引用本文:
Chen Xi Zhang, Li Jing Fang, Fu Qiang Bi, Yu Lin Li. An enantioselective formal synthesis of (-)-thujopsene[J]. Chinese Chemical Letters,
2008, 19(3): 256-258.
doi:
10.1016/j.cclet.2008.01.009
Citation: Chen Xi Zhang, Li Jing Fang, Fu Qiang Bi, Yu Lin Li. An enantioselective formal synthesis of (-)-thujopsene[J]. Chinese Chemical Letters, 2008, 19(3): 256-258. doi: 10.1016/j.cclet.2008.01.009
Citation: Chen Xi Zhang, Li Jing Fang, Fu Qiang Bi, Yu Lin Li. An enantioselective formal synthesis of (-)-thujopsene[J]. Chinese Chemical Letters, 2008, 19(3): 256-258. doi: 10.1016/j.cclet.2008.01.009
An enantioselective formal synthesis of (-)-thujopsene
摘要:
Dihydromayurone (3), a key intermediate to synthesize (-)-thujopsene (1), was efficient enantiocontrolled synthesized from (+)-dihydrocarvone through 9 steps in an overall yield of 19.3%. The key step was the Simmons-Smith reaction.
English
An enantioselective formal synthesis of (-)-thujopsene
Abstract:
Dihydromayurone (3), a key intermediate to synthesize (-)-thujopsene (1), was efficient enantiocontrolled synthesized from (+)-dihydrocarvone through 9 steps in an overall yield of 19.3%. The key step was the Simmons-Smith reaction.
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Key words:
- Thujopsene
- / Dihydromayurone
- / Synthesis
- / Dihydrocarvone
- / Simmons-Smith reaction
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