Aller au contenu principal
Profil bibliographique

Shuang Lin

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

22Publications signalées
371Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Catalytic C–H Functionalization MethodsRadical Photochemical ReactionsFluorine in Organic ChemistryOxidative Organic Chemistry ReactionsOrganoboron and organosilicon chemistry

Les publications récentes

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
Accès ouvert 2025 article OpenAlex

Harnessing the β-boron effect for regioselective Ru-catalyzed hydrosilylation of internal alkynes

Jiasheng Qian, Shuang Lin, Zhihao Chen, Jiawu Huang et autres

Metal-catalyzed hydrosilylation of alkynes is recognized as a straightforward and atom economic method for synthesizing alkenylsilanes. While substantial advancements have been made with terminal alkynes, achieving precise regio- and stereocontrol with unsymmetrical internal alkynes remains a significant challenge. In this study, we …

cn (code pays fourni par la source)

4 citations Nature Communications
Accès ouvert 2025 preprint OpenAlex

Development of Indolo-Bicyclo[3.1.1]heptane as a Carbazole Isostere through Radical Indolization of Bicyclo[1.1.0]butanes

Honggen Wang, Yuan Liu, Jun‐Yunzi Wu, Fan Qi et autres

Semisaturated ring systems with a balanced fraction of Csp3 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)

1 citation ChemRxiv
Accès ouvert 2025 article OpenAlex

Saturated F 2 ‐Rings from Alkenes

Li Yin, Vadym Sham, Ivan G. Logvinenko, Shuang Lin et autres

Abstract A general method to convert simple exocyclic alkenes into saturated F 2 ‐rings has been developed. The reaction involves reagent C 6 F 5 I(OAc) 2 . The reaction efficiently works on the mg‐, g‐, and even multigram scale.

cn, ua (code pays fourni par la source)

11 citations Angewandte Chemie International Edition
2025 article OpenAlex

Saturated F 2 ‐Rings from Alkenes

Li Yin, Vadym Sham, Ivan G. Logvinenko, Shuang Lin et autres

Abstract A general method to convert simple exocyclic alkenes into saturated F 2 ‐rings has been developed. The reaction involves reagent C 6 F 5 I(OAc) 2 . The reaction efficiently works on the mg‐, g‐, and even multigram scale.

cn, ua (code pays fourni par la source)

2 citations Angewandte Chemie
Accès ouvert 2024 preprint OpenAlex

Saturated F2-rings from Alkenes

Honggen Wang, Li Yin, Xiaobin Liu, Vadym Sham et autres

A general method to convert simple exocyclic alkenes (no Ar-substituents) into saturated F2-rings has been developed. The reaction involves the IIII-reagent C6F5I(OAc)2 (F5-PIDA). The reaction efficiently works on a mg-, g-, and even multigram scale.

cn, ua (code pays fourni par la source)

0 citations ChemRxiv
2024 article OpenAlex

β-Silicon Effect Enables Metal-Free Site-Selective Intermolecular Allylic C–H Amination

Shuang Lin, Yuan Liu, Gao Kun-yu, Zhihao Chen et autres

α-Amino silanes and their derivatives play pivotal roles across diverse applications, yet their current synthetic methods often entail intricate functional group manipulations. Despite the widespread use of allyl silanes as carbon nucleophiles in organic synthesis, their participation in allylic C–H functionalization has …

cn (code pays fourni par la source)

7 citations ACS Catalysis

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.