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Profil bibliographique

Si-Jing Jiang

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

7Publications signalées
42Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Fluorine in Organic ChemistryAsymmetric Synthesis and CatalysisToxic Organic Pollutants ImpactInfluenza Virus Research StudiesCatalytic C–H Functionalization Methods

Les publications récentes

2026 article OpenAlex

Synthesis of Oxygen‐Based Isoquinolinium 1,4‐Zwitterions and Their Application in the Synthesis of Pyrrolo[2,1‐ a ]isoquinolines

Hong-Yuan Cao, Tian‐Ming Liao, Zhen‐Mei Chen, Si-Jing Jiang et autres

A 1,3‐dipolar [3 + 2] cycloaddition/rearrangement cascade process of α ‐alkynyl trifluoromethyl sulfoxides with isoquinoline N ‐oxides toward oxygen‐based isoquinolinium 1,4‐zwitterions bearing a trifluoromethylsulfinyl group is presented. The reaction is readily scalable, and the resulting 1,4‐zwitterions exhibit good bench stability. Furthermore, these …

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0 citations Advanced Synthesis & Catalysis
2025 article OpenAlex

A metal-free sigmatropic rearrangement/cyclization/aromatization cascade reaction of hydroxy/aminophenyl propargyl alcohols with fluoroalkanesulfinyl chlorides: synthesis of 3-fluoroalkanesulfonyl benzofurans and indoles

Si-Jing Jiang, Zhao-Zhao Li, Lina Yang, Ming Bian et autres

A metal-free protocol to synthesize 2-alkyl-3-fluoroalkanesulfonyl benzofurans and indoles from o -hydroxyphenyl/ o -aminophenyl propargyl alcohols and fluoroalkanesulfinyl chlorides (R F SOCl) was disclosed.

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3 citations Organic Chemistry Frontiers
2023 article OpenAlex

Synthesis of 2-acyl benzofurans and indoles based on nucleophile-intercepted Meyer–Schuster rearrangement of o -hydroxyphenyl and o -aminophenyl propargylic alcohols

Zhao-Zhao Li, Si-Jing Jiang, Shu-Yun He, Yu‐Ning Gao et autres

A new type of nucleophile-intercepted Meyer–Schuster rearrangement mediated by pyridine N -oxide under metal-free conditions using a catalytic amount of acid is disclosed. It enables synthesis of 2-acyl benzofurans and indoles in 56–>99% yields.

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15 citations Organic Chemistry Frontiers

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