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      Recent advances and new concepts for the synthesis of axially stereoenriched biaryls.

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          Abstract

          Axial chirality is a key feature of many important organic molecules, such as biologically active compounds, stereogenic ligands and optically pure materials. Significant efforts in the field of the atropisomeric synthesis of biaryls have hence been undertaken over the past decade. Several major improvements of the already known methods to build up such chiral backbones (e.g. oxidative couplings and stereoselective Suzuki-Miyaura arylations) have been achieved and, in parallel, novel concepts have emerged enabling unprecedented synthetic routes toward molecules of this kind. These outstanding steps further unlocked the door to the preparation of previously difficult-to-access precursors of privileged ligands like BINOL, BINAM, QUINAP and many other molecules of interest.

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          Author and article information

          Journal
          Chem Soc Rev
          Chemical Society reviews
          Royal Society of Chemistry (RSC)
          1460-4744
          0306-0012
          Jun 07 2015
          : 44
          : 11
          Affiliations
          [1 ] Laboratoire de Chimie Moléculaire, UMR CNRS 7509, SynCat, Université de Strasbourg, ECPM, 25 rue Becquerel, 67087, Strasbourg, France. wenceldelord@unistra.fr.
          Article
          10.1039/c5cs00012b
          25904287
          ea4d047f-c414-4cac-984d-35341a41dec2
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