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Profil bibliographique

Gaonan Wang

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

50Publications signalées
626Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Crystallization and Solubility StudiesX-ray Diffraction in CrystallographyCatalytic C–H Functionalization MethodsCatalytic Alkyne ReactionsIndustrial Technology and Control Systems

Les publications récentes

2026 article OpenAlex

Ugi-Type Reaction Enables Access to Fused Imidazole Derivatives for DNA-Encoded Library Technology

Hao Guo, Zitao Li, Gaonan Wang, Biyu Zhang et autres

This study presents a DNA-compatible synthesis of diverse N-fused imidazopyridines via a catalyst-free Ugi-type multicomponent reaction using TMSCN as a functional isonitrile equivalent. The desilylation activation occurs efficiently in water without additional catalysts. The method exhibits a broad substrate scope for aldehydes …

cn (code pays fourni par la source)

2 citations Bioconjugate Chemistry
2025 article OpenAlex

DNA-Compatible Huisgen [3 + 2] Cycloaddition of In Situ Formed Nitrile Oxides with Alkenes or Alkynes to Synthesize Isoxazolines or Isoxazoles

Gaonan Wang, Xiaona Zhang, Hui Zhu, Xiaodong Shi et autres

DNA-encoded chemical library (DECL) technology is recognized as a robust screening platform for drug discovery. Developing new DNA-compatible reactions is crucial for expanding the chemical space of DECLs. Cyclization reactions, particularly those involving the formation of heterocycles, offer unique and efficient methods …

cn (code pays fourni par la source)

7 citations The Journal of Organic Chemistry
2024 article OpenAlex

DNA-Compatible Cyclization Reaction to Access 1,3,4-Oxadiazoles and 1,2,4-Triazoles

Gaonan Wang, Yu Tan, Hanzhi Zou, Xihang Sui et autres

DNA-encoded chemical library (DECL) technology is a commonly employed screening platform in both the pharmaceutical industry and academia. To expand the chemical space of DECLs, new and robust DNA-compatible reactions are sought after. In particular, DNA-compatible cyclization reactions are highly valued, as …

cn, us (code pays fourni par la source)

12 citations Organic Letters
Accès ouvert 2023 article OpenAlex

DNA-Encoded Macrocyclic Peptide Libraries Enable the Discovery of a Neutral MDM2–p53 Inhibitor

Anthony P. Silvestri, Qi Zhang, Yan Ping, Erik W. Muir et autres

Synthetic macrocyclic peptides are an emerging molecular class for both targeting intracellular protein–protein interactions (PPIs) and providing an oral modality for drug targets typically addressed by biologics. Display technologies, such as mRNA and phage display, often yield peptides that are too large …

cn, us (code pays fourni par la source)

39 citations ACS Medicinal Chemistry Letters
2021 article OpenAlex

Nickel-Catalyzed β-Regioselective Amination/Cyclization of Ynamide-Nitriles with Amines: Synthesis of Functionalized 3-Aminoindoles and 4-Aminoisoquinolines

Xin Xie, Yi Gan, Gaonan Wang, Yuanhong Liu

A highly regioselective nickel/Lewis acid catalyzed amination/cyclization of ynamide-nitriles with amines involving β-addition has been developed. The reaction offers an attractive and efficient route for the synthesis of 3-aminoindoles and 4-aminoisoquinoline derivatives. The Ts-group on the ynamide acts as a directing group …

cn (code pays fourni par la source)

17 citations Organic Letters

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