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Sulfur-Based Synthesis Techniques
TopicLeading institutions, researchers & key papers
This cluster of papers focuses on transition-metal-catalyzed sulfur chemistry, including sulfur bond formation, catalytic coupling reactions, and the synthesis of sulfur-containing compounds. It explores applications in drug design, organic synthesis, thiolation, sulfonylation, and medicinal chemistry.
17
Works
IDs:OpenAlex
How has Sulfur-Based Synthesis Techniques's publication output changed over time?
ScholarIQpublication output · 2006–2024
Output grew0% over the shown period — from 1 works in 2006 to 1 in 2024.
1
1
1
200620222024
What are the most-cited papers on Sulfur-Based Synthesis Techniques?
ScholarIQmost cited works
Syntheses of Novel Derivatives of 2‐Acetylfuro[2,3‐a]carbazoles, Benzo[1,2‐b]‐1,4‐thiazepino[2,3‐a]carbazoles and 1‐Acetyloxycarbazole‐2‐carbaldehydes.
V. Sangeetha, Karnam Jayarampillai Rajendra Prasad
S41354064. 200667 Citations
Palladium‐Catalyzed Domino Cyclization/Direct Aminosulfonylation Between Aryl Iodides and Amines via the Insertion of Sulfur Dioxide
Haiping Lv, X. He, Lin Shen, Xuemei Zhang, Zhong Lian
S36069537. 202210 Citations
Transition-metal-catalyzed regiodivergent sulfonylation of aziridrines for the synthesis of β-amino sulfones
Qinqiong Zeng, Yujia Gong, X. He, Xuemei Zhang, Zhong Lian
S2764884854. 20249 Citations
Where is Sulfur-Based Synthesis Techniques research published, and who funds it?
ScholarIQvenues & funding sources
TOP JOURNALS
S4135406467
S3606953710
S27648848549
TOP FUNDERS
National Science Foundation—
NIH—
Wellcome Trust—
European Research Council—
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How much of the research on Sulfur-Based Synthesis Techniques is open access?
ScholarIQopen access share
0%OPEN ACCESS
Gold
0%
Green
0%
Hybrid
0%
Bronze
0%
Closed
100%
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In Situ Generation of Palladium Nanoparticles: A Simple and Highly Active Protocol for Oxygen-Promoted Ligand-Free Suzuki Coupling Reaction of Aryl Chlorides
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A simple and efficient protocol for a palladium-catalyzed ligand-free Suzuki reaction at room temperature in aqueous DMF
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