Advanced search

Filter By:

Journal Check one or more journals to show results from those journals only.

Choose more journals

Article type Check one or more article types to show results from those article types only.
Subject Check one or more subjects to show results from those subjects only.
Date Choose a date option to show results from those dates only.

Custom date range

Clear all filters
Sort by:
Showing 1–4 of 4 results
Advanced filters: Author: Baoquan Zhan Clear advanced filters

  • Despite the growing demand for optically active boron dipyrromethenes (BODIPYs), which are useful in live cell imaging, photodynamic therapy, and fluorescent materials science, the synthesis of chiral 3-amino-BODIPYs remains a challenge. Herein, the authors report the first synthesis of boron-stereogenic 3-amino-BODIPYs via a palladium-catalyzed desymmetric C–N cross-couplings.

    • Baoquan Zhan
    • Li-Qing Ren
    • Chuan He
    ResearchOpen Access
    Nature Communications
    Volume: 16, P: 1-8

  • Even though chiroptical luminophores have high potential for optoelectronic innovation and precision bioimaging, their rational engineering remains constrained by synthetic limitations. Here, the authors report a streamlined and programmable asymmetric synthesis platform enabling systematic construction of boron-stereogenic boron dipyrromethenes (BODIPYs) with near-infrared chiroptical activity.

    • Jiayi Zhao
    • Li-Qing Ren
    • Chuan He
    ResearchOpen Access
    Nature Communications
    Volume: 16, P: 1-10

  • Boron dipyrromethenes (BODIPYs) have found widespread applications owing to their spectroscopic and photophysical properties, but strategies for the synthesis of enantioenriched boron-stereogenic BODIPYs are lacking. Now a modular enantioselective assembly of multi-substituted boron-stereogenic BODIPYs via a Pd-catalysed desymmetric Suzuki coupling has been developed, giving access to a range of highly functionalized chiral BODIPYs.

    • Li-Qing Ren
    • Baoquan Zhan
    • Chuan He
    Research
    Nature Chemistry
    Volume: 17, P: 83-91