Epalons: Synthesis of New 16α-Carboxymethyl Derivatives

1999 ◽  
Vol 64 (9) ◽  
pp. 1479-1484 ◽  
Author(s):  
Barbora Slavíková ◽  
Alexander Kasal

The title compounds (16α-carboxymethyl-3α-hydroxy-5α-pregnan-20-one and its sodium and triethylammonium salts) were prepared from 20-oxopregna-5,16-dien-3β-yl acetate by conjugate addition of dimethyl malonate and decarboxylation. Inversion of configuration at carbon C-3 was carried out by Mitsunobu acylation with diethyl azodicarboxylate and formic acid in the presence of triphenylphosphine.

1981 ◽  
Vol 34 (9) ◽  
pp. 1913 ◽  
Author(s):  
LN Mander ◽  
GJ Potter ◽  
SG Pyne ◽  
M Woolias

Methyl 3-(6'-oxo-4'-methoxy-5',6',7',8'-tetrahydronaphthalen-1'-yl)propanoate (11) was converted by conventional methods into diazoketone (17) which underwent acid-promoted cyclization to dienone (18). Refunctionalization gave dienone (20) which was subjected to a tandem alkylation, conjugate addition process with the sodium enolate of dimethyl malonate to furnish a 2: 1 mixture of dimethyl (2RS,8aSR,10aSR)-2-methoxymethyloxy-10,12-dioxo-2,3,4,5,6,7,8a,9,10-decahydro-1 H-2,10a-ethano- phenanthrene-8,8-dicarboxylate (21) and its 8a-epimer, respectively. Subsequent manipulations led to lactone (26), but attempts to convert this compound into a gibbane derivative were unsuccessful.


2019 ◽  
Vol 6 (3) ◽  
pp. 104-107
Author(s):  
Marina Vladimirovna Lebedeva ◽  
Alexey Petrovich Antropov ◽  
Alexander Victorovich Ragutkin ◽  
Nicolay Andreevich Yashtulov

In paper electrode materials with palladium nanoparticles on polymer matrix substrates for energy sources have been formed. Nanocomposites were investigated by atomic force and scanning electron microscopy. The catalytic activity of formed electrodes in the formic acid oxidation reaction was evaluated by voltammetry method.


Author(s):  
Manuel Goubet ◽  
Robert Georges ◽  
P. Roy ◽  
Atef Jabri ◽  
Pascale Soulard ◽  
...  

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