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• W2001034693 abstract "Abstract Conjugated oligomers bearing 4,5,6,7-tetrahydro-5 S ,6 S -dioctyloxybenzothiophene as a central linkage were synthesized by Negishi's reagent ( n -Bu 2 ZrCp 2 ) promoted intramolecular cyclization of a diyne and subsequent Suzuki coupling reactions. The chirality in the central linkage originated from tartaric acid, which induced the conjugated backbone of oligomers to exhibit interesting optical activity." @default.
• W2001034693 created "2016-06-24" @default.
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• W2001034693 date "2002-04-01" @default.
• W2001034693 modified "2023-09-23" @default.
• W2001034693 title "Zr-promoted cyclization of diynes bearing C2-chirality: synthesis and properties of new chiral conjugated molecules" @default.
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• W2001034693 doi "https://doi.org/10.1016/s0040-4039(02)00520-8" @default.
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