• Bulletin of the Korean Chemical Society
• /
• v.30 no.11
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• pp.2519-2520
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• 2009

• Bulletin of the Korean Chemical Society
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• v.30 no.12
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• pp.2935-2937
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• 2009

Asymmetric glycolate alkylation reactions in the solid phase were investigated for the first time with good stereoselectivities being obtained by using a Wang resin supported 2-imidazolidinone chiral auxiliary.

• Bulletin of the Korean Chemical Society
• /
• v.32 no.12
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• pp.4163-4164
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• 2011

• Bulletin of the Korean Chemical Society
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• v.24 no.9
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• pp.1239-1240
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• 2003

• Bulletin of the Korean Chemical Society
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• v.23 no.10
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• pp.1487-1489
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• 2002

• Bulletin of the Korean Chemical Society
• /
• v.32 no.11
• /
• pp.4133-4136
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• 2011

• Proceedings of the PSK Conference
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• 2002.10a
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• pp.345.3-346
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• 2002

In connection with the asymmetric synthesis of chiral l.2-diol. we report here the total synthesis of (＋)-frontalin using diastereoselective alkylation featuring tridentate chelation-controlled asymmetric alkylation of a-hydroxyketone, in which the chiral auxiliary is attached to the hydroxyl group as ether linkage. The starting D-glyceraldehyde acetonide was converted (S)- ［(4R)-2.2-dimethyH,3-dioxolan-4-yl］ (4-methoxyphenyl) methanol. (omitted)

• Journal of the Korean Chemical Society
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• v.60 no.5
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• pp.374-377
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• 2016

• Bulletin of the Korean Chemical Society
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• v.25 no.1
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• pp.143-146
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• 2004

• Bulletin of the Korean Chemical Society
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• v.27 no.5
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• pp.773-775
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• 2006