SYNTHESES OF THE TETRAHYDROFURAN SUBUNITS OF TETRONASIN AND TETRONOMYCIN

Kozo HORI; Keiichi NOMURA; Hideki KAZUNO; Eiichi YOSHII

doi:10.1248/cpb.38.1778

堀耕造, 野村敬一, 数野秀樹, 吉井英一

著者情報

キーワード: ionophore antibiotic, tetronasin, tetronomycin, synthesis, L-rhamnal, aldol reaction

ジャーナルフリー

1990 年 38 巻 6 号 p. 1778-1780

DOI https://doi.org/10.1248/cpb.38.1778

詳細

抄録

L-Rhamnal has been transformed into the tetrahydrofuran subunits (14 and 21) of tetronasin (ICI-139603) (1) and tetronomycin (2), in which the three chiral centers at the 2- and 5-positions and the methoxy-bearing carbon are of mirror image.

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