4.8 Article

Copper-Catalyzed Diastereo- and Enantioselective Borylative Cyclization: Synthesis of Enantioenriched 2,3-Disubstituted Indolines

Journal

ORGANIC LETTERS
Volume 20, Issue 7, Pages 1798-1801

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b00246

Keywords

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Funding

  1. NSFC [21672033, 21372041]
  2. Jilin Province Natural Science Foundation [20160520140JH, 20160519003JH]
  3. Fundamental Research Funds for the Central Universities [2412017ZD001]
  4. Changbai Mountain Scholarship Program

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The development of an efficient, straightforward approach for access to a wide range of enantioenriched boron-containing 2,3-disubstituted indolines via highly chemo-, diastereo-, and enantioselective copper-catalyzed intramolecular boraylative cyclization of readily available 2-styrylimines is reported. This reaction proceeds under very mild conditions and displays a high degree of functional group compatibility. The practicability of this approach is demonstrated by a gram-scale reaction and further transformations of the chiral borylated indolines.

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