Approach to synthesis of 8-azasteroids: Communication 1. Synthesis and some properties of benzo[a]cycloalkano[f]quinolizines

[1]  A. Meyers,et al.  Azasteroids. IX. Synthesis and stereochemistry of 12-oxo-17-deoxo-8-azaestrone methyl ether , 1970 .

[2]  K. Friedrich.  Herstellung von Bicyclo[3.1.0]hexandion-(2,4) , 1970 .

[3]  A. Meyers,et al.  Chemistry of cyclic enamino ketones. IV. Factors affecting carbon and oxygen alkylation , 1969 .

[4]  J. Shavel,et al.  Azecino[2,1-.alpha.]tetrahydroisoquinolines and related compounds. I. Reaction of 3,4-dihydroisoquinolines with nonenolizable .beta.-diketones , 1968 .

[5]  L. Ehrenberg,et al.  2-Acylcyclopentane-1,3-diones. , 1967 .

[6]  A. Meyers,et al.  Azasteroids—VI : A facile total synthesis of dl-8-azaestrone methyl ether and related systems , 1967 .

[7]  J. Shavel,et al.  A New General Synthesis of Benzo[a]quinolizines, Dibenzo[a, f]quinolizines, and Related Compounds , 1966 .

[8]  J. Weisbach,et al.  alkaloids structure and stereochemistry of the major alkaloids of and , 1966 .

[9]  W. Sobotka,et al.  Azasteroids. V. The Direct Conversion of 1-(Carboethoxymethyl)-1,2,3,4-tetrahydroisoquinolines and Cyclic Ketones into Benzo[a]cycloalkano[f]quinolizinones. An Example of Enamine Acylation by an Ester Function1,2 , 1965 .

[10]  W. Sobotka,et al.  A versatile approach to the 8- and 9-azasteroid system. Angular methylation at C-10 and C-13′ , 1965 .

[11]  A. Brossi,et al.  The Nuclear Magnetic Resonance Spectra of the Angular Proton in Benzo[a]- and Indolo[a]quinolizidines , 1964 .

[12]  S. Forsén,et al.  Spectroscopic Studies on Enols. Part 7. NMR and IR Investigations of Hydrogen Bonding and Tautomerism in Cyclopentane Enols. , 1964 .

[13]  W. J. Dale,et al.  Substituted Styrenes. VI. Syntheses of the Isomeric Formylstyrenes and o- and m-Vinylbenzoic Acid , 1961 .

[14]  M. Karplus.  Contact Electron‐Spin Coupling of Nuclear Magnetic Moments , 1959 .

[15]  H. Smith.  165. 2-Acetylcyclohexane-1 : 3-dione , 1953 .

[16]  W. Dieckmann,et al.  Ueber das Verhalten von 1.3-Dicarbonylverbindungen gegen Essigsäureanhydrid und über die Acetylderivate des Dimethyl- und Phenyl-Hydroresorcins , 1904 .