About: Sequential Elimination−CyclopropanationReactions Promoted by Samarium: HighlyDiastereoselective Synthesis ofCyclopropylamides

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/w
Subject	Note
Title	Sequential Elimination−CyclopropanationReactions Promoted by Samarium: HighlyDiastereoselective Synthesis ofCyclopropylamides
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/101021jo0262098/m/print http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/101021jo0262098/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/101021jo0262098/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/101021jo0262098/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/101021jo0262098/authorship/3
Author	Concellón José M. Llavona Ricardo Rodríguez-Solla Humberto
Abstract	trans-Cyclopropanamides were obtained, in highyield, from 2-chloro-3-hydroxyamides by a sequenced elimination−cyclopropanation process promoted by Samarium/diiodomethane or Samarium diiodide and Samarium/diiodomethane.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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