Improved stereoselective synthesis of optically active methylene lactone, key intermediate for the synthesis of 1,2-oxidized furofuran lignan, by direct α-methylenation to butanolide

Bioscience, Biotechnology and Biochemistry

Volumn 64, Issue 10, 2000, Pages 2209-2215

  Yamauchi, Satoshi ^a   Yamamoto, Nobuyuki ^a   Kinoshita, Yoshiro ^a  

^a EHIME UNIVERSITY   (Japan)

Author keywords

Furofuran lignan; Lignan; Stereoselective synthesis

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; 3 (1 (TERT BUTYLDIMETHYLSILYL)OXY 1 (2 METHOXY 4,5 METHYLENEDIOXYPHENYL)METHYL) 2 METHYLENE 4 BUTANOLIDE; 3-(1-(TERT-BUTYLDIMETHYLSILYL)OXY-1-(2-METHOXY-4,5-METHYLENEDIOXYPHENYL)METHYL)-2-METHYLENE-4-BUTANOLIDE; CARBENE; DRUG DERIVATIVE; FURAN; FURAN DERIVATIVE; GAMMA BUTYROLACTONE; HYDROCARBON; LIGNAN; METHANE;

ARTICLE; CHEMISTRY; ELECTROSPRAY MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

4-BUTYROLACTONE; DIOXOLES; FURANS; HYDROCARBONS; LIGNANS; MAGNETIC RESONANCE SPECTROSCOPY; METHANE; OXIDATION-REDUCTION; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; STEREOISOMERISM;

EID: 0034295151     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.64.2209     Document Type: Article

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