In order to investigate the effects of dimethylamino substituent at postion 2 of the dihydropyridine nucleus on its activity, dialkyl 1,4-dihydro-2-[2-(dimethy- lamino) ethyl]-6-methyl-4-(1-benzyl-2-alkylthio-5-imidazolyl)-3,5-pyrdinedicar- boxylates (6a-f) were synthesized. The synthesis was started from dialkyl 1,4- dihydro-2,6-dimethyl-4-(1-benzyl-2-alkylthio-5-imidazolyl)-3,5-pyridine...

In order to investigate the effects of dimethylamino substituent at position 2 of the dihydropyridine nucleus on activity, starting from dialkyl l ,4-dihydro-2,6-dimethyl-4- (l-benzyl-2-alkylthio-5-imidazolyl)-3,5-pyridinedicarboxylates (5a-f) which their synthesis and effects as calcium channel antagonist on guinea-pig ileum has been reported previously, dialkyl l,4-dihydro-2-[2-(dimethyla...

In this study, we have developed an efficient protocol for synthesis of phosphorus-substituted heterocycles through reaction between 2-Aryl quinoxalines and dialkyl phosphites under transition-metal-free conditions. Here, K2S2O8 has been used as the sole oxidant facile phosphorus substituted derivates. A variety heteroaryl phosphonate derivatives synthesized optimized conditions in good to exce...

In the title compound, C(15)H(24)O(2), a natural dialkyl-resorcinol commonly named stemphol, the mol-ecules are linked into C(6) and C(2) (2)(4) chains and R(4) (4)(16) rings by inter-molecular O-H⋯O hydrogen bonds, creating mol-ecular sheets parallel to the (010) plane. The alkyl chains are directed orthogonally away from these planes in almost complete extension.

Regioselective bromine-lithium exchange reactions on polybrominated biaryls enable the modular synthesis of various polysubstituted biphenyls such as bis(dialkylphosphino)-, bis(diarylphosphino)- and dialkyl(diaryl)phosphinobiphenyls. All permutations of substituents at the ortho positions of the biphenyls are possible. In a similar manner, one can gain access to monophosphine analogues. So far...

[reaction: see text] Enamine [2 + 2] cycloadditions can be achieved in useful yields simply by stirring a mixture of an aldehyde, diethylamine, a dialkyl fumarate, and potassium carbonate in acetonitrile at 25 degrees C, conditions that are compatible with the presence of a potential leaving group on the beta-position of the intermediate enamine. Methylation and elimination of the product cyclo...

The Abramov reaction, a base-catalyzed nucleophilic addition of dialkyl H-phosphonates (phosphites) to carbonyl compounds, was performed with oxidized quinine derivatives as the substrates. Homologous aldehydes obtained from the vinyl group reacted in a typical way which led to α-hydroxyphosphonates, first reported compounds containing a direct P-C bond between the quinine carbon skeleton and a...

dialkyl glycerol tetraethers 2 3 Xiao-Lei Liu a, b, *, Daniel Birgel c, Felix J. Elling a, , Paul A. Sutton , Julius S. Lipp , 4 Rong Zhu a, , Chuanlun Zhang , Martin Könneke , Jörn Peckmann c, , Steven J. 5 Rowland , Roger E. Summons , Kai-Uwe Hinrichs a 6 7 8 a Organic Geochemistry Group, MARUM Center for Marine Environmental Sciences and 9 Department of Geosciences, University of Bremen, 283...