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Profil bibliographique

Honggen Wang

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

457Publications signalées
11862Citations signalées
5Affiliations récentes

Les institutions déclarées

Les domaines associés

Catalytic C–H Functionalization MethodsMetal complexes synthesis and propertiesMagnetism in coordination complexesFluorine in Organic ChemistryCatalytic Cross-Coupling Reactions

Les publications récentes

2026 article OpenAlex

Photoredox/Nickel-Catalyzed Decarboxylative Monofluoromethylation of β-Boryl NHPI Esters via Radical 1,2-Boron Migration

Shuang Lin, Yifan Yang, Qingjiang Li, Shi‐Liang Huang et autres

A photoredox/nickel dual-catalyzed decarboxylative monofluoromethylation of β-boryl NHPI esters has been developed. The reaction proceeds through a radical 1,2-boron shift cascade, enabling the efficient conversion of β-boryl radicals into carbon radicals for subsequent SH2 cross-coupling with a monofluoromethyl radical. This method provides …

tw, cn (code pays fourni par la source)

0 citations Organic Letters
Accès ouvert 2026 article OpenAlex

Direct copper-catalysed deaminative cyanation of aliphatic primary amines

Jiang‐Hao Xue, Shuang Lin, J Huang, Taeseok Kang et autres

The cyano group is a versatile motif in medicinal chemistry, serving as both a target and a precursor to other functional groups. However, direct deaminative cyanation of aliphatic amines remains a challenge due to the inertness of C–N bonds and the instability …

cn, kr, us (code pays fourni par la source)

2 citations Nature Catalysis
2026 article OpenAlex

Direct Deaminative Alkynylation of Aliphatic Primary Amines

Jia-Luo Fu, Jun‐Yunzi Wu, Qi Fan, Jiang‐Hao Xue et autres

ABSTRACT Alkyl‐substituted internal alkynes are useful motifs in organic synthesis and medicinal chemistry, but their preparation from common amine precursors remains challenging. Aliphatic primary amines are widespread functional groups, yet their direct use as alkylating reagents is limited by the strength of …

cn (code pays fourni par la source)

0 citations Angewandte Chemie
Accès ouvert 2026 article OpenAlex

Direct Deaminative Alkynylation of Aliphatic Primary Amines

Jia-Luo Fu, Jun‐Yunzi Wu, Qi Fan, Jiang‐Hao Xue et autres

ABSTRACT Alkyl‐substituted internal alkynes are useful motifs in organic synthesis and medicinal chemistry, but their preparation from common amine precursors remains challenging. Aliphatic primary amines are widespread functional groups, yet their direct use as alkylating reagents is limited by the strength of …

cn (code pays fourni par la source)

2 citations Angewandte Chemie International Edition
2025 article OpenAlex

Regio‐Divergent and Stereo‐Controlled Alder‐Ene Reaction: Harnessing the Unique Electronic and Steric Properties of B(MIDA) Moiety

Jiawu Huang, Bo-Wen Xiao, Wenjin Zhang, Qingjiang Li et autres

Abstract 1,4‐Dienes are pivotal structural motifs in bioactive natural products and serve as valuable intermediates in synthetic chemistry. Among the various methods for their synthesis, the ruthenium‐catalyzed Alder‐ene reaction stands out due to its redox‐neutral, atom‐ and step‐efficient nature. However, controlling regioselectivity …

cn (code pays fourni par la source)

0 citations Angewandte Chemie
2025 article OpenAlex

Regio‐Divergent and Stereo‐Controlled Alder‐Ene Reaction: Harnessing the Unique Electronic and Steric Properties of B(MIDA) Moiety

Jiawu Huang, Bo-Wen Xiao, Wenjin Zhang, Qingjiang Li et autres

1,4-Dienes are pivotal structural motifs in bioactive natural products and serve as valuable intermediates in synthetic chemistry. Among the various methods for their synthesis, the ruthenium-catalyzed Alder-ene reaction stands out due to its redox-neutral, atom- and step-efficient nature. However, controlling regioselectivity with …

cn (code pays fourni par la source)

2 citations Angewandte Chemie International Edition
Accès ouvert 2025 preprint OpenAlex

Direct Catalytic Deaminative Cyanation of Aliphatic Primary Amines

Jiang‐Hao Xue, Shuang Lin, Jiawu Huang, Taeseok Kang et autres

The cyano group is an important and versatile functional group in medicinal chemistry. It is an important target in its own right while also serving as a precursor to other valuable motifs including aminomethyl and carboxamide groups. However, direct deaminative cyanation of …

cn, kr, us (code pays fourni par la source)

5 citations ChemRxiv
2025 article OpenAlex

Development of Indolo‐Bicyclo[3.1.1]Heptane as a Carbazole Isostere Through Radical Indolization of Bicyclo[1.1.0]Butanes

Yuan Liu, Jun‐Yunzi Wu, Shuang Lin, Fan Qi et autres

Semisaturated ring systems with a balanced fraction of C(sp3) have garnered increasing attention in drug development. In this study, we propose indolo-bicyclo[3.1.1]heptane as a potential carbazole isostere and present a novel strategy for synthesizing this new semisaturated polycyclic scaffold. The synthesis involves …

cn (code pays fourni par la source)

9 citations Angewandte Chemie International Edition
2025 article OpenAlex

Development of Indolo‐Bicyclo[3.1.1]Heptane as a Carbazole Isostere Through Radical Indolization of Bicyclo[1.1.0]Butanes

Yuan Liu, Jun‐Yunzi Wu, Shuang Lin, Fan Qi et autres

Abstract Semisaturated ring systems with a balanced fraction of C(sp3) have garnered increasing attention in drug development. In this study, we propose indolo‐bicyclo[3.1.1]heptane as a potential carbazole isostere and present a novel strategy for synthesizing this new semisaturated polycyclic scaffold. The synthesis …

cn (code pays fourni par la source)

2 citations Angewandte Chemie
2025 article OpenAlex

Selective Synthesis of Z-α-Iodostyrenes via Hydroiodination and Photochemical Manganese-Catalyzed Geometric Isomerization

Ya‐Jie Tang, Qi Fan, Shuang Lin, Qingjiang Li et autres

Alkenyl iodides are essential intermediates in organic synthesis, traditionally synthesized via hydrometalation of alkynes or direct hydroiodination, which favor the formation of E isomers. However, methods for selectively producing Z -isomers remain underdeveloped. Inspired by photoinduced manganese-mediated iodine abstraction and radical rebound …

cn, no (code pays fourni par la source)

4 citations The Journal of Organic Chemistry

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