ISSN 0009-2975
15 papers in the library · publishing 1973-1986
Chemischer Informationsdienst September 30, 1986 D. Dauzonne, R. Royer
New precursors (III) of mescaline analogs are prepared by condensing trimethoxy-conitroethylbenzene (I) with aromatic aldehydes (II).
Chemischer Informationsdienst May 28, 1985 L. J. Iii Valdes, W. M. Butler, G. M. Hatfield et al.
Divinorin A (Ia) is the first terpenoid clearly recognized as a gsxchoo trop, and Divinorin B, both from the mint plant Salvia divinorum (Mexican mint), are confirmed in terms of their structures.
Chemischer Informationsdienst November 27, 1984 P. Iii Jacob, A. T. Shulgin
No Summary
Chemischer Informationsdienst August 30, 1983 M. W. Majchrzak, A. Kotelko, R. Guryn et al.
No Summary
Chemischer Informationsdienst April 20, 1982 P. Iii Jacob, A. T. Shulgin
No Summary
Chemischer Informationsdienst August 21, 1979 A. M. Kadry, Y. A. Ibrahim, K. M. Ghoneim et al.
Starting from trihydroxybenzoic acid (I), the mescaline derivative (IX) is prepared via the route shown in the reaction scheme.
Chemischer Informationsdienst December 26, 1978 R. A. Glennon, S. M. Liebowitz, E. C. Mack
No Summary
Chemischer Informationsdienst January 10, 1978 Y. Nakahara, T. Niwaguchi, H. Ishii
Hydrogenation of LSD (I) with hydrogen over palladium on carbon yields dihydrolysergic acid diethylamide (II), whereas hydrogenation of iso-LSD (III) gives a mixture of the dihydro compounds (IV) and (V).
Chemischer Informationsdienst July 5, 1977 D. E. Nichols, D. C. Dyer
No Summary
Chemischer Informationsdienst March 15, 1977 F. Jun. Desantis, K. A. Nieforth
No Summary
Chemischer Informationsdienst October 26, 1976 T. Niwaguchi, Y. Nakahara, H. Ishii
No Summary
Chemischer Informationsdienst March 30, 1976 A. T. Shulgin, D. C. Dyer
Unlocking secrets of brain chemistry is crucial. Scientists successfully synthesized a new class of molecules, derived from simpler structures, hypothesized to mimic certain brain states. This chemical creation provides valuable tools, offering positive insights into how molecular design influences psychoactive effects and expanding our understanding of brain function.
Chemischer Informationsdienst January 14, 1975 R. J. Wolters, A. J. Bej, N. S. Tanner
A chemical reaction converts 3,4,5-trimethoxyphenylacetonitrile (I) with bromopropionitrile in the presence of sodium hydride in dimethylformamide to yield a glutaronitrile derivative (II) in 50% yield. Subsequent alkaline hydrolysis of (II) produces a glutaric acid derivative (III) in 77% yield.
Chemischer Informationsdienst August 20, 1974 Y. Nakahara, T. Niwaguchi
Amidation of lysergic acid (I) using triphenyl phosphite/imidazole/phosphoric acid tris-(dimethylamide) or phosphoric acid tris-(dimethylamide)/tosyl chloride yields compounds (II) and (III). With the latter reagent, compounds (II) are obtained in 68-75% yield and compounds (III) in up to 3-8% yield.
Chemischer Informationsdienst December 18, 1973 P. D. Cooper
No Summary