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Studies on Macrocyclic Diterpenoids (Ⅵ)——A Novel Synthetic Route to (±)-Cembrene-A

Studies on Macrocyclic Diterpenoids (Ⅵ)——A Novel Synthetic Route to (±)-Cembrene-A
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摘要 The total synthesis of(土)-cembrene-A, a termite pheromone, was achieved from geranylacetone and geraniol as starting materials. The key steps were the phase transfer catalyzed coupling reaction of sulphone (6) with chloride (9) and the intramolecular macrocyclization of dicarbonyl precursor (12) induced by low valent titanium. The synthetic route was short with anoverall yield of 17%. The total synthesis of(土)-cembrene-A, a termite pheromone, was achieved from geranylacetone and geraniol as starting materials. The key steps were the phase transfer catalyzed coupling reaction of sulphone (6) with chloride (9) and the intramolecular macrocyclization of dicarbonyl precursor (12) induced by low valent titanium. The synthetic route was short with anoverall yield of 17%.
出处 《Science China Chemistry》 SCIE EI CAS 1993年第10期1161-1166,共6页 中国科学(化学英文版)
基金 Project supported by the National Natural Science Foundation of China and by the Special Research Grant for Doctoral Sites in Universities.
关键词 SYNTHESIS MACROCYCLIC DITERPENE (±)-cembrene-A (E E E)-4 8 12-trimethyl-1-isopropenyl-3 7 11-cyclotetradecatriene. synthesis macrocyclic diterpene (±)-cembrene-A (E E E)-4 8 12-trimethyl-1-isopropenyl-3 7 11-cyclotetradecatriene.
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