31537-71-0Relevant articles and documents
Photochemically induced cyclization of N-[2-(o-styryl)phenylethyl]acetamides and 5-styryl-1-methyl-1,2,3,4-tetrahydroisoquinolines: New total syntheses of 1-methyl-1,2,3,4-tetrahydronaphtho[2,1-f]isoquinolines
Martínez, Elena,Estévez, Juan C,Estévez, Ramón J,Castedo, Luis
, p. 1981 - 1986 (2007/10/03)
Two new total syntheses of 1-methyl-1,2,3,4-dihydronaphtho[1,2-f]isoquinolines are based on photochemically induced cyclization of N-{2-[(E)-2-phenyl-1-etheynyl]phenylethyl]}acetamides or 1-methyl-5-[(E)-2-phenyl-1-ethenyl]-1,2,3,4-tetrahydroisoquinolines.
Illicit Heroin Manufacturing Byproducts: Copillary Gas Chromatographic Determination and Structural Elucidation of Narcotine- and Norlaudanosine-Related Compounds
Allen, Andrew C.,Cooper, Donald A.,Moore , James M.,Gloger, Manfred,Neumann, Helmut
, p. 2940 - 2947 (2007/10/02)
Capillary gas chromatographic methodology is described for detection of trace quantities of narcotine- and norlaudanosine-related manufacturing impurities in illicit heroin.N-Acetylnornarcotine (2), N-acetylanhydronornarceine (3a,b), 1-acetoxy-N-acetylanhydro-1,9-dihydronornarceine (4a,b),and (E)-3-acrylic acid(5) result from the reaction of narcotine (1) with acetic anhydride.The treatment of norlaudanosine (11a) with acetic anhydride yields N-acetylnorlaudanosine (9).After isolation from thebulk heroin matrix, these impurities, along with morphine, codeine, and thebaine byproducts, are detected by using both fused silica and glass capillary columns in the split mode with flame ionization detection.The syntheses and spectral characterization of these impurities are described.