Atom-economical and workup-free multiparticipation of <i>p</i>-TsOH in yne-ynamide skeletal reshuffle: access to regiospecific, chemospecific, and stereospecific (<i>E</i>)-alkenyl sulfonate/ketone-tethered indoles

This work introduces a workup-free p -TsOH-initiated yne-ynamide skeletal rearrangement process for the synthesis of stereospecific E -alkenyl sulfonate-tethered and ketone-tethered indoles via heterolytic N –Csp bond cleavage.

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Publication Details

Journal
Green Chemistry
Published
2024-12-13
DOI
https://doi.org/10.1039/d4gc05876c
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.62
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article

Atom-economical and workup-free multiparticipation of p-TsOH in yne-ynamide skeletal reshuffle: access to regiospecific, chemospecific, and stereospecific (E)-alkenyl sulfonate/ketone-tethered indoles

Jeh‐Jeng Wang, T. L. Chandana, Mohana Reddy Mutra
3 citations
Green Chemistry
Fluorine in Organic Chemistry
0.62
article

Atom-economical and workup-free multiparticipation of p-TsOH in yne-ynamide skeletal reshuffle: access to regiospecific, chemospecific, and stereospecific (E)-alkenyl sulfonate/ketone-tethered indoles

Jeh‐Jeng Wang, T. L. Chandana, Mohana Reddy Mutra
article en
3 citations

Abstract

This work introduces a workup-free p -TsOH-initiated yne-ynamide skeletal rearrangement process for the synthesis of stereospecific E -alkenyl sulfonate-tethered and ketone-tethered indoles via heterolytic N –Csp bond cleavage.

Green ChemistryVol. 27(4)
Kaohsiung Medical University (TW), Kaohsiung Medical University Chung-Ho Memorial Hospital (TW)
Openalex Percentile: Top 35%
Fluorine in Organic Chemistry
0.62
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