Results 71 to 80 of about 1,229 (176)
Simple Conversion of Enamines to 2H-Azirines and Their Rearrangements under Thermal Conditions
A variety of substituted enamine derivatives were first found to be conveniently converted to the corresponding 2H-azirines mediated by phenyliodine (III) diacetate (PIDA).
Yunfei Du (1490683) +5 more
core +3 more sources
The reaction of α-azidochalcones with carboxylic acids has been investigated resulting in the formation of α-amido-1,3-diketones under microwave irradiation via in situ formation of 2H-azirine intermediates.
Kandasamy Rajaguru +4 more
doaj +1 more source
A ruthenium-catalyzed intermolecular [3 + 2] cycloaddition of 2H-azirines and activated alkynes is reported, which provides polysubstituted pyrroles in moderate to good yields.
Wan, Boshun +4 more
core +1 more source
Lewis Acid Mediated Alkylation and Diels-Alder Reactions of 2H-Azirines
This thesis describes the use of 2H-azirines as reactivesubstrates in Lewis acid catalysed nucleophilic additions andin the Diels-Alder reaction.A number of carbon nucleophiles have been added to aseries of 2H-azirines in the presence and absence ofBF3 ...
Risberg, Erik
core +2 more sources
Synthesis of Azirinylammonium Salts via Alkylation of DABCO with 2-Halo-2H-azirines
Tertiary (2H-azirin-2-yl)ammonium salts were prepared from methyl 2-halo-3-aryl-2H-azirine-2-carboxylates and 1,4-diazabicyclo[2.2.2]octane in very good to excellent yields. Both iodide and bromide salts are stable enough in crystalline form to be stored
Maksim A. Valiarovskii +3 more
doaj +1 more source
A Review on the Photochemistry of 2H-Azirines [PDF]
Gilgen, Paul +3 more
openaire +2 more sources
A Pd-catalyzed ring-opening reaction of 2H-azirines with carboxylic acids was developed. This reaction undergoes nucleophilic addition between 2,3-diaryl-2H-azirines and carboxylic acids followed by C–N single-bond cleavage and a subsequent thermal ...
Xiao-Ju Si (6287384) +6 more
core +1 more source
TANIGUCHI, Hiroshi, ISOMURA, Kazuaki
openaire +2 more sources
Selective Synthesis of N-Unsubstituted and N-Arylindoles by the Reaction of Arynes with Azirines
The transition-metal-free and temperature-dependent highly selective reaction of arynes with 2H-azirines allowing the synthesis of either N-unsubstituted or N-arylindoles has been developed.
Thangaraj, Manikandan +4 more
core +1 more source
Copper-Catalyzed Highly Enantioselective Addition of a Silicon Nucleophile to 3-Substituted 2H-Azirines Using an Si-B Reagent. [PDF]
Zhao ZY, Cui M, Irran E, Oestreich M.
europepmc +1 more source

