249. Massenspektrometrie und ihre Anwendung auf strukturelle und stereochemische Probleme CXXI [1]. Fragmentierungen und Wasserstoffverschiebungen in 4‐Keto‐androstanen
暂无分享,去创建一个
[1] C. Djerassi,et al. Mass Spectrometry in Structural and Stereochemical Problems. XCIII.1 Further Observations on the Importance of Interatomic Distance in the McLafferty Rearrangement. Synthesis and Fragmentation Behavior of Deuterium-Labeled 12-Keto Steroids2,3 , 1966 .
[2] H. Budzikiewicz,et al. Massenspektroskopie und ihre Anwendung auf strukturelle und stereochemische Probleme, LXXVII. Einfluß behinderter Rotation sowie anderer energetischer Faktoren auf die McLafferty‐Umlagerung von Ketonen , 1966 .
[3] C. Djerassi,et al. Mass spectrometry in structural and stereochemical problems. LXXXI. Stereospecificity in a hydrogen-transfer reaction characteristic of 6-keto steroids. , 1965, Journal of the American Chemical Society.
[4] John D. Roberts,et al. Conformational Barriers in Medium-Sized Rings. I. trans-Cyclodecene-1,2,4,4,9,9-d_6 , 1965 .
[5] C. Djerassi,et al. Mass Spectrometry in Structural and Stereochemical Problems. LXV.1 Synthesis and Fragmentation Behavior of 15-Keto Steroids. The Importance of Interatomic Distance in the McLafferty Rearrangement2 , 1965 .
[6] P. Stang,et al. A CONVENIENT PREPARATION OF METHANOL-d , 1964 .
[7] C. Djerassi,et al. Mass Spectrometry in Structural and Sterochemical Probelms. L.1Fragmentation and Hydrogen Migration Reactions of α,β-Unsaturated 3-Keto Steroids2 , 1964 .
[8] Y. Mazur,et al. The Hydration of Unsaturated Steroids by the Brown Hydroboration Reaction. I. Monounsaturated Steroids , 1964 .
[9] C. Djerassi,et al. Unusual Chemical Shifts in the Nuclear Magnetic Resonance Spectra of 7- and 11-Keto Steroids , 1963 .
[10] C. Djerassi,et al. The introduction of deuterium into the C-19 angular methyl group , 1963 .
[11] C. Djerassi,et al. Mass Spectrometry in Structural and Stereochemical Problems. I. Steroid Ketones , 1962 .
[12] H. Brown,et al. THE CHROMIC ACID OXIDATION OF ORGANOBORANES—A CONVENIENT PROCEDURE FOR CONVERTING OLEFINS INTO KETONES via HYDROBORATION , 1961 .
[13] C. Djerassi,et al. Relative Stabilities of cis and trans Isomers. VIII.1a Optical Rotatory Dispersion Studies. XXXIV.1b Kinetic and Equilibrium Measurements on Some Steroidal Hydrindanones , 1960 .
[14] C. Djerassi,et al. Optical Rotatory Dispersion Studies. XVI.1 Synthesis and Conformation of Optically Active Octalones and Decalones2 , 1958 .
[15] A. Meyer. FORMATION OF 6α, 1 1β-DIHYDROXY-Δ4-ANDROSTENE3,17-DIONE AND OTHER C19-COMPOUNDS BY A COW ADRENAL HOMOGENATE PREPARATION , 1957 .
[16] L. Fieser,et al. Rearrangement of 6β-Bromo-Δ4-cholestene-3-one to 2α-Acetoxy-Δ4-cholestene-3-one1 , 1953 .
[17] C. Djerassi,et al. Steroidal Sapogenins. XX.1a Synthesis and Reactions of the Epimeric Δ5-22-Isospirosten-3β,7-diols1b , 1952 .
[18] A. Butenandt,et al. Über die Konstitution der Lumisteroide , 1952 .
[19] C. Djerassi. The method of molecular rotation differences applied to 3-keto steroids of the allo series. , 1947, The Journal of organic chemistry.
[20] P. Wieland,et al. Steroide und Sexualhormone. (113. Mitteilung). Untersuchungen über den Zusammenhang zwischen Konstitution und Geruch bei Steroiden , 1945 .