Enantiopure 2-aryl-2-methyl cyclopentanones by an asymmetric chelation-controlled Heck reaction using aryl bromides: increased preparative scope and effect of ring size on reactivity and selectivity

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Title
Enantiopure 2-aryl-2-methyl cyclopentanones by an asymmetric chelation-controlled Heck reaction using aryl bromides: increased preparative scope and effect of ring size on reactivity and selectivity
Authors
Keywords
-
Journal
TETRAHEDRON-ASYMMETRY
Volume 19, Issue 9, Pages 1120-1126
Publisher
Elsevier BV
Online
2008-05-20
DOI
10.1016/j.tetasy.2008.04.004

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