摘要
α-Chamigrene (12) and β -chamigrene (15) were synthesized via a useful synthon in the synthesis of chamigrene-type sesquiterpenes, i.e., 1-methoxycarbonyl 5,5,9-trimethyl spiro[ 5, 5]undeca-1, 8-dien-3-one(6),which had been prepared from a retro-aldol rearrangement product of proto- [2 +2] photocycloadducts obtained by means of Photoaddition reaction of terpinolene with methyl 2,4-dioxopentanoate
α-Chamigrene (12) and β -chamigrene (15) were synthesized via a useful synthon in the synthesis of chamigrene-type sesquiterpenes, i.e., 1-methoxycarbonyl 5,5,9-trimethyl spiro[ 5, 5]undeca-1, 8-dien-3-one(6),which had been prepared from a retro-aldol rearrangement product of proto- [2 +2] photocycloadducts obtained by means of Photoaddition reaction of terpinolene with methyl 2,4-dioxopentanoate