Cover Feature: Chemoselective Synthesis of <i>α,β</i> ‐Unsaturated Silyl Esters and Silyl Phosphonates over Cyclopropanation (Eur. J. Org. Chem. 39/2025)

The Cover Feature illustrates the synthesis of α,β-unsaturated silyl esters and silyl phosphonates from α-diazo esters, and α-diazo phosphonate esters with allyl trimethyl silane in the presence of a catalyst. The sun symbolizes the catalyst, [Ru(Cp)*Cl2]n, which activates the trees and the canal through which acetonitrile and allyl trimethyl silane flow. These substances are absorbed by the trees next to the canal, along with fertilizer (diazo), to produce as fruits α,β-unsaturated silyl esters at 0 °C (right) and α,β-unsaturated silyl phosphonates at 50 °C (left). More information can be found in the Research Article by C. Sivasankar and co-workers (DOI: 10.1002/ejoc.202500133).

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-10-21
DOI
https://doi.org/10.1002/ejoc.70156
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
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article

Cover Feature: Chemoselective Synthesis of α,β ‐Unsaturated Silyl Esters and Silyl Phosphonates over Cyclopropanation (Eur. J. Org. Chem. 39/2025)

Sandip Dey, Vikiho Wotsa, Chinnappan Sivasankar, Gruhapriya Jelakam
European Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
article

Cover Feature: Chemoselective Synthesis of α,β ‐Unsaturated Silyl Esters and Silyl Phosphonates over Cyclopropanation (Eur. J. Org. Chem. 39/2025)

Sandip Dey, Vikiho Wotsa, Chinnappan Sivasankar, Gruhapriya Jelakam
article en

Abstract

The Cover Feature illustrates the synthesis of α,β-unsaturated silyl esters and silyl phosphonates from α-diazo esters, and α-diazo phosphonate esters with allyl trimethyl silane in the presence of a catalyst. The sun symbolizes the catalyst, [Ru(Cp)*Cl2]n, which activates the trees and the canal through which acetonitrile and allyl trimethyl silane flow. These substances are absorbed by the trees next to the canal, along with fertilizer (diazo), to produce as fruits α,β-unsaturated silyl esters at 0 °C (right) and α,β-unsaturated silyl phosphonates at 50 °C (left). More information can be found in the Research Article by C. Sivasankar and co-workers (DOI: 10.1002/ejoc.202500133).

European Journal of Organic ChemistryVol. 28(39)
Pondicherry University (IN)
Openalex Percentile: Top 77%
Cyclopropane Reaction Mechanisms
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