| Attributes | Values |
|---|
| rdf:type
| |
| description
| - videnskabelig artikel (da)
- article científic (ca)
- articolo scientifico (it)
- artigo científico (pt)
- bilimsel makale (tr)
- vedecký článok (sk)
- vetenskaplig artikel (sv)
- vědecký článek (cs)
- wetenschappelijk artikel (nl)
- wissenschaftlicher Artikel (de)
- научни чланак (sr)
- article scientifique (fr)
- artículu científicu espublizáu en 2010 (ast)
- наукова стаття, опублікована у квітні 2010 (uk)
- scientific article published on 13 April 2010 (en)
- مقالة علمية نشرت في 13 أبريل 2010 (ar)
|
| publication date
| |
| publication date
| |
| language of work or name
| |
| language of work or name
| |
| cites work
| |
| cites work
| - Total Synthesis of (±)-Lysergic Acid, Lysergol, and Isolysergol by Palladium-Catalyzed Domino Cyclization of Amino Allenes Bearing a Bromoindolyl Group
- Regio- and diastereoselective insertion of allenes into stable oxapalladacycles with a metal-bonded stereogenic carbon. preparation of contiguously substituted 3,4-dihydro-2H-1-benzopyrans
- Phosphine-free palladium-catalyzed allene carbopalladation/allylic alkylation domino sequence: a new route to 4-(alpha-styryl) gamma-lactams.
- Pd-catalyzed regio- and stereoselective cyclization-heck reaction of monoesters of 1,2-allenyl phosphonic acids with alkenes.
- A new method for the generation of indole-2,3-quinodimethanes and 2-(N-alkoxycarbonylamino)-1,3-dienes. Intramolecular Heck/Diels–Alder cycloaddition cascade starting from acyclic α-phosphono enecarbamates
- Palladium-Catalyzed Heck Reaction on 1-Alkoxy-1,3-dienes: A Regioselective γ-Arylation of α,β-Unsaturated Carbonyl Compounds
- Palladium-Catalyzed Domino Carbopalladation/5-exo-Allylic Amination of α-Amino Allenamides: An Efficient Entry to Enantiopure Imidazolidinones
- Synthesis of Medium-Ring Nitrogen Heterocycles via Palladium-Catalyzed Heteroannulation of 1,2-Dienes
- Palladium-catalyzed coupling of allenylphosphonates, phenylallenes, and allenyl esters: remarkable salt effect and routes to novel benzofurans and isocoumarins
- Highly regioselective palladium-catalyzed annulation reactions of heteroatom-substituted allenes for synthesis of condensed heterocycles
- Observation of the first Heck-type cross-coupling reaction of allenes with aryl halides. Synthesis of polysubstituted 1,2-allenyl sulfones
- Polymer-supported palladacycles: efficient reagents for synthesis of benzopyrans with palladium recovery. Relationship among resin loading, Pd:P ratio, and reactivity of immobilized palladacycles
|
| author name string
| |
| author name string
| - Annamaria Deagostino
- Paolo Venturello
- Cristina Prandi
- Silvia Tabasso
|
| rdfs:label
| - The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (en)
- The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (nl)
- The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (ast)
|
| skos:prefLabel
| - The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (en)
- The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (nl)
- The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (ast)
|
| name
| - The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (en)
- The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (nl)
- The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (ast)
|
| title
| |
| title
| - The Heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity (en)
|
| page(s)
| |
| page(s)
| |
| instance of
| |
| instance of
| |
| main subject
| |
| main subject
| |
| PubMed ID
| |
| PubMed ID
| |
| PubMed ID
| |
| published in
| |
| published in
| |
| issue
| |
| volume
| |
| issue
| |
| volume
| |
| DOI
| |
| DOI
| |
| DOI
| - 10.3390/MOLECULES15042667
|
| copyright license
| |
| copyright status
| |
| copyright license
| |
| copyright status
| |
| ResearchGate publication ID
| |
| ResearchGate publication ID
| |
| PMCID
| |
| PMCID
| |
| is about
of | |
| is cites work
of | |
![[RDF Data]](/fct/images/sw-rdf-blue.png)
![[cxml]](/fct/images/cxml_doc.png)
![[csv]](/fct/images/csv_doc.png)
![[text]](/fct/images/ntriples_doc.png)
![[turtle]](/fct/images/n3turtle_doc.png)
![[ld+json]](/fct/images/jsonld_doc.png)
![[rdf+json]](/fct/images/json_doc.png)
![[rdf+xml]](/fct/images/xml_doc.png)
![[atom+xml]](/fct/images/atom_doc.png)
![[html]](/fct/images/html_doc.png)