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Demonstrates efficient synthesis of arylamino alcohols via catalyst innovations, indicating novel pathways for chemical reactions.
from nitroarene reduction. Subsequent 1,3-dipolar cycloaddition of the resulting nitrones with alkenes, followed by reduction of the cycloadducts, delivers the desired products. The concept of exploiting metal-support synergy for mild reduction and efficient intermediate conversion will open a door to the further development of useful tandem reactions through rational catalyst design.
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W et al. (2026) studied this question.
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