Tribenzotriquinacenes based on regioselective bis-formylation: Optical resolution and absolute configuration of inherently chiral derivatives and synthesis of the first cyclophane-type tribenzotriquinacene dimers

Chemistry - A European Journal

Volumn 16, Issue 41, 2010, Pages 12412-12424

  Wang, Tao ^a   Hou, Qin Qing ^a   Teng, Qing Feng ^a   Yao, Xiao Jun ^a   Niu, Wen Xue ^a   Cao, Xiao Ping ^a   Kuck, Dietmar ^b  

^a LANZHOU UNIVERSITY   (China)

^b BIELEFELD UNIVERSITY   (Germany)

Author keywords

configuration determination; formylation; regioselectivity; synthetic methods; tribenzotriquinacenes

Indexed keywords

2-NAPHTHOLS; 2D-NMR SPECTROSCOPY; ABSOLUTE CONFIGURATION; BENZYLIC; CHIRAL DERIVATIVES; CONFIGURATION DETERMINATION; CYCLOPHANES; DFT CALCULATION; DIASTEREOMERIC; ELECTRONIC CIRCULAR DICHROISM; EXCITON MODELS; FLUORESCENT CHEMOSENSORS; FORMYLATION; OPTICAL RESOLUTION; REGIO-SELECTIVE; SPECIFIC ROTATIONS; SYNTHETIC METHODS; THIACYCLOPHANES; TRIBENZOTRIQUINACENES; X-RAY CRYSTALLOGRAPHIC ANALYSIS;

ALDEHYDES; CHIRALITY; COLUMN CHROMATOGRAPHY; COPYING; DICHROISM; ENANTIOMERS; ETHERS; METAL IONS; METHANOL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OLIGOMERS; PHENOLS; SULFUR COMPOUNDS;

REGIOSELECTIVITY;

EID: 78249258088     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001620     Document Type: Article

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