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Volumn 64, Issue 11, 2000, Pages 2320-2327

Synthesis of optically active olivil type of lignan from L-Arabinose using threo-selective aldol condensation as a key reaction

Author keywords

Lignan; Olivil; Tetrahydrofuran lignan; Threo selective aldol condensation

Indexed keywords

3-HYDROXYBUTANAL; ALDEHYDE; ALDOL; ARABINOSE; BENZALDEHYDE DERIVATIVE; LIGNAN; PIPERONAL;

EID: 0034332359     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.64.2320     Document Type: Article
Times cited : (7)

References (6)
  • 1
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    • Cambridge University Press, Cambridge
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    • Ayres, D.C.1    Loike, J.D.2
  • 2
    • 0034251852 scopus 로고    scopus 로고
    • Stereoselective Model Synthesis of the Optically Active Olivil Type of Lignan from D-Xylose
    • Yamauchi, S. and Kinoshita, Y., Stereoselective Model Synthesis of the Optically Active Olivil Type of Lignan from D-Xylose. Biosci. Biotechnol. Biochem., 64, 1563-1571 (2000).
    • (2000) Biosci. Biotechnol. Biochem. , vol.64 , pp. 1563-1571
    • Yamauchi, S.1    Kinoshita, Y.2
  • 3
    • 0002502996 scopus 로고    scopus 로고
    • Stereoselective syntheses of (-)-podorhizol lignan and its derivatives: Erythro and threo preferential aldol condensation of potassium enolate from y-butyrolac-tone with alkoxybenzaldehyde
    • Yamauchi, S. and Machi, M., and Kinoshita, Y., Stereoselective syntheses of (-)-podorhizol lignan and its derivatives: erythro and threo preferential aldol condensation of potassium enolate from y-butyrolac-tone with alkoxybenzaldehyde. Biosci. Biotechnol. Biochem., 63, 1453-1462 (1999).
    • (1999) Biosci. Biotechnol. Biochem. , vol.63 , pp. 1453-1462
    • Yamauchi, S.1    Machi, M.2    Kinoshita, Y.3
  • 4
    • 0028302692 scopus 로고
    • Rapid synthesis of 5- O-(Tert-butyldiphenylsi!yl)-2-deoxy-L-ribonolactone
    • Sharma, R. and Marquez, V. E., Rapid synthesis of 5- O-(tert-butyldiphenylsi!yl)-2-deoxy-L-ribonolactone, Synth. Commun., 24, 1937-1945 (1994).
    • (1994) Synth. Commun. , vol.24 , pp. 1937-1945
    • Sharma, R.1    Marquez, V.E.2
  • 5
    • 33947085164 scopus 로고
    • Chemistry of carbanions XXIII. Use of metal complexes to control the aldol condensation
    • House, H. O., Crumrine, D. S., Teranishi, A. Y., and Olmstead, H. D., Chemistry of carbanions XXIII. Use of metal complexes to control the aldol condensation. J. Am. Chem. Soc., 95, 3310-3324 (1973).
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 3310-3324
    • House, H.O.1    Crumrine, D.S.2    Teranishi, A.Y.3    Olmstead, H.D.4
  • 6
    • 0003038220 scopus 로고
    • An efficient deprotective method for allyl-ic alcohols protected as methoxyethoxymethyl (MEM) and methoxymethyl (MOM) ethers
    • Monti, H., Leandri, G., Klos-Ringuet, M., and Corriol, C., An efficient deprotective method for allyl-ic alcohols protected as methoxyethoxymethyl (MEM) and methoxymethyl (MOM) ethers. Synth. Commun., 13, 1021-1026 (1983).
    • (1983) Synth. Commun. , vol.13 , pp. 1021-1026
    • Monti, H.1    Leandri, G.2    Klos-Ringuet, M.3    Corriol, C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.