Cover Feature: Synthesis of β‐Enamino Sulfoxides via <i>Cine</i> ‐Substitution of 1‐Chlorovinyl <i>p</i> ‐Tolyl Sulfoxides with Lithium Amides (Adv. Synth. Catal. 14/2026)

Desulfinylation Molecules spiral inward along a logarithmic trajectory, symbolizing the transformation of 1-chlorovinyl p-tolyl sulfoxides through a complex reaction pathway. The converging spiral highlights the selective formation of ɞ-enamino sulfoxides, while emphasizing the mechanistic progression from starting materials to the central target product. More in the Research Article (10.1002/adsc.70584), Tsutomu Kimura and co-workers.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-07-16
DOI
https://doi.org/10.1002/adsc.70670
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
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article

Cover Feature: Synthesis of β‐Enamino Sulfoxides via Cine ‐Substitution of 1‐Chlorovinyl p ‐Tolyl Sulfoxides with Lithium Amides (Adv. Synth. Catal. 14/2026)

Tsutomu Kimura, Takahiro Tsuru, Masataka Ogasawara, Tsuyoshi Satoh et al.
Advanced Synthesis & Catalysis
Synthesis and Characterization of Pyrroles
article

Cover Feature: Synthesis of β‐Enamino Sulfoxides via Cine ‐Substitution of 1‐Chlorovinyl p ‐Tolyl Sulfoxides with Lithium Amides (Adv. Synth. Catal. 14/2026)

Tsutomu Kimura, Takahiro Tsuru, Masataka Ogasawara, Tsuyoshi Satoh, Rio Dohira
article en

Abstract

Desulfinylation Molecules spiral inward along a logarithmic trajectory, symbolizing the transformation of 1-chlorovinyl p-tolyl sulfoxides through a complex reaction pathway. The converging spiral highlights the selective formation of ɞ-enamino sulfoxides, while emphasizing the mechanistic progression from starting materials to the central target product. More in the Research Article (10.1002/adsc.70584), Tsutomu Kimura and co-workers.

Advanced Synthesis & CatalysisVol. 368(14)
Tokyo University of Science (JP)
Openalex Percentile: Top 16%
Synthesis and Characterization of Pyrroles
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