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Green chemistry method combines light and air to build key molecules for future medicines

Pioneering green chemistry: Light and air combine to build key molecules for future medicines
Enantioselective heterocoupling of 2-naphthylamines with 2-naphthol derivatives via cooperative photoactivation and chiral vanadium (V). Credit: ACS Catalysis (2025). DOI: 10.1021/acscatal.5c05038

A research group led by The University of Osaka has achieved a world-first in catalytic asymmetric synthesis, developing an innovative method for efficiently producing NOBIN, a valuable molecule used in pharmaceuticals.

Their article, "Enantioselective Heterocoupling of 2-Naphthylamines with 2-Naphthol Derivatives via Cooperative Photoactivation and Chiral Vanadium(V) Catalysis," is in ACS Catalysis.

Their approach combines a vanadium catalyst, LED light, and oxygen, drastically reducing waste by eliminating byproduct formation common in conventional methods, and establishing a highly sustainable synthetic pathway.

Many modern medicines and depend on molecules that come in "right-" and "left-handed" forms, known as chiral molecules. Traditionally, making these molecules requires multiple steps and often produces unwanted chemical waste.

In the case of NOBIN, previous methods always produced additional unwanted byproducts, reducing efficiency and increasing environmental burden.

The team's innovation lies in cooperatively combining a vanadium catalyst and light. The selectively converts 2-naphthol into a radical species. Concurrently, LED light under oxygen generates a cationic radical species from 2-naphthylamine via a charge-transfer complex.

Pioneering green chemistry: Light and air combine to build key molecules for future medicines
Representative axially chiral organic molecules: NOBIN, BINAP, BINOL, BINAM. Credit: ACS Catalysis (2025). DOI: 10.1021/acscatal.5c05038

These two radicals then efficiently couple, exclusively yielding NOBIN derivatives. This allows for an ideal 1:1 input ratio of starting materials and utilizes low-energy LED light, significantly minimizing and making the synthesis highly sustainable.

This clean process yields only water as a byproduct, showcasing exceptional environmental compatibility and waste reduction. Activating molecules using light is energy-saving and safe, accelerating next-generation asymmetric synthesis research.

Professor Shinobu Takizawa, senior author of the study states, "This achievement opens new avenues in , with applications anticipated for more and drug candidates. Cooperative catalysis, combining light and metal catalysts, embodies a sustainable chemical process. This study is a major step toward creating an environmentally harmonious future society."

More information: Duona Fan et al, Enantioselective Heterocoupling of 2-Naphthylamines with 2-Naphthol Derivatives via Cooperative Photoactivation and Chiral Vanadium(V) Catalysis, ACS Catalysis (2025).

Journal information: ACS Catalysis

Provided by University of Osaka

Citation: Green chemistry method combines light and air to build key molecules for future medicines (2025, October 22) retrieved 24 October 2025 from /news/2025-10-green-chemistry-method-combines-air.html
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