• Bulletin of the Korean Chemical Society
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• 제26권11호
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• pp.1881-1884
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• 2005

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2005년도 생물공학의 동향(XVI)
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• pp.281-281
• /
• 2005

• Bulletin of the Korean Chemical Society
• /
• 제15권12호
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• pp.1031-1033
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• 1994

• Bulletin of the Korean Chemical Society
• /
• 제10권6호
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• pp.547-551
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• 1989

1-Methoxypyrrole-2-carboxylic acid and its derivatives were prepared. Fridel-Crafts bromination occurs first at 4-position and then at 5-position. Acylation of 3-methyl derivative was also directed to 4-position.

• 한국생물공학회:학술대회논문집
• /
• 한국생물공학회 2005년도 생물공학의 동향(XVI)
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• pp.486-486
• /
• 2005

• Bulletin of the Korean Chemical Society
• /
• 제31권9호
• /
• pp.2709-2711
• /
• 2010

• 한국막학회:학술대회논문집
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• 한국막학회 2005년도 추계 총회 및 학술발표회
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• pp.231-233
• /
• 2005

• Bulletin of the Korean Chemical Society
• /
• 제26권3호
• /
• pp.375-376
• /
• 2005

• Bulletin of the Korean Chemical Society
• /
• 제32권3호
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• pp.783-784
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• 2011

• Bulletin of the Korean Chemical Society
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• 제13권1호
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• pp.87-91
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• 1992

The structures of the compounds, 1, 2, 3, and 4, which were precursors of analgesics, were confirmed by modern NMR techniques. The complete $^{13}C-NMR$ assignments of these systems were established by applying COLOC (COrrelated spectroscopy for LOng range Couplings), HETCOR (HETeronuclear CORrelated spectroscopy), RCT (Relay Coherence Transfer), and NOE difference spectroscopy. The limitation of COLOC approach which has been widely used recently is discussed.