About: Enantio- and Regioselective Heck-Type Reaction of ArylboronicAcids with 2,3-Dihydrofuran

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_10/w
Subject	Article
Title	Enantio- and Regioselective Heck-Type Reaction of ArylboronicAcids with 2,3-Dihydrofuran
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_10/101021jo070170v/m/print http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_10/101021jo070170v/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_10/101021jo070170v/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_10/101021jo070170v/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_10/101021jo070170v/authorship/2
Author	Gelman Dmitri Penn Liza Shpruhman Alina
Abstract	Reported herein is a protocol for the enantioselective Pd(II)-catalyzed Heck-type reaction betweenarylboronic acids and 2,3-dihydrofuran. The highest chemical and optical yields were obtained when aPd(OAc)2/(R)-MeO(biphenylphosphine) or a Pd(OAc)2/(R)-(2,2‘-bis(diphenylphosphino)-1,1‘-binaphthyl)catalyst and a Cu(OAc)2 reoxidant were employed.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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