An Integrated Microreactor for the Multicomponent Synthesis of α-Aminonitriles1
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[1] H. Gröger. Catalytic enantioselective Strecker reactions and analogous syntheses. , 2003, Chemical reviews.
[2] Jeremy L. Steinbacher,et al. Greener approaches to organic synthesis using microreactor technology. , 2007, Chemical reviews.
[3] Peter H Seeberger,et al. Microreactors as tools for synthetic chemists-the chemists' round-bottomed flask of the 21st century? , 2006, Chemistry.
[4] N. Azizi,et al. Lithium Perchlorate Mediated Three‐Component Preparation of α‐Aminonitriles Under Solvent‐Free Conditions , 2004 .
[5] Paul Watts,et al. Continuous Flow Reactors, a Tool for the Modern Synthetic Chemist , 2008 .
[6] A. El-Ahl. A Novel Uncatalyzed Insertion Reaction of In Situ Formed Trichlorosilyl Cyanide with Imines: A Facile Silicon Mediated Synthesis of α-Aminonitriles , 2003 .
[7] A. Strecker. Ueber die künstliche Bildung der Milchsäure und einen neuen, dem Glycocoll homologen Körper; , 1850 .
[8] B. Ranu,et al. Indium trichloride catalyzed one-step synthesis of α-amino nitriles by a three-component condensation of carbonyl compounds, amines and potassium cyanide , 2002 .
[9] L. M. Weinstock,et al. A general synthetic system for 1,2,5-thiadiazoles , 1966 .