON, J. Heterocyclic Chem. 7 (1970) 155 Acridon-Synthese JOURDAN-ULLMANN-GOLDBERG durch Cyclisierung von Diphenylamino-o-carbonsauren I mittels Schwefelsaure oder fur viele substituierte Diarylaminocarbonsauren mit Polyphosphorsaure. )hergestellt, die in Gegenwart von Alkalicarbonat und Kupfer erhitzt werden: 18 1. 2. HI Phenylanthranilsaure-Synthese(ULLMANN) H Da die Reaktion wahrscheinlich uber einen nucleophilen Angriff des Arylamin-Stickstoffs auf das halogenierte o-Kohlenstoffatom verlauft, sind sowohl der elektrophile Charakter der o-Chlorbenzoesaure als auch die nucleophile Starke des Amins von Bedeutung fur die Kondensation.

DANIELu. H. SIMON, Liebigs Ann. Chem. 654 (1962) 111. G. KOBRICH,Angew. Chem. 74 (1962) 461. l ! M. POOLE,J. chem. 1963 268. D. M. HALLu. ' D. A. ARCHER, H. BOOTHu. F! C. CRISP,J. chem. Soc. 1964 249. H. J. BESTMANN, H. HABERLEIN u. I. PILS,Tetrahedron 20 (1964) 2079. A. T. BABAYAN u. M. H. INDJIKYAN, Tetrahedron 20 (1964) 1371. u. G. MULLHOFER, Chem. Ber. 97 (1964) 2202. H. SIMON W KIRMSE,Angew. Chem. 77 (1965) 8. L. A. PAQUETTE u. L. D. WISE,J. org. Chemistry 30 (1965) 228. M. A. BALDWIN, D. V BANTHORPE, A.

BURTONu. E I? G. PRAILL,J. chem. SOC. 1950 1203, 2034; 1951 522, 529, 726; 1952 755; 1953 827,837. H. C. BROWNu. , J. Amer. chem. 75 (1953) 6275,6279,6285. Chem. Reviews 52 (1953) 345,352. N. 0. V SONNTAG, G. BADDELEY u. , J. chem. 1954 418; 1956 4647. London) 8 (1954) 355. G. BADDELEY, Quart. Rev. (chem. , I? H. GORE,Chem. Reviews 55 (1955) 229. u. R. N. SHREVE, Ind. Engng. Chem. 48 (1956) 1551. L. E ALBRICHT K. LEROINELSON,Ind. Engng. Chem. 48 (1956) 1670; 49 (1957) 1560. u. G. MARINO, J. Amer.

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