Highly Regioselective Ru(II)‐Catalyzed Hydroamination of Ynamides With Phenyl Isocyanates

A novel and efficient method for the synthesis of (Z)‐1‐(1‐(2‐oxooxazolidin‐3‐yl)‐2‐phenylvinyl)−1,3‐diphenylurea derivatives via Ru (II)‐catalyzed hydroamination of ynamides with phenyl isocyanates has been developed. This protocol features excellent regioselectivity with a wide range of substrate scopes of phenyl isocyanates and ynamides. Using this method, highly substituted oxooxazolidinyl phenylvinyl 1,3‐diphenylurea compounds were synthesized in moderate to excellent yields.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-04-22
DOI
https://doi.org/10.1002/ejoc.70468
Primary Topic
Catalytic Alkyne Reactions
Type
article
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article

Highly Regioselective Ru(II)‐Catalyzed Hydroamination of Ynamides With Phenyl Isocyanates

Shubham Jaiswal, A T Rajesh Kumar, Narender Tadigoppula
European Journal of Organic Chemistry
Catalytic Alkyne Reactions
article

Highly Regioselective Ru(II)‐Catalyzed Hydroamination of Ynamides With Phenyl Isocyanates

Shubham Jaiswal, A T Rajesh Kumar, Narender Tadigoppula
article en

Abstract

A novel and efficient method for the synthesis of (Z)‐1‐(1‐(2‐oxooxazolidin‐3‐yl)‐2‐phenylvinyl)−1,3‐diphenylurea derivatives via Ru (II)‐catalyzed hydroamination of ynamides with phenyl isocyanates has been developed. This protocol features excellent regioselectivity with a wide range of substrate scopes of phenyl isocyanates and ynamides. Using this method, highly substituted oxooxazolidinyl phenylvinyl 1,3‐diphenylurea compounds were synthesized in moderate to excellent yields.

European Journal of Organic Chemistry
Central Drug Research Institute (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 9%
Catalytic Alkyne Reactions
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