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    <identifier>10.11922/sciencedb.889</identifier>
    <datestamp>2021-08-26T13:01:17Z</datestamp>
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  <dc:date>2021-08-26</dc:date>
  <dc:title>Data of a series of novel chiral biaryl monophosphonates</dc:title>
  <dc:identifier>doi:10.11922/sciencedb.889</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Herein, we report a highly efficient organocatalytic asymmetric arylation of p-quinone phosphonates and 2-naphthols. A series of chiral biaryl monophosphonates were obtained under mild conditions in excellent yields and enantionselectivities (up to 99% yield and 95% ee). This reaction is highly functional group tolerant and could be operated at gram scale with a low catalyst loading (0.5 mol %). Remarkably, our approach provides a green and readily access to novel chiral biaryl monophosphorus ligands. Compound 4ca was successfully converted to novel chiral biaryl monophosphorus ligands 7a, 7b and 8 with high&amp;nbsp;enantionselectivities in three steps.</dc:description>
  <dc:subject>Organocatalytic Asymmetric Arylation; Atroposelective Synthesis; Biaryl Monophosphorus Ligands</dc:subject>
  <dc:creator>Guodong Sun</dc:creator>
  <dc:creator>Zhuofei Deng</dc:creator>
  <dc:creator>Zhonghua Luo</dc:creator>
  <dc:creator>Zhongqing Wang</dc:creator>
  <dc:creator>Jiancun Zhang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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