About: Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles

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About: Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles Goto Sponge NotDistinct Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	skos:Concept http://linked.opendata.cz/ontology/domain/vavai/Vysledek
rdfs:seeAlso	http://www.benthamdirect.org/pages/content.php?COC/2011/00000015/00000024/0003D.SGM
Description	During last decade the field of Organocatalysis emerged as one of the cornerstones of organic asymmetric synthesis. The use of organocatalysis has some advantages such as metal free reactions, environmentally friendly conditions, does not need to use dry solvents or inert atmosphere, avoid the use of protecting groups, etc... For these reasons, several research groups have focused their efforts on the development of new organocatalytic methodologies that render the final products in excellent yields and stereoselectivities. Concretely, the organocatalytic synthesis of 5 and 6 membered heterocycles has attracted much attention. In this review we have the aim to describe the different organocatalytic methodologies developed since in the synthesis of 5 and 6 heterocycles. During last decade the field of Organocatalysis emerged as one of the cornerstones of organic asymmetric synthesis. The use of organocatalysis has some advantages such as metal free reactions, environmentally friendly conditions, does not need to use dry solvents or inert atmosphere, avoid the use of protecting groups, etc... For these reasons, several research groups have focused their efforts on the development of new organocatalytic methodologies that render the final products in excellent yields and stereoselectivities. Concretely, the organocatalytic synthesis of 5 and 6 membered heterocycles has attracted much attention. In this review we have the aim to describe the different organocatalytic methodologies developed since in the synthesis of 5 and 6 heterocycles. (en)
Title	Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles (en)
skos:prefLabel	Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles (en)
skos:notation	RIV/00216208:11310/11:10105200!RIV12-MSM-11310___
http://linked.open...avai/riv/aktivita	Z
http://linked.open...avai/riv/aktivity	Z(MSM0021620857)
http://linked.open...iv/cisloPeriodika	24
http://linked.open...vai/riv/dodaniDat	2012
http://linked.open...aciTvurceVysledku	Veselý, Jan
http://linked.open.../riv/druhVysledku	J - Článek v odborném periodiku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Univerzita Karlova v Praze / Přírodovědecká fakulta
http://linked.open...dnocenehoVysledku	197432
http://linked.open...ai/riv/idVysledku	RIV/00216208:11310/11:10105200
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	cascade reaction; azomethine ylides; conjugate addition; alpha,beta-unsaturated aldehydes; nitroso aldol/michael reaction; asymmetric 1,3-dipolar cycloaddition; michael-aldol reactions; pictet-spengler reactions; one-pot synthesis; Diels-Alder reaction (en)
http://linked.open.../riv/klicoveSlovo	3-dipolar cycloaddition alpha asymmetric 1 azomethine ylides beta-unsaturated aldehydes cascade reaction conjugate addition michael-aldol reactions nitroso aldol/michael reaction one-pot synthesis pictet-spengler reactions Diels-Alder reaction
http://linked.open...odStatuVydavatele	NL - Nizozemsko
http://linked.open...ontrolniKodProRIV	[2F43BC25513E]
http://linked.open...i/riv/nazevZdroje	Current Organic Chemistry
http://linked.open...in/vavai/riv/obor	CC
http://linked.open...ichTvurcuVysledku	1 (xsd:int)
http://linked.open...cetTvurcuVysledku	2 (xsd:int)
http://linked.open...UplatneniVysledku	2011
http://linked.open...v/svazekPeriodika	15
http://linked.open...iv/tvurceVysledku	Veselý, Jan Rios, Ramon
http://linked.open...ain/vavai/riv/wos	000299645800003
http://linked.open...n/vavai/riv/zamer	Nové molekulární systémy pro pokročilé aplikace prospěšné pro zdraví a šetrné k životnímu prostředí
issn	1385-2728
number of pages	37 (xsd:int)
http://localhost/t...ganizacniJednotka	11310

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