1991年11月
STEREOCONTROLLED INTRAMOLECULAR CYCLIZATION OF OMEGA-TRIBUTYLSTANNYL ETHER ALDEHYDES - SYNTHESIS OF THE 6.7.7.6 RING-SYSTEM OF POLYCYCLIC ETHERS
TETRAHEDRON LETTERS
- ,
- ,
- 巻
- 32
- 号
- 48
- 開始ページ
- 7069
- 終了ページ
- 7072
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1016/0040-4039(91)85042-4
- 出版者・発行元
- PERGAMON-ELSEVIER SCIENCE LTD
The BF3.OEt2 mediated intramolecular cyclization of the gamma-oxo-substituted allylic tin (1) having an aldehyde group at the terminus of the carbon chain proceeded in a stereocontrolled manner to give the 7-membered beta-hydroxy cyclic ether (2a) with high diastereoselectivity. This method was applied for the synthesis of the 6.7.7.6 ring system (3a).
- リンク情報
- ID情報
-
- DOI : 10.1016/0040-4039(91)85042-4
- ISSN : 0040-4039
- CiNii Articles ID : 80006220984
- Web of Science ID : WOS:A1991GU56800021