Citation:
ZHANG Da-Hai, LI Xian-Guo, SON Byeng-Hwa. Stereo-chemistry of Natural Product Botrytinone[J]. Chinese Journal of Applied Chemistry,
;2008, 25(12): 1425-1429.
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In the molecule of the natural product botrytinone isolated from the metabolites of marine-derived fungus Botrytis sp.,there are three chiral centers.2D NOE spectrum and quantum chemistry calculation all confirmed that the 7-CH3 and 5-OH are on the same side and the 4-OH on the other side.On the basis of X-ray diffraction analysis,its p-bromobenzoyl derivative C21H15Br2ClO5 belongs to triclinic system with space group P-1,a=0.668 47(5) nm,b=1.218 90(9) nm,c=1.307 8(1) nm,α=83.984(1)°,β=80.366(1)°,γ=84.514(1)°,V=1.041 5(1) nm3,and Z=2,which further support its relative structure.The CD spectrum of its p-bromobenzoyl derivative shows minor Cotton effection at 243 nm(Δε-39.9).The absolute configuration was elucidated by CD exciton chirality method.Finally it was determined to be(4R,5S,6R)-4,5-dihydroxy-3-(1-hydroxyethyl)-2-cyclopenten-1-one.
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