This HTML5 document contains 59 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/
n19http://localhost/temp/predkladatel/
n15http://linked.opendata.cz/resource/domain/vavai/projekt/
n13http://linked.opendata.cz/resource/domain/vavai/riv/tvurce/
n22http://linked.opendata.cz/resource/domain/vavai/subjekt/
n17http://linked.opendata.cz/ontology/domain/vavai/
n21http://linked.opendata.cz/resource/domain/vavai/zamer/
shttp://schema.org/
skoshttp://www.w3.org/2004/02/skos/core#
rdfshttp://www.w3.org/2000/01/rdf-schema#
n3http://linked.opendata.cz/ontology/domain/vavai/riv/
n7http://bibframe.org/vocab/
n2http://linked.opendata.cz/resource/domain/vavai/vysledek/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n10http://linked.opendata.cz/ontology/domain/vavai/riv/klicoveSlovo/
n4http://linked.opendata.cz/ontology/domain/vavai/riv/duvernostUdaju/
xsdhhttp://www.w3.org/2001/XMLSchema#
n18http://linked.opendata.cz/ontology/domain/vavai/riv/jazykVysledku/
n11http://linked.opendata.cz/ontology/domain/vavai/riv/aktivita/
n8http://linked.opendata.cz/ontology/domain/vavai/riv/druhVysledku/
n6http://linked.opendata.cz/ontology/domain/vavai/riv/obor/
n16http://linked.opendata.cz/resource/domain/vavai/vysledek/RIV%2F00216208%3A11310%2F13%3A10159148%21RIV14-MSM-11310___/
n5http://reference.data.gov.uk/id/gregorian-year/

Statements

Subject Item
n2:RIV%2F00216208%3A11310%2F13%3A10159148%21RIV14-MSM-11310___
rdf:type
n17:Vysledek skos:Concept
rdfs:seeAlso
http://dx.doi.org/10.1002/anie.201301739
dcterms:description
A general approach to dibenzo[5]-, dibenzo[6]-, and dibenzo[7]helicenes as well as their functionalized derivatives has been developed. These helically chiral aromatics can be synthesized within four to six operations in overall yields ranging from 24% to 67% by employing a short sequence of reliable processes such as Sonogashira coupling, Suzuki-Miyaura coupling, desilylation, and [2+2+2] alkyne cycloisomerization. A general approach to dibenzo[5]-, dibenzo[6]-, and dibenzo[7]helicenes as well as their functionalized derivatives has been developed. These helically chiral aromatics can be synthesized within four to six operations in overall yields ranging from 24% to 67% by employing a short sequence of reliable processes such as Sonogashira coupling, Suzuki-Miyaura coupling, desilylation, and [2+2+2] alkyne cycloisomerization.
dcterms:title
Rapid Access to Dibenzohelicenes and their Functionalized Derivatives Rapid Access to Dibenzohelicenes and their Functionalized Derivatives
skos:prefLabel
Rapid Access to Dibenzohelicenes and their Functionalized Derivatives Rapid Access to Dibenzohelicenes and their Functionalized Derivatives
skos:notation
RIV/00216208:11310/13:10159148!RIV14-MSM-11310___
n17:predkladatel
n22:orjk%3A11310
n3:aktivita
n11:I n11:P n11:Z
n3:aktivity
I, P(GAP207/10/2207), Z(MSM0021620857)
n3:cisloPeriodika
38
n3:dodaniDat
n5:2014
n3:domaciTvurceVysledku
n13:3157962
n3:druhVysledku
n8:J
n3:duvernostUdaju
n4:S
n3:entitaPredkladatele
n16:predkladatel
n3:idSjednocenehoVysledku
101473
n3:idVysledku
RIV/00216208:11310/13:10159148
n3:jazykVysledku
n18:eng
n3:klicovaSlova
helical structures; chirality; asymmetric synthesis; aromaticity; alkynes; cycloisomerization; enantioselective synthesis; dibenzohelicene
n3:klicoveSlovo
n10:chirality n10:aromaticity n10:dibenzohelicene n10:helical%20structures n10:enantioselective%20synthesis n10:cycloisomerization n10:alkynes n10:asymmetric%20synthesis
n3:kodStatuVydavatele
GB - Spojené království Velké Británie a Severního Irska
n3:kontrolniKodProRIV
[31868E37D64B]
n3:nazevZdroje
Angewandte Chemie - International Edition
n3:obor
n6:CC
n3:pocetDomacichTvurcuVysledku
1
n3:pocetTvurcuVysledku
11
n3:projekt
n15:GAP207%2F10%2F2207
n3:rokUplatneniVysledku
n5:2013
n3:svazekPeriodika
52
n3:tvurceVysledku
Pohl, Radek Cocq, Kevin Stará, Irena G. Vacek Chocholoušová, Jana Bednárová, Lucie Jančařík, Andrej Vacek, Jaroslav Rybáček, Jiří Fiedler, Pavel Císařová, Ivana Starý, Ivo
n3:wos
000324309900020
n3:zamer
n21:MSM0021620857
s:issn
1433-7851
s:numberOfPages
6
n7:doi
10.1002/anie.201301739
n19:organizacniJednotka
11310