Results 121 to 130 of about 17,972 (231)

1, 3-Dipolar Cycloaddition of Nitrones to Enamines

open access: yesNippon kagaku zassi, 1971
Otohiko TSUGE   +2 more
openaire   +2 more sources

Synthesis of Pyrazolidines (5-membered heterocyclic rings) through 1, 3- dipolar cycloadditions of azomethine imines

open access: yesIOSR Journal of Applied Chemistry, 2012
Dipolar cycloadditions of azomethine imines, formed in situ from aldehydes and hydrazines with electron deficient dipolarophiles produced pyrazolidines. Monosubstituted dipolarophiles afford principally 4substituted pyrazolidines.
openaire   +1 more source

Cycloaddition reactions of nitrosoalkenes, azoalkenes and nitrile oxides mediated by hydrotalcite [PDF]

open access: yes, 2012
Mg:Al 3:1 hydrotalcite (Ht), used in catalytic quantities, promotes the generation of nitrosoalkenes, azoalkenes and nitrile oxides. These can be intercepted in situ by heterocycles and olefins in [4+2] and [3+2] cycloaddition reactions, producing ...
Lemos, A., Lourenço, J. P.
core  

Structure, liquid and solid state synthesis for dimers via [3+3] dipolar cycloadditions [PDF]

open access: yesArkivoc, 2005
Gheorghita N. Zbancioc   +3 more
openaire   +1 more source

Synthesis of Some New 3-Pyrrolidinylquinoline Derivatives via 1,3-Dipolar Cycloaddition of Stabilized Azomethine Ylides to Quinolinyl α,β- Unsaturated Ketones

open access: yes, 2010
International audienceN-Metallated azomethine ylide generated from methyl (E)-N-benzylideneglycinate, LiBr and triethylamine underwent cycloaddition to quinolyl α,β- unsaturated ketones with excellent diastereoselectivity to afford new functionalised 3 ...
Belfaitah, Ali   +5 more
core   +1 more source

Structure-Activity Relationships for 1,3-Dipolar Cycloaddition Reactions of Criegee Intermediates with Carbonyls. [PDF]

open access: yesACS Earth Space Chem
Cornwell ZA   +4 more
europepmc   +1 more source

Nitrone chemistry: a versatile gateway to diverse heterocycles. [PDF]

open access: yesRSC Adv
Mohapatra S   +4 more
europepmc   +1 more source

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