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Statements

Subject Item
n2:RIV%2F00216208%3A11310%2F09%3A10000619%21RIV10-GA0-11310___
rdf:type
skos:Concept n17:Vysledek
dcterms:description
An organocatalytic highly enantioselective aza-Baylis-Hillman reaction of alpha,beta-unsaturated aldehydes with in situ generated N-Boc- and N-Cbz-imines is presented. This novel process opens the pathway for the synthesis of beta-amino carbonyl compounds bearing an alpha-alkylidene group under mild and simple conditions. An organocatalytic highly enantioselective aza-Baylis-Hillman reaction of alpha,beta-unsaturated aldehydes with in situ generated N-Boc- and N-Cbz-imines is presented. This novel process opens the pathway for the synthesis of beta-amino carbonyl compounds bearing an alpha-alkylidene group under mild and simple conditions.
dcterms:title
Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines
skos:prefLabel
Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines
skos:notation
RIV/00216208:11310/09:10000619!RIV10-GA0-11310___
n3:aktivita
n19:P n19:Z
n3:aktivity
P(GP203/09/P193), Z(MSM0021620857)
n3:cisloPeriodika
36
n3:dodaniDat
n12:2010
n3:domaciTvurceVysledku
n13:7379153 n13:8465754 n13:5534305 n13:3157962
n3:druhVysledku
n18:J
n3:duvernostUdaju
n7:S
n3:entitaPredkladatele
n6:predkladatel
n3:idSjednocenehoVysledku
317154
n3:idVysledku
RIV/00216208:11310/09:10000619
n3:jazykVysledku
n14:eng
n3:klicovaSlova
Enantioselective; Aza-Baylis-Hillman-Type Reaction; alpha,beta-Unsaturated Aldehydes; N-Boc- and N-Cbz-Imines
n3:klicoveSlovo
n8:beta-Unsaturated%20Aldehydes n8:N-Boc-%20and%20N-Cbz-Imines n8:alpha n8:Aza-Baylis-Hillman-Type%20Reaction n8:Enantioselective
n3:kodStatuVydavatele
DE - Spolková republika Německo
n3:kontrolniKodProRIV
[48CEF93D2D9A]
n3:nazevZdroje
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
n3:obor
n4:CC
n3:pocetDomacichTvurcuVysledku
4
n3:pocetTvurcuVysledku
4
n3:projekt
n9:GP203%2F09%2FP193
n3:rokUplatneniVysledku
n12:2009
n3:svazekPeriodika
Neuveden
n3:tvurceVysledku
Číhalová, Sylva Veselý, Jan Remeš, Marek Císařová, Ivana
n3:wos
000273187700002
n3:zamer
n16:MSM0021620857
s:issn
1434-193X
s:numberOfPages
4
n15:organizacniJednotka
11310