This HTML5 document contains 37 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
dctermshttp://purl.org/dc/terms/
n17http://localhost/temp/predkladatel/
n10http://linked.opendata.cz/resource/domain/vavai/projekt/
n4http://linked.opendata.cz/resource/domain/vavai/riv/tvurce/
n14http://linked.opendata.cz/resource/domain/vavai/vysledek/RIV%2F00216224%3A14310%2F07%3A00020844%21RIV11-GA0-14310___/
n12http://linked.opendata.cz/ontology/domain/vavai/
n18http://linked.opendata.cz/resource/domain/vavai/zamer/
skoshttp://www.w3.org/2004/02/skos/core#
n3http://linked.opendata.cz/ontology/domain/vavai/riv/
n2http://linked.opendata.cz/resource/domain/vavai/vysledek/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n9http://linked.opendata.cz/ontology/domain/vavai/riv/klicoveSlovo/
n15http://linked.opendata.cz/ontology/domain/vavai/riv/duvernostUdaju/
xsdhhttp://www.w3.org/2001/XMLSchema#
n16http://linked.opendata.cz/ontology/domain/vavai/riv/jazykVysledku/
n8http://linked.opendata.cz/ontology/domain/vavai/riv/aktivita/
n13http://linked.opendata.cz/ontology/domain/vavai/riv/druhVysledku/
n11http://linked.opendata.cz/ontology/domain/vavai/riv/obor/
n6http://reference.data.gov.uk/id/gregorian-year/

Statements

Subject Item
n2:RIV%2F00216224%3A14310%2F07%3A00020844%21RIV11-GA0-14310___
rdf:type
skos:Concept n12:Vysledek
dcterms:description
alpha-Substituted o-alkylphenacyl derivatives were found to undergo photoinduced selective formation of the products in excellent chemical and moderate quantum yields. The reaction mechanism, studied by laser flash photolysis, was found to be largely dependent on the reaction conditions and the structure of the starting material. This procedure is suggested to be a facile synthetic route to some target skeletons, such as indanone, isobenzofuran, or methyleneindenone derivatives. alpha-Substituted o-alkylphenacyl derivatives were found to undergo photoinduced selective formation of the products in excellent chemical and moderate quantum yields. The reaction mechanism, studied by laser flash photolysis, was found to be largely dependent on the reaction conditions and the structure of the starting material. This procedure is suggested to be a facile synthetic route to some target skeletons, such as indanone, isobenzofuran, or methyleneindenone derivatives.
dcterms:title
The Photoenolization Reaction: Synthetic and Mechanistic Variations The Photoenolization Reaction: Synthetic and Mechanistic Variations
skos:prefLabel
The Photoenolization Reaction: Synthetic and Mechanistic Variations The Photoenolization Reaction: Synthetic and Mechanistic Variations
skos:notation
RIV/00216224:14310/07:00020844!RIV11-GA0-14310___
n3:aktivita
n8:P n8:Z
n3:aktivity
P(GA203/05/0641), Z(MSM0021622413)
n3:dodaniDat
n6:2011
n3:domaciTvurceVysledku
n4:9308695 n4:1626418 Tazhe Veetil, Aneesh
n3:druhVysledku
n13:O
n3:duvernostUdaju
n15:S
n3:entitaPredkladatele
n14:predkladatel
n3:idSjednocenehoVysledku
441252
n3:idVysledku
RIV/00216224:14310/07:00020844
n3:jazykVysledku
n16:eng
n3:klicovaSlova
Photochemistry; photoenolization
n3:klicoveSlovo
n9:Photochemistry n9:photoenolization
n3:kontrolniKodProRIV
[1D7D0936BA27]
n3:obor
n11:CC
n3:pocetDomacichTvurcuVysledku
3
n3:pocetTvurcuVysledku
4
n3:projekt
n10:GA203%2F05%2F0641
n3:rokUplatneniVysledku
n6:2007
n3:tvurceVysledku
Plíštil, Lukáš Literák, Jaromír Tazhe Veetil, Aneesh Klán, Petr
n3:zamer
n18:MSM0021622413
n17:organizacniJednotka
14310