@article{oai:nagoya.repo.nii.ac.jp:00027049,
 author = {Watanabe, Shinya and Ishikawa, Masatsugu and Nomura, Toshimune and Fukuyama, Tohru and Yokoshima, Satoshi},
 issue = {18},
 journal = {Synlett},
 month = {Nov},
 note = {A total synthesis of lycoposerramine-R was accomplished. The synthesis featured a Claisen–Ireland rearrangement to install a two-carbon unit, and a hetero-Diels–Alder reaction to form a cyclic enol ether that reacted with an ethynyl group to construct a cis-hydrindane core containing a quaternary carbon. A 2-pyridone synthesis using 2-(phenylsulfinyl)acetamide was used to complete the synthesis., ファイル公開：2019-11-01},
 pages = {2377--2380},
 title = {Total Synthesis of Lycoposerramine-R},
 volume = {29},
 year = {2018}
}