101596-81-0

Upstream product

• 7468-58-8 3-(3, 4-dimethoxyphenyl)-1-phenylpropan-1-one 
• 4087-68-7 5,6-dimethoxy-3-phenyl-2,3-dihydro-1H-inden-1-one 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 5460-32-2 1-iodo-3,4-dimethoxybenzene 
• 143825-84-7 4,4,5,5-tetramethyl-2-(1-phenylvinyl)-1,3,2-dioxaborolane 
• 59893-87-7 2-hydroxy-4,5-dimethoxyallylbenzene 
• 53744-27-7 3,4-dimethoxychalcone 

Downstream Products

• 309248-92-8 (5,6-dimethoxy-3-phenyl-1H-inden-1-yl)lithium 

Relevant academic research and scientific papers

[Pd]-Catalyzed Intermolecular Coupling and Acid Mediated Intramolecular Cyclodehydration: One-Pot Synthesis of Indenes

An efficient one-pot synthesis of indenes from simple starting materials is presented. This process involves a dual C–C bond formation through an intermolecular Heck coupling reaction followed by acid-mediated intramolecular cyclodehydration. The strategy

Synthesis of Selectively Substituted or Deuterated Indenes via Sequential Pd and Ru Catalysis

A strategy for the synthesis of functionalized indenes is presented. The readily available substituted phenols are used as starting materials in the reaction sequence composed of Pd-catalyzed Suzuki coupling and Ru-catalyzed ring-closing metathesis, thus representing a practical method for the controlled construction of functionalized indene derivatives. The methodology has been successfully applied to a broad range of substrates, producing substituted indenes in excellent yields. This approach is also utilized for the synthesis of substituted indenes selectively deuterated in position 3, which are rare in literature.

DI-AND TRI-HETEROATOM SUBSTITUTED INDENYL METAL COMPLEXES

Novel metal complexes containing at least two heteroatoms attached to an indenyl or substituted indenyl radical which is bridged by ligand group thereby forming a covalent or coordinate/covalent bond to the metal, the use of such metal complexes in the fo