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Intramolecular cyclization of 3β-acetoxy-16-picolinylidene-5-androsten-17-one by catalytic hydrogenation
(Elsevier, 1970)
Intramolecular cyclization by catalytic hydrogenation of 3β-acetoxy-16-picolinylidene-5-androsten-17-one (IV) (80° and 50-60 atm of hydrogen pressure over Pd/C as catalyst) gives rise to the formation of two cyclic products, ...
Ferrous ion induced decomposition of alkyl hypochlorites
(Elsevier, 1981)
The decomposition of primary, secondary and tertiary alkyl hypochlorites induced by ferrous and other one-electron oxidizable metal ions leads to δ-chloro alcohols in yields of 34-76%. In decomposition of tertiary alkyl ...
Lead tetraacetate oxidation of saturated aliphatic alcohols.-III. Unbranched primary and secondary alcohols
(Elsevier, 1965)
The action of lead tetraacetate, in benzene solution, on various unbranched primary and secondary aliphatic alcohols containing 4 to 12 carbon atoms has been investigated and the ratio of carbonyl compounds, cyclic ethers ...
Lead tetra-acetate oxidation of saturated aliphatic alcohols-V. Factors influencing the formation of cyclic ethers and carbonyl compounds
(Elsevier, 1966)
Factors influencing the relative rates of the homolytic and heterolytic processes in the lead tetra-acetate oxidation of unbranched primary and secondary aliphatic alcohols have been investigated, with a view to determine ...
The conformational equilibrium of 1,3-dichloro-5-methylcyclohexane
(Elsevier, 1981)
Two of the stereoisomers of the title compound were prepared and their dipole moments were measured. For the r-1,c-3-dichloro-t-5-methylcyclohexane, the free energy difference between conformers with axial-axial (aa) and ...
Remote functionalisation by ferrous ion-cupric ion induced decomposition of alkyl hydroperoxides
(Pergamon Press, 1979)
By decomposition of alkyl hydroperoxides 1-8 with ferrous sulfate-cupric acetate reagent, intramolecular functionalisation of remote non-activated C atom takes place and unsaturated alcohols with double bond mainly at ...
endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines
(Oxford : Pergamon-Elsevier Science Ltd, 2011)
endo-Mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined as a route to the synthesis of condensed thiazolidines. The scope of these reactions and stereochemical ...
Acid-catalyzed rearrangement of some steroidal isoxazolidines
(Elsevier, 1999)
Acid-catalyzed reaction of the steroidal Δ 1 -unsaturated 3β,5β- epoxyimino compound 2 and Δ 3 -unsaturated 1β,5β-epoxyimino products 3 and 7, results in intramolecular rearrangement involving the N-CH 3 group to give the ...
A novel procedure for the aromatization of ring a in 19-nortestosterone
(Elsevier, 1977)
A convenient, 40% overall yield synthesis of 2,3,17β-triacetoxy-1,3,5(10)-estratriene is described, which involves epoxidation of 19-nortestosterone and subsequent acetylation, lead tetra-acetate acetoxylation of the ...
pi-Annulation reactions of 4-thiazolidinone enaminones in the synthesis of fused bi- and tri-cyclic compounds
(Oxford : Pergamon-Elsevier Science Ltd, 2012)
The a-C position in 4-oxo thiazolidinones functions as one of the three possible nucleophilic sites in these molecules. We used the inherent reactivity of alpha-C of the exocyclic double bond (a so called push pull system) ...