About: New Approach to the Synthesis of MacrocyclicTetralactones via Ring-Closing Metathesis UsingGrubbs' First-Generation Catalyst

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_4/w
Subject	Note
Title	New Approach to the Synthesis of MacrocyclicTetralactones via Ring-Closing Metathesis UsingGrubbs' First-Generation Catalyst
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_4/101021jo062043p/m/print http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_4/101021jo062043p/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_4/101021jo062043p/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_4/101021jo062043p/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_4/101021jo062043p/authorship/3
Author	Muthusamy S. Suresh E. Gnanaprakasam Boopathy
Abstract	A facile and efficient route to synthesize macrocyclictetralactones with different ring sizes having a wide varietyof spacers is described. The application of ring-closingmetathesis for the synthesis of macrocyclic tetralactones isdemonstrated with many examples in excellent yield. Therepresentative structure of macrocyclic tetralactones ischaracterized by X-ray crystallography.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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