• Bulletin of the Korean Chemical Society
• /
• v.32 no.spc8
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• pp.3171-3174
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• 2011

• Journal of the Korean Society for Precision Engineering
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• v.18 no.4
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• pp.25-36
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• 2001

• Environmental Engineering Research
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• v.8 no.2
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• pp.59-71
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• 2003

• Bulletin of the Korean Chemical Society
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• v.32 no.9
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• pp.3213-3214
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• 2011

• 한국생물공학회:학술대회논문집
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• 2005.10a
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• pp.153-154
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• 2005

• Bulletin of the Korean Chemical Society
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• v.32 no.2
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• pp.693-696
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• 2011

• Proceedings of the Microbiological Society of Korea Conference
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• 2007.05a
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• pp.107-108
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• 2007

• YAKHAK HOEJI
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• v.28 no.3
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• pp.191-195
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• 1984

A ten-step synthesis of 1, 3-di-O-acetyl-5-O-benzoyl-2-deoxy-2-fluoro-D-arabino-furanose, a versatile intermediate in the synthesis of chemotherapeutically important nucleosides, was achieved from D-glucose. This procedure affords good overall yields of products and is suitable for large scale preparations.

• Bulletin of the Korean Chemical Society
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• v.30 no.11
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• pp.2777-2778
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• 2009

• YAKHAK HOEJI
• /
• v.43 no.6
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• pp.696-702
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• 1999

The first and versatile total synthesis of isopimarol diterpene has been achieved via stereoselective construction of C-13 quaternary carbon unit as a key step. Isopimarol diterpene was synthesized from the known decalone in 17% overall yield of 16 steps.