• Bulletin of the Korean Chemical Society
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• v.28 no.6
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• pp.915-916
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• 2007

• Bulletin of the Korean Chemical Society
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• v.8 no.4
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• pp.329-332
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• 1987

The reaction of (E)-1-alkenyl-1,3,2-benzodioxaboroles with a variety of allylic phenoxides in the presence of a catalytic amount of Pd$(PPh_3)_4$ is described. The reaction affords a general and simple procedure for the preparation of 1,4-alkadienes from alkynes via hydroboration.

• Archives of Pharmacal Research
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• v.25 no.1
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• pp.45-48
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• 2002

Stereoselective syntheses of ($\pm$)-epibatidine analogues 2, which contain the 8-azabicyclo[3.2.1]octane ring system, were achieved by using palladium-catalyzed cross-coupling reaction from 4 and the analgesic activity was tested by Mouse writhing antinociceptive assay.

• Archives of Pharmacal Research
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• v.25 no.1
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• pp.49-52
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• 2002

Syntheses of ($\pm$)-homoepibatidine analogues (2), which contain the 8-azabicyclo [3.2.1 ]octane ring system, were achieved by using palladium-catalyzed reductive-coupling reaction from 3 and the analgesic activity was tested by Mouse writhing antinociceptive assay

• Archives of Pharmacal Research
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• v.22 no.3
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• pp.300-301
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• 1999

Stereoselective synthesis of (${\pm}$)-epibatidine analog 2, which contains the 8-azabicyclo[3.2.1]octane ring system, was achieved by using palladium-catalyzed Heck-type coupling reaction from 3.

• 한국정보디스플레이학회:학술대회논문집
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• 2004.08a
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• pp.665-668
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• 2004

Oligothiophene derivatives have been well-known as an p-type channel material.$^1$ Here, we report novel oligothiophene derivative containing methylene linkage as an p-type channel material. Oligothiophene derivative containing methylene linkage BHTM was synthesized and characterized. BHTM was prepared by a palladium-catalyzed cross-coupling reaction via zinc-substituted thiophene. BHTM exhibited high thermal stability and at least one transition temperature.

• Journal of the Korean Chemical Society
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• v.44 no.1
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• pp.30-36
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• 2000

Upon Pd(0)-catalyzed coupling reaction of (2R)-2-(N,N-ditosylimido)-3-butenyl methyl malonate (4) which was selected for the total synthesis of A-factor, (3R)-2-(6-methylheptanoyl)-3-hydroxy methyl-4-buttinolide (1), an unexpected 14-membered cyclic compound, bis(2-methoxycabonyl-(4E)-hexenolide) (15) was obtained. The structure of this compound was conformed by X-ray crystallography. This result implies that this method can be applied the synthesis of various size of symmetrical macrocyclic compounds.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.161-161
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• 2006

New polymeric and oligomeric OTFT materials containing fused aromatics such as anthracene and naphthalene have been designed, synthesized and characterized. The new OTFT materials were prepared by palladium-catalyzed Suzuki cross-coupling reaction. The obtained materials were characterized by various spectroscopic methods such as UV-vis, PL, cyclovoltametry, and XRD. The obtained OTFT materials containing fused aromatics showed high thermal stability above $350^{\circ}C$ In OTFT devices using new materials, high charge carrier mobility and on/off ratio were observed.

• 한국정보디스플레이학회:학술대회논문집
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• 2002.08a
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• pp.471-474
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• 2002

Three-ring types liquid crystalline compounds having fluoro and isothiocyanate substituent were synthesized and their physical and electro-optical properties were measured to evaluate the applications to active matrix VA liquid crystal displays. The tetrakis(triphenylphosphine)palladium(0) catalyzed cross coupling of aryl boronic acids with aryl halides is used to prepare trans-4'-Alkoxy-2,3-difluoro-3'-isothiocyanato-4-(4-alkylcyclohexyl}-biphenyl series. The synthesized compounds showed the nematic liquid crystalline phase and the negative dielectric anisotropy. The prepared mixtures showed faster response time and lower threshold voltage than their host mixture.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.19 no.6
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• pp.558-562
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• 2006

We have synthesized a new p-type polymer, poly(9,9'-n-dioctylfluorene-alt-phenoxazine) (PFPO), via the palladium catalyzed coupling reaction. The number average molecular weight ($M_n$) of PFPO was found to be 23,000. PFPO dissolves in common organic solvents such as chloroform and toluene. The UV-visible absorption maximum of the PFPO thin film is clearly blue-shifted with respect to that of F8T2, poly-(9,9'-n-dioctylfluorene-alt-bithiophene). The introduction of the phenoxazine moiety into the polymer system results in better field-effect transistor (FET) performance than that of F8T2. A solution processed PFPO TFT device with a top contact geometry was found to exhibit a hole mobility of $2.7{\times}10^{-4}cm^2/Vs$ and a low threshold voltage of -2 V with high on/off ratio(${\sim}10^4$).