Reductive Heck reactions of N-arylamino-substituted tricyclic imides
نویسندگان
چکیده
منابع مشابه
Reductive Heck reactions of N-methyl-substituted tricyclic imides.
The palladium-catalyzed hydroarylation of N-methyl-substituted tricyclic imides was studied in order to find a new stereoselective access to a series of new exo-aryl(hetaryl)-substituted tricyclic N-methylimides.
متن کامل1,3-dipolar cycloaddition reactions of N-methyl-substituted tricyclic imides.
The [3+2] cycloadditions of N-methyl derivatives of unsaturated imides with various nitrile oxides to yield new bridged isoxazoline derivatives with potential biological activity is described.
متن کاملReductive Heck reactions and [3+2] cycloadditions of unsaturated N,N'-bistricyclic imides.
The C-C coupling of N,N'-bis(5-norbornene-2,3-dicarboximide) (3) and N,N'-bis(7-oxa-5-norbornene-2,3-dicarboximide) (6) with aryl and heteroaryl iodides gave under reductive Heck conditions the C-aryl(hetaryl), substituted N,N'-bistricyclic imides 7a-f and 8a,b. The fused spiro-1,3-indandionolylpyrrolidine compounds, 9, 10 and 11 were also obtained from ninhydrine, sarcosine and 3 or 6 via [3+2...
متن کاملSynthesis and biological evaluation of N-substituted polycyclic imides derivatives.
The preparation of 16 derivatives of 3,5,8-trioxo-4-azatricyclo- [5.2.2.0(2.6)]undec-1-yl acetate and 8 derivatives of 1-isobutoxy-4-azatricyclo[5.2.2.0(2.6)]undecane-3,5,8-trione was described. Substituents to the imide N-atom were alkyl-(aryl)piperazine fragments with an alkyl linker being propyl or butyl group. Selected newly obtained compounds were evaluated in vitro against anti-HIV-1 acti...
متن کاملEpibatidine alkaloid chemistry: 5. Domino-Heck reactions of azabicyclic and tricyclic systems.
Palladium-catalyzed hydroarylations and additional domino reactions of aza-bicyclic and tricyclic norbornene derivatives were investigated and a series of new epibatidine analogues were synthesized.
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ژورنال
عنوان ژورنال: Journal of the Serbian Chemical Society
سال: 2016
ISSN: 0352-5139,1820-7421
DOI: 10.2298/jsc160218062a