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Merck
CN

Synthesis of (-)-homogalanthamine from naltrexone.

The Journal of organic chemistry (2011-03-09)
Naoshi Yamamoto, Hideaki Fujii, Satomi Imaide, Shigeto Hirayama, Toru Nemoto, Junji Inokoshi, Hiroshi Tomoda, Hiroshi Nagase
摘要

Acetylcholinesterase inhibitor (-)-homogalanthamine 3 was synthesized from μ opioid antagonist naltrexone (2) in 16% total yield. The synthesis features Grob fragmentation as a key reaction, which was especially accelerated in the presence of 15-crown-5.

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Sigma-Aldrich
15-冠醚-5, 98%