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Total syntheses of the bilirubin oxidation end product Z-BOX C and its isomeric form Z-BOX D. Daniel Schulze, Juliane Traber, Marcel Ritter, Helmar Görls, Georg Pohnert, Matthias Westerhausen , Org. Biomol. Chem. , 2019 , 17 , 6489

An efficient method for the synthesis of unsymmetrical 2,2′-bis(pyrrolyl)alkanes. Marie Laure Murat-Onana, Christophe Berini, Frédéric Minassian, Nadia Pelloux-Léon, Jean-Noël Denis , Org. Biomol. Chem. , 2010 , 8 , 2204

First catalyst-free CO2 trapping of N-acyliminium ions under ambient conditions: sustainable multicomponent synthesis of thia- and oxazolidinyl carbamates. Max Franz, Timo Stalling, Henning Steinert, Jürgen Martens , Org. Biomol. Chem. , 2018 , 16 , 8292

Organic chemistry , J. Chem. Soc., Abstr. , 1905 , 88 , A557

55. Acetyl chloride as a polar solvent. Part I. Solubility of substances and formation of solvates in acetyl chloride. Ram Chand Paul, Dula Singh, Sarjit Singh Sandhu , J. Chem. Soc. , 1959 , 315

In situ spectroscopic studies related to the mechanism of the Friedel–Crafts acetylation of benzene in ionic liquids using AlCl3 and FeCl3. Szilárd Csihony, Hasan Mehdi, Zoltán Homonnay, Attila Vértes, Ödön Farkas, István T. Horváth , J. Chem. Soc., Dalton Trans. , 2002 , 680

Photolysis of acetyl chloride. W. D. Capey, J. R. Majer, J. C. Robb , J. Chem. Soc. B , 1968 , 447

Structure-activity evaluation of new uracil-based non-nucleoside inhibitors of HIV reverse transcriptase. Elena S. Matyugina, Vladimir T. Valuev-Elliston, Alexander N. Geisman, Mikhail S. Novikov, Alexander O. Chizhov, Sergey N. Kochetkov, Katherine L. Seley-Radtke, Anastasia L. Khandazhinskaya , Med. Chem. Commun. , 2013 , 4 , 1443

Hydration thermodynamics of aliphatic alcohols. Giuseppe Graziano , Phys. Chem. Chem. Phys. , 1999 , 1 , 3567

A facile synthesis of dispersable NaCl nanocrystals. Thomas Annen, Matthias Epple , Dalton Trans. , 2009 , 9731