First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol

Article abstract of DOI:10.1271/bbb.65.1559

(+)-Magnostellin C, which is a tetrahydrofuran type of lignan bearing a chiral secondary benzylic hydroxy group, was stereoselectively synthesized from L-arabinose by using threo selective aldol condensation.

Full text of DOI:10.1271/bbb.65.1559

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Bioscience, Biotechnology, and Biochemistry
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First Stereoselective Synthesis of (+)-Magnostellin
C, a Tetrahydrofuran Type of Lignan Bearing a Chiral
Secondary Benzyl Alcohol
Satoshi YAMAUCHIa & Yoshiro KINOSHITAa
a College of Agriculture, Ehime University
Published online: 22 May 2014.
To cite this article: Satoshi YAMAUCHI & Yoshiro KINOSHITA (2001) First Stereoselective Synthesis of (+)-Magnostellin C, a
Tetrahydrofuran Type of Lignan Bearing a Chiral Secondary Benzyl Alcohol, Bioscience, Biotechnology, and Biochemistry,
65:7, 1559-1567, DOI: 10.1271/bbb.65.1559
To link to this article: http://dx.doi.org/10.1271/bbb.65.1559
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