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This is a In Vitro Study study.

Enantioselective Catalyzed Addition of Substituted Indens to Unsaturated Epoxides

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The reaction enables the synthesis of a complex compound with ee up to 97%, demonstrating high enantioselectivity.
It utilizes (R)-1,1'-bi-2,2'-naphthotitanium diisopropoxide as a catalyst for the regioselective reaction.
This method provides a viable route for creating substituted product mixtures with moderate yields.
The findings suggest potential applications in organic synthesis and pharmaceutical chemistry.

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Catalytic method shows high enantioselectivity in synthesizing complex compounds from indens and epoxides, indicating effectiveness.

G. М. Talybov (2025) studied this question.

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