About: CuBr/rac-BINOL-Catalyzed N-Arylations ofAliphatic Amines at Room Temperature

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_2/w
Subject	Note
Title	CuBr/rac-BINOL-Catalyzed N-Arylations ofAliphatic Amines at Room Temperature
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_2/101021jo062060e/m/web http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_2/101021jo062060e/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_2/101021jo062060e/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_2/101021jo062060e/authorship/4 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_2/101021jo062060e/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_2/101021jo062060e/authorship/2
Author	Fu Hua Zhao Yufen Jiang Deshou Jiang Yuyang
Abstract	We have developed an efficient and readily available catalystsystem CuBr/racemic BINOL (1,1‘-binaphthyl-2,2‘-diol) thatcatalyzes N-arylation of aliphatic amines at room temperature, and this inexpensive catalyst system is of high selectivity and tolerance toward various functional groups in thesubstrates.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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