Biomedical subjects

P L Ruddock

Publications and source records attributed to P L Ruddock.

3 recordsLinked to original sources

PubMed1999

The effect of 4beta and 19 ester functionalities on some electrophilic addition reactions of delta5-steroids.

The reactions of 3beta-acyloxyandrost-5-enes with bromine/silver acetate (Petrow reaction) and mercury(II) trifluoroacetate (modified Treibs oxidation) have been used previously to effect allylic oxidation on these substrates en route to biologically active compounds. In both these reactions, which involve electrophilic addition to the delta5-bond, the 3-acyloxy substituent plays a significant role. In this report, the effect of introducing other substituents proximate to the delta5-bond has been studied by using derivatives of 3beta-acetoxyandrost-5-en-17-one (1), namely, 3beta,4beta-diacetoxyandrost-5-en-17-one (13), 3beta,19-diacetoxyandrost-5-en-17-one (14), 3beta-acetoxyandrost-5-ene-7,17-dione (15), and 3beta-acetoxy-4,4-dimethylandrost-5-en-17-one (17). Our results indicate that in both sets of reactions the effect of the introduced functional groups was pronounced. In the Petrow reaction, electrophilic addition rather than allylic oxidation on the diacetates was observed. With the Treibs reaction, allylic oxidation on the diacetates occurred. The 7-keto and 4,4-dimethyl steroids proved to be poor substrates in both reactions.

Androstenes↗

PubMed1998

Microbial hydroxylation of acetylaminosteroids.

An investigation of the microbial biotransformation of a range of 3 beta-, 17 beta-, and 20-acetylamino C18 to C21 steroids by microorganisms known to hydroxylate conventional steroids has been undertaken, using Aspergillus ochraceus, Bacillus megaterium, Curvularia lunata, and Rhizoputus arrhizus. A. ochraceus and B. megaterium gave products of 11 alpha- and 15 beta-hydroxylation, respectively. In the case of C. lunata, the products were predominantly those of this organism's normal C-11 beta- and C-14 alpha-hydroxylating pathways, but in one instance, 3 beta-acetylamino-7 alpha-hydroxy-5 alpha-androstan-17-one, appeared to results from direction of the site of hydroxylation by the substitution pattern of the substrate. The products from R. arrhizus generally corresponded to those previously obtained from normal steroids of similar skeleton, with 6 beta- 11 alpha-hydroxylation predominating, but again the sites of hydroxylation and the range of hydroxylated products were found to depend on the substitution pattern of the substrate.

Aspergillus ochraceus↗

PubMed1998

The scope and limitations of the reaction of delta 5-steroids with mercury(II) trifluoroacetate.

The effect of the C-3 substituent on the reaction of androst-5-enes with mercury(II) trifluoroacetate in dichloromethane (modified Treibs oxidation) was investigated. 3 beta-Acyloxyandrost-5-en-17-ones gave 3 beta-acyloxy-6 beta-hydroxyandrost-4-en-17-ones accompanied by 3 beta-acyloxy-6-chloromercuriandrost-5-en-17-ones. 3 beta-Acetoxy-6 beta-trifluoroacetoxyandrost-4-en-17-one and 3 beta-acetoxy-4 beta-trifluoroacetoxyandrost-5-en-17-one were revealed to be intermediates in the reaction. The formation of the chloromercury steroids indicated participation in the reaction by the solvent. With 3 alpha-acetoxyandrost-5-en-17-one as substrate, a complete reversal in the product distribution was observed. 3 beta-Haloandrost-5-en-17-ones gave mainly products that reflected SN1 substitution of the halide. 3 beta-Hydroxy- and 3 beta-trifluoroacetoxyandrost-5-en-17-ones were formed. 3 beta-Methoxyandrost-5-en-17-one afforded in nearly identical yields androst-4-ene-3,17-dione, 3 beta-methoxy-6 beta-hydroxyandrost-4-en-17-one, 3 beta-methoxy-6-chloromercuriandrost-5-en-17-one and 6 beta-hydroxyandrost-4-ene-3,17-dione while androst-5-en-17-one yielded 3 beta,6 beta-dihydroxyandrost-4-en-17-one, androst-5-ene-7,17-dione and androst-4-ene-3,17-dione. The effects of solvent and other mercury salts on the reaction were also studied. Treibs oxidation was successful in chloroform, carbon tetrachloride, and dibromomethane, but not in other solvents tested. 3 beta-Acetoxy-6-bromomercuriandrost-5-en-17-one was obtained in dibromomethane. Replacement of the reagent by mercury(II) trichloroacetate altered the intermediates formed but not the products. Mercury(II) tribromoacetate was unreactive, however.

Androstenes↗