About: Intramolecular 1,3-Dipolar Cycloadditions ofNorbornadiene-Tethered Nitrones

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : Intramolecular 1,3-Dipolar Cycloadditions ofNorbornadiene-Tethered Nitrones Goto Sponge NotDistinct Permalink

Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_15/w
Subject	Article
Title	Intramolecular 1,3-Dipolar Cycloadditions ofNorbornadiene-Tethered Nitrones
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_15/101021jo015610b/m/web http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_15/101021jo015610b/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_15/101021jo015610b/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_15/101021jo015610b/authorship/2
Author	Tranmer Geoffrey K. Tam William
Abstract	Efficient routes to the synthesis of norbornadiene-tethered nitrones have been developed, and theirintramolecular 1,3-dipolar cycloadditions were studied. The cycloadditions occurred in moderateto good yields for a variety of substrates and were found to be highly regio- and stereoselective,giving single regio- and stereoisomers in most cases.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata