Synthesis of Acerogenin C and (+)-Acerog
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GyΓΆrgy MiklΓ³s KeserΓΌ; MihΓ‘ly NΓ³grΓ‘di; Γron SzΓΆllΓΆsy
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Article
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1998
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John Wiley and Sons
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English
β 374 KB
The macrocyclic ketone acerogenin C (3) and the correspon-steps were the selective reduction of the double bond of an Ξ±,Ξ²-unsaturated ketone (10) and macrocyclization of an iodo-ding alcohol (+)-accerogenin A (1), diarylheptanoid constituents of the maple Acer nikoense were synthesized. The key phen