Pragmatic Access\nto Hybrid Quinoxaline Scaffold Mediated\nby Elemental Sulfur Enabling Actualization to π‑Extended\nand Aza-Annulated Heterocyclic Units

A metal-free approach for synthesizing hybrid quinoxaline\nderivatives\nfrom sulfoxonium ylide and a 1,5-bis-nucleophilic N-heterocycle mediated\nby elemental sulfur is presented to illuminate the [5+1] cascade cyclization\nsequence. Large-scale synthesis and postsynthetic functionalizations\nfor the annulative π-extension and intramolecular aza-annulation\nreactions reveal the potential utility and actualize the fabricated\napproach.

Publication Details

Journal
Figshare
Published
2024-09-27
DOI
https://doi.org/10.1021/acs.joc.4c01972.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Pragmatic Access\nto Hybrid Quinoxaline Scaffold Mediated\nby Elemental Sulfur Enabling Actualization to π‑Extended\nand Aza-Annulated Heterocyclic Units

Figshare
Mycorrhizal Fungi and Plant Interactions
article

Pragmatic Access\nto Hybrid Quinoxaline Scaffold Mediated\nby Elemental Sulfur Enabling Actualization to π‑Extended\nand Aza-Annulated Heterocyclic Units

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Abstract

A metal-free approach for synthesizing hybrid quinoxaline\nderivatives\nfrom sulfoxonium ylide and a 1,5-bis-nucleophilic N-heterocycle mediated\nby elemental sulfur is presented to illuminate the [5+1] cascade cyclization\nsequence. Large-scale synthesis and postsynthetic functionalizations\nfor the annulative π-extension and intramolecular aza-annulation\nreactions reveal the potential utility and actualize the fabricated\napproach.

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Mycorrhizal Fungi and Plant Interactions
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Pragmatic Access\nto Hybrid Quinoxaline Scaffold Mediated\nby Elemental Sulfur Enabling Actualization to π‑Extended\nand Aza-Annulated Heterocyclic Units · Figshare (2024) | TGRS Research Map | TGRS