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000841836 1001_ $$0P:(DE-Juel1)157926$$aWorgull, Dennis$$b0$$eCorresponding author$$ufzj
000841836 245__ $$aEnantioselective Synthesis of 2,3-Dihydrofurans via Ammonium Ylides
000841836 260__ $$aWeinheim$$bWiley-VCH Verl.$$c2017
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000841836 520__ $$aA chiral, ammonium ylide based access to tetrasubstituted 2,3-dihydrofurans starting from readily available benzylidene dicarbonyls and bromo acetophenones has been developed. The products are obtained in moderate to good yields with excellent diasteroselectivity and good to excellent enantioselectivity (up to 99:1 e.r.). The employed chiral amine can be recovered in near quantitative yield. The transformation can be run as a three-component one-pot reaction, generating the ammonium salt and ylide in situ. The scope of this reaction includes 17 new dihydrofurans with aromatic or heteroaromatic substituents.
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000841836 7001_ $$0P:(DE-Juel1)168186$$aÖhler, Laura$$b1$$ufzj
000841836 7001_ $$0P:(DE-Juel1)156108$$aStrache, Joss Pepe$$b2
000841836 7001_ $$0P:(DE-HGF)0$$aFriedrichs, Teresa$$b3
000841836 7001_ $$0P:(DE-Juel1)171936$$aUllrich, Patrick$$b4$$ufzj
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