Mukaiyama-Michael reactions with α-substituted acroleins - a useful tool for the synthesis of the pectenotoxins and other natural product targets

Kemppainen, Eeva K.

dc.contributor.author	Kemppainen, Eeva K.
dc.date.accessioned	2013-09-16T07:47:21Z
dc.date.available	2013-09-16T07:47:21Z
dc.date.issued	2013
dc.identifier.isbn	978-951-39-5369-0
dc.identifier.other	oai:jykdok.linneanet.fi:1279849
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/42163
dc.format.extent	1 verkkoaineisto (201 sivua)
dc.language.iso	eng
dc.publisher	University of Jyväskylä
dc.relation.ispartofseries	Research report / Department of Chemistry, University of Jyväskylä
dc.rights	In Copyright
dc.subject.other	pektenotoksiini
dc.subject.other	pectenotoxin
dc.subject.other	total synthesis
dc.subject.other	Mukaiyama-Michael reaction
dc.subject.other	organocatalysis
dc.subject.other	2,5-diphenylpyrrolidine
dc.title	Mukaiyama-Michael reactions with α-substituted acroleins - a useful tool for the synthesis of the pectenotoxins and other natural product targets
dc.type	Diss.
dc.identifier.urn	URN:ISBN:978-951-39-5369-0
dc.type.dcmitype	Text	en
dc.type.ontasot	Väitöskirja	fi
dc.type.ontasot	Doctoral dissertation	en
dc.contributor.tiedekunta	Matemaattis-luonnontieteellinen tiedekunta	fi
dc.contributor.tiedekunta	Faculty of Mathematics and Science	en
dc.contributor.laitos	Kemian laitos	fi
dc.contributor.yliopisto	University of Jyväskylä	en
dc.contributor.yliopisto	Jyväskylän yliopisto	fi
dc.contributor.oppiaine	Orgaaninen kemia	fi
dc.relation.issn	0357-346X
dc.relation.numberinseries	no. 172
dc.rights.accesslevel	openAccess
dc.subject.yso	luonnonaineet
dc.subject.yso	myrkylliset aineet
dc.subject.yso	reaktiomekanismit
dc.rights.url	https://rightsstatements.org/page/InC/1.0/

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Mukaiyama-Michael reactions with α-substituted acroleins - a useful tool for the synthesis of the pectenotoxins and other natural product targets

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Toxicological and bioactivity evaluation of blackcurrant press cake, sea buckthorn leaves and bark from Scots pine and Norway spruce extracts under a green integrated approach ﻿

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Stereoselective Synthesis of Spiro-Decalin Oxindole Derivatives via Sequential Organocatalytic Michael-Domino Michael/Aldol Reaction ﻿

Asymmetric Synthesis of Spirocyclic β‐Lactams via Copper‐Catalyzed Kinugasa/Michael Domino Reactions ﻿

Stereocontrol in Diphenylprolinol Silyl Ether Catalyzed Michael Additions : Steric Shielding or Curtin-Hammett Scenario? ﻿

Toxicological and bioactivity evaluation of blackcurrant press cake, sea buckthorn leaves and bark from Scots pine and Norway spruce extracts under a green integrated approach

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Stereoselective Synthesis of Spiro-Decalin Oxindole Derivatives via Sequential Organocatalytic Michael-Domino Michael/Aldol Reaction

Asymmetric Synthesis of Spirocyclic β‐Lactams via Copper‐Catalyzed Kinugasa/Michael Domino Reactions

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