1999年7月
A novel synthesis of chiral tetrahydroisoquinolines employing silyl enol ethers in the presence of chiral acyl chlorides
SYNLETT
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- 巻
- 1999
- 号
- 7
- 開始ページ
- 1154
- 終了ページ
- 1156
- 記述言語
- 英語
- 掲載種別
- 出版者・発行元
- GEORG THIEME VERLAG
6,7-Dimethoxyisoquinoline derivatives reacted with silyl enol ethers in a highly diastereoselective manner in the presence of an acyl chloride derived from L-alanine. (-)-Homolaudanosine was synthesized in an enantiopure form from 6,7-dimethoxyisoquinoline via six steps using this method.
- リンク情報
- ID情報
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- ISSN : 0936-5214
- Web of Science ID : WOS:000081954300044