(-)-Semivioxanthin, A New Abscisic Active Compound against Hinoki Cypress Leaves Isolated from Cryptosporiopsis abietina

Author:

YADA Hiroshi,SATO Hiroji,TOSHIMA Hiroaki,DEURA Megumi,ICHIHARA Akitami

Publisher

Oxford University Press (OUP)

Subject

Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology

Reference2 articles.

1. 5) CD data for Compound 1: CD (5% dioxane in cyclohexane) λext270 nm (Δε +9.45), 247 (-1.03), 222 (+8.03); for semivioxanthin (reference 4): CD (5% dioxane in cyclohexane) λext270 nm (Δε -8.18), 248 (+1.67), 222 (-7.79).

2. 6) Synthetic (3S)-semivioxanthin methyl ether (which has the same stereochemistry as that of compound 1), [α]25D-18.0° (c 0.3, CHCl3): Deshpande, V.H., Veena Rai, and Khan, R.A., Simple syntheses of (+)-orthosporin and (-)-semivioxanthin methyl ether. Tetrahedron, 52, 7159-7162 (1996).

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