About: Diastereoselective Aziridination of Chiralα-Carbonyl Enoates1

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : Diastereoselective Aziridination of Chiralα-Carbonyl Enoates1 Goto Sponge NotDistinct Permalink

Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_14/w
Subject	Note
Title	Diastereoselective Aziridination of Chiralα-Carbonyl Enoates1
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_14/101021jo025670x/m/web http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_14/101021jo025670x/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_14/101021jo025670x/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_14/101021jo025670x/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_14/101021jo025670x/authorship/4 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_14/101021jo025670x/authorship/1
Author	Fioravanti Stefania Morreale Alberto Tardella Paolo A. Pellacani Lucio
Abstract	Nosyloxycarbamates very efficiently aziridinateoptically active α-carbonyl enoates with high levels ofdiastereoselectivity under mild conditions and in a straightforward process.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata