Cyanuric chloride catalysed rapid conversion of β-ketoesters into β-enaminoesters under mild and solvent-free conditions

Kamble, Vinod T.; Joshi, Neeta S.; Atkore, Sandeep T.

doi:10.1007/bf03245892

Cited by 4 publications

(2 citation statements)

References 7 publications

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“…Kamble et al, [63] developed the solvent-free synthesis of β-enaminoesters into β-ketoesters using a cyanuric acid catalyst. The reaction involved grinding at 25 C in a mortar pestle.…”

Section: Synthesis Of 14-dihydropyridines: Hantzsch Reactionmentioning

confidence: 99%

Role of cyanuric chloride in organic synthesis: A concise overview

Sethiya

Jangid

Pradhan

et al. 2023

Journal of Heterocyclic Chem

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Cyanuric chloride, a chlorinated analog of 1,3,5‐triazine, is used as a catalyst, promoter, and activator to catalyze and initiate several reactions like Beckmann rearrangement, Lossen rearrangement, Biginelli reaction, Suzuki coupling reaction, Pictet Spengler reaction, Mannich reaction, etc. It is employed in several reactions due to its several properties like stable, non‐volatile, cost‐efficient, easy to handle, and easy commercial availability. Moreover, it is a very renowned precursor for the synthesis of triazine‐class pesticide atrazine, dyes, and crosslinking agents. Herein in this review article, the reactions initiated, catalyzed, and promoted by cyanuric chloride from 2010 to 2022 have been elaborated.

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“…Kamble et al, [63] developed the solvent-free synthesis of β-enaminoesters into β-ketoesters using a cyanuric acid catalyst. The reaction involved grinding at 25 C in a mortar pestle.…”

Section: Synthesis Of 14-dihydropyridines: Hantzsch Reactionmentioning

confidence: 99%

Role of cyanuric chloride in organic synthesis: A concise overview

Sethiya

Jangid

Pradhan

et al. 2023

Journal of Heterocyclic Chem

View full text Add to dashboard Cite

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“…Initially amine precursor, a diketone precursor and cyanuric chloride were added to an algae mortar. [140] Upon grinding the reaction was initiated. The concept was excellent for syntheses of model secondary enamino ketone.…”

Section: Synthesis Of Starting Materials and Optimization Studiesmentioning

confidence: 99%

Approaches for Transition Metal-Free Photocatalytic Oxidation Reactions

Schilling¹

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First and foremost, I would like to thank my dedicated supervisor and I would like to express my sincerest gratitude to Prof. Dr. Shoubhik Das as my doctoral thesis supervisor. He provided me the opportunity to perform research in an interesting field of chemistry and the possibilities to investigate the physical and technical aspects of our research. Secondly, I would like to thank my second supervisor Prof. Dr. Manuel Alcarazo for his kind support and crucial scientific and administrative feedback which guided me through my time of research for this thesis.

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