About: An Efficient Synthesis of Novel CarbocyclicNucleosides with Use of Ring-ClosingMetathesis from d-Lactose

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_19/w
Subject	Note
Title	An Efficient Synthesis of Novel CarbocyclicNucleosides with Use of Ring-ClosingMetathesis from d-Lactose
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_19/101021jo0202536/m/print http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_19/101021jo0202536/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_19/101021jo0202536/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_19/101021jo0202536/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_19/101021jo0202536/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_19/101021jo0202536/authorship/4
Author	Ro Bong Oh Hong Joon Hee Shim Myung Jung Ko Ok Hyun
Abstract	This paper describes an efficient synthetic routefor various types of novel carbocyclic nucleosides. Therequired stereochemistry of the targeted nucleosides wassuccessfully obtained with use of Grubbs cyclization andTrost allylic alkylation from the carbohydrate chiral template “d-lactose”.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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