Synthesis of 5-alkyl-3H-thiolen-2-ones and 5-alkyl-3H-furan-2-ones and condensation reactions at the heterocyclic methylene group

1987 ◽  
Vol 23 (4) ◽  
pp. 377-380 ◽  
Author(s):  
V. A. Sedavkina ◽  
N. A. Morozova ◽  
A. Yu. Egorova ◽  
I. G. Ostroumov
1987 ◽  
Vol 23 (9) ◽  
pp. 951-953
Author(s):  
G. V. Bespalova ◽  
V. A. Sedavkina ◽  
V. G. Kharchenko ◽  
A. D. Shebaldova ◽  
V. I. Labunskaya

ChemInform ◽  
1988 ◽  
Vol 19 (15) ◽  
Author(s):  
G. V. BESPALOVA ◽  
V. A. SEDAVKINA ◽  
V. G. KHARCHENKO ◽  
A. D. SHEBALDOVA ◽  
V. I. LABUNSKAYA

ChemInform ◽  
2007 ◽  
Vol 38 (17) ◽  
Author(s):  
M. A. Sibiryakova ◽  
G. F. Muzychenko ◽  
T. P. Kosulina ◽  
K. S. Pushkareva

2006 ◽  
Vol 42 (7) ◽  
pp. 875-881 ◽  
Author(s):  
M. A. Sibiryakova ◽  
G. F. Muzychenko ◽  
T. P. Kosulina ◽  
K. S. Pushkareva

1995 ◽  
Vol 60 (4) ◽  
pp. 605-611 ◽  
Author(s):  
Pavel Bobáľ ◽  
Roman Gažo ◽  
Rudolf Kada ◽  
Dušan Ilavský ◽  
Naďa Prónayová ◽  
...  

Condensation reactions of 1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinecarbaldehyde with nine acid derivatives containing an active methylene group are described. The obtained products were characterized by their IR, UV, 1H NMR, 13C NMR and mass spectra. The stereochemistry of selected products was studied by 1H and 13C NMR spectroscopy.


2018 ◽  
Vol 22 (6) ◽  
pp. 519-532 ◽  
Author(s):  
Lucas Lima Zanin ◽  
David Esteban Quintero Jimenez ◽  
Luis Pina Fonseca ◽  
Andre Luiz Meleiro Porto

1980 ◽  
Vol 45 (9) ◽  
pp. 2425-2432
Author(s):  
Jiří Krechl ◽  
Josef Kuthan

It has been demonstrated that the EHT method predicts an almost plane form of the heterocyclic ring in 1-methyl-1,4-dihydronicotinamide I (R = CH3) and also reflects satisfactorily character of the covalent bonds in the 4-methylene group. An attempt has been made of calculation of the reaction profile of elimination of the centre 4', and electronic mechanism of its splitting off is discussed.


2001 ◽  
Vol 66 (7) ◽  
pp. 1062-1077 ◽  
Author(s):  
Maarten J. Bakker ◽  
Tapani A. Pakkanen ◽  
František Hartl

Electrochemical properties of tetrahedral clusters [H2Ru2Rh2(CO)12], [HRuRh3(CO)12] and [Rh4(CO)12] were investigated in order to evaluate the influence of metal core composition in the series [H4-xRu4-xRhx(CO)12] (x = 0-4). The cluster [H3Ru3Rh(CO)12] was not available in sufficient quantities. As reported for [H4Ru4(CO)12], electrochemical reduction of the hydride-containing clusters [H2Ru2Rh2(CO)12] and [HRuRh3(CO)12] also results in (stepwise) loss of hydrogen, producing the anions [HRu2Rh2(CO)12]-, [Ru2Rh2(CO)12]2- and [RuRh3(CO)12]-. These anions can also be prepared from the neutral parent clusters via chemical routes. Electrochemical reduction of [Rh4(CO)12] does not result in the formation of any stable tetranuclear anion. Instead, [Rh5(CO)15]- and [Rh6(CO)15]2- are the major reduction products detected in the course of IR spectroelectrochemical experiments. Most likely, these cluster species are formed from the secondary CO-loss product [Rh4(CO)11]2- by fast redox condensation reactions. Their reoxidation regenerates parent [Rh4(CO)12], together with some [Rh6(CO)16]. Unlike [H4Ru4(CO)12] that undergoes photochemical CO-dissociation, [H2Ru2Rh2(CO)12] and [Rh4(CO)12] are completely photostable in neat hexane and dichloromethane as well as in the presence of oct-1-ene.


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