|
|
Ïóáëèêàöèè â áàçå äàííûõ Math-Net.Ru
-
Annulation of 1-methylisoquinoline with pyrrolylacetylenic ketones: catalyst-free stereoselective synthesis of (E)-acylethenylpyrrolo[1',2':3,4]imidazo[2,1-a]isoquinolines
Mendeleev Commun., 34:5 (2024), 691–693
-
A straightforward access to 2-hydroxyoxazino[3,2-f ]phenanthridines from phenanthridine, oxalylacetylenes and water
Mendeleev Commun., 32:4 (2022), 439–442
-
Cyanoacetylene-driven base catalyzed synthesis of dihydropyrimidophenanthridinones from phenanthridine and water
Mendeleev Commun., 30:1 (2020), 12–14
-
2-(5-Arylterphenyl-4-yl)quinolines from 2-methylquinoline and 1-(het)aryl-3-phenylprop-2-yn-1-ones in just a one step: A miracle of molecular interplay
Mendeleev Commun., 28:3 (2018), 267–269
-
Ring-opening of pyridines and imidazoles with electron-deficient acetylenes: En route to metal-free organic synthesis
Mendeleev Commun., 27:2 (2017), 109–115
-
Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
Mendeleev Commun., 26:1 (2016), 16–18
-
The reaction of 1,5,6-trimethylbenzimidazole with 1,3-diphenylprop-2-yn-1-one and water: en route to β-amino enones and benzodiazocinones
Mendeleev Commun., 25:4 (2015), 254–256
-
Vinylation of trialkylamines with acyl- and cyanoacetylenes via C–N bond cleavage in the presence of water
Mendeleev Commun., 24:4 (2014), 209–210
-
2,4-Diphenylpyrido[2,1-a]isoquinolinium nitrite from the domino reaction between isoquinoline, 1,3-diphenylprop-2-yn-1-one and nitromethane
Mendeleev Commun., 24:3 (2014), 156–158
-
(Z)-1-Organyl-2-(2,4-dicyano-1,3-diphenyl-1,3-butadienyl)imidazoles from 1-substituted imidazoles with phenylcyanoacetylene
Mendeleev Commun., 19:1 (2009), 42–44
-
A peculiar vinylation of 1-substituted imidazoles with, α,β-acetylenic γ-hydroxyacid nitriles
Mendeleev Commun., 17:4 (2007), 237–238
-
Reaction of anabasine with 3-(1-hydroxycyclohexyl)-2-propynenitrile: a new route to functionalised anabasine alkaloids
Mendeleev Commun., 15:1 (2005), 33–35
© , 2025