Additions and Corrections - Steroids with a Glyoxal Side Chain at C-17 and RElated Compounds

1951 ◽  
Vol 16 (12) ◽  
pp. 1932-1932
Author(s):  
Gerard Fleisher ◽  
Edward Kendall
Keyword(s):  
Author(s):  
Rudolph A. Abramovitch ◽  
Dorota A. Abramovitch ◽  
Piotr Tomasik
Keyword(s):  

1980 ◽  
Vol 11 (9) ◽  
Author(s):  
R. A. ABRAMOVITCH ◽  
D. A. ABRAMOVITCH ◽  
P. TOMASIK
Keyword(s):  

Heterocycles ◽  
1985 ◽  
Vol 23 (11) ◽  
pp. 2843 ◽  
Author(s):  
Csaba Szántay ◽  
M�ia Incze ◽  
Ferenc S葉i ◽  
Zsuzsanna Kardos-Balogh

2013 ◽  
Vol 8 (6) ◽  
pp. 1934578X1300800
Author(s):  
Pinus Jumaryatno ◽  
Lynette K. Lambert ◽  
John N. A. Hooper ◽  
Joanne T. Blanchfield ◽  
Mary J. Garson

A cyclic peroxide 1 with an unusual phenethenyl side chain, together with the known peroxide 2 with a C4-sidechain have been isolated from a two-sponge association of Plakortis communis – Agelas mauritiana (Carter, 1883) collected near Mooloolaba, South-East Queensland, Australia. Metabolite purification was complicated by the presence of the free carboxylic acid groups in 1 and 2; therefore, diazomethane treatment was undertaken to afford methyl ester 3. Following RP-HPLC purification, the ring-opened analogues 4 and 5 were also obtained. The structures of the new compounds were elucidated on the basis of their 1D and 2D NMR and MS data, and by comparison with literature data. The relative configuration of the isolated peroxides was determined by the interpretation of JH-H values and comparison of the 13C chemical shift data with literature data for related compounds. The bromopyrrole alkaloid longamide (6) was also isolated.


1960 ◽  
Vol 38 (4) ◽  
pp. 554-556 ◽  
Author(s):  
R. A. Abramovitch ◽  
J. M. Muchowski

The scope of the tryptamine synthesis via 1-oxo-1,2,3,4-tetrahydro-β-carbolines has been extended to tryptamines bearing a side-chain α-alkyl group. The preparation of 3-(2-amino-1-methylethyl)indole by this procedure is described.


1977 ◽  
Vol 23 (2) ◽  
pp. 169-174 ◽  
Author(s):  
W A Ratcliffe ◽  
S M Fletcher ◽  
A C Moffat ◽  
J G Ratcliffe ◽  
W A Harland ◽  
...  

Abstract We raised high-titre antisera to two LSD-bovine serum albumin conjugates, one linked via the indole nitrogen, the other via the amide side-chain. The antisera were specific for different parts of the LSD molecule, as demonstrated by cross-reactivity studies with LSD, its metabolites, ergot alkoloids, and closely related compounds. The antisera were used to develop a double-antibody radioimmunoassay with a detection limit of about 0.4 mug of LSD per liter of unextracted urine or serum. We saw no nonspecific interference by urine, serum, or from a series of commonly used drugs. There was good correlation between immunoassay values obtained with the two antisera (r = 0.91). However, the antiserum linked via the indole nitrogen gave consistently higher results for samples from persons who had taken LSD, owing to greater cross-reactivity with LSD metabolites. Radioimmunoassay by use of two such antisera is a more specific screening procedure for LSD abuse than has been available previously. In addition, antisera cross-reacting with LSD metabolites allow measurement of these compounds, for which there is no satisfactory method at the concentrations found in biological fluids in man.


1971 ◽  
Vol 49 (19) ◽  
pp. 3143-3151 ◽  
Author(s):  
K. Bailey ◽  
A. W. By ◽  
K. C. Graham ◽  
D. Verner

Data from the p.m.r. spectra of β-amino-, β-aminohydrochloride-, β-hydroxy-, and β-nitro-α-phenyl-propanes having methyl or methoxy substituants on the phenyl ring (37 compounds in all) are presented. The α and β protons of the side-chain give a pattern usually analyzable as ABX. The data are discussed in terms of correlations of coupling constants and chemical shifts with electronegativity of the substituent groups, steric and electronic effects, and apparent changes in rotamer populations. Hydrogen-bonding between the amino group of amphetamines and a methoxyl function at the ortho position in the phenyl ring is indicated for the salts but not the free bases.


1985 ◽  
Vol 38 (3) ◽  
pp. 467 ◽  
Author(s):  
DJ Brown ◽  
K Mori

Synthetic routes are described to a series of 2-, 6- and 8- phenylpurines , each with an appropriate S-or NH-linked side chain elsewhere in the molecule; to 2- and 4-phenylpteridines, each with a similar side chain and some with two additional C-methyl groups, to 2- and 4-phenylquinazolines, each equipped with an analogous side chain; and to two pyridinyl analogues of the above. Three of the above components are shown to have considerable activity as amplifiers of phleomycin -G in an in vitro bacterial system.


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