About: Trimethylsilylethynyl Ketones asSurrogates for Ethynyl Ketones in theDouble Michael Reaction

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_9/w
Subject	Note
Title	Trimethylsilylethynyl Ketones asSurrogates for Ethynyl Ketones in theDouble Michael Reaction
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_9/101021jo0163086/m/print http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_9/101021jo0163086/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_9/101021jo0163086/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_9/101021jo0163086/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_9/101021jo0163086/authorship/1
Author	Holeman Derrick S. Rasne Ravindra M. Grossman Robert B.
Abstract	Trimethylsilylethynyl ketones can be desilylatedin the presence of a tethered carbon diacid and induced toundergo a double Michael reaction in situ. The trimethylsilylethynyl ketones can serve as surrogates of ethynylketones that are difficult to prepare or isolate.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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