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Imino [4+4] cycloaddition products as exclusive and biologically relevant acrolein-amine conjugates are intermediates of 3-formyl-3,4-dehydropiperidine (FDP), an acrolein biomarker
Takamatsu M., Fukase K., Kurbangalieva A., Tanaka K.
of the reaction, through an imino [4+4] cycloaddition, of biologically relevant amines with acrolein
Benzoyl and trichloroacetyl isocyanates in cyclo-formation reactions
Arbuzov B., Zobova N., Balabanova F.
1. Benzoyl isocyanate reacts with acrolein and diphenylacetylene by the 1,2-cyclo-addition type. 2
Reaction of benzoyl and trichloroacetyl isocyanates with cyclic enamines
Arbuzov B., Zobova N., Balabanova F.
, and piperidinocyclopentene on the type of 1,4-cycloaddition, with the formation of 1,3-oxazin-4-one derivatives, while
Sydnone-alkyne cycloaddition: Which factors are responsible for reaction rate ?
Gimadiev T., Klimchuk O., Nugmanov R., Madzhidov T., Varnek A.
. Reconstructed reaction path supported two-step mechanism: cycloaddition followed by retro-Diels-Alder reaction
Cycloaddition of furfurylamines to maleic anhydride and its substituted derivatives
Zaytsev V.P., Mikhailova N.M., Airiyan I.K., Galkina E.V., Golubev V.D., Nikitina E.V., Zubkov F.I., Varlamov A.V.
The regio- and stereoselectivity of the [4+2] cycloaddition of maleic, citraconic, dichloromaleic
New synthetic approach to epoxyisoindolo[2,1-a]quinolines based on cycloaddition reactions of 2-furyl-substituted tetrahydroquinolines with maleic anhydride and acryloyl chloride
Zubkov F.I., Zaitsev V.P., Peregudov A.S., Mikhailova N.M., Varlamov A.V.
through successive acylation at the quinoline nitrogen atom and intramolecular exo-[4+2]-cycloaddition
Tandem dihetero-Diels-Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes
Litvinov I., Efimov S., Musin R., Klochkov V., Mironov V.
and NMR spectroscopy. The process involves dihetero-Diels-Alder and Huisgen 1,3-dipolar cycloaddition
Unusual [3+2]-cycloaddition of acrylic acid derivatives to 7-formyl-4,5,6,7-tetrahydro-4,5,7-trimethylpyrrolo[3,2-c]-pyridine under Michael reaction conditions
Varlamov A.V., Borisova T.N., Barge S.B., Voskresenskii L.G., Chernyshev A.I., Semenova E.M.
8-Substituted tetrahydropyrido[3,2-e]pyrrolizines are formed in the [3+2]-cycloaddition of 2
Lithium and magnesium perchlorate solutions and their influence on the rate and equilibrium of some cycloaddition reactions
Kiselev V.
on some (4+2)-, (3+2)-and (2+2)-cycloaddition reactions have been discussed. Several explanations
High-pressure influence on the rate of diels-alder cycloaddition reactions of maleic anhydride with some dienes
Kiselev V.
and reaction were measured in toluene solution for the Diels-Alder cycloaddition reaction of maleic anhydride

Страница 11 из 36

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