2001年5月21日
Synthesis of the J ring segment of gambieric acid
Tetrahedron Letters
- ,
- ,
- 巻
- 42
- 号
- 21
- 開始ページ
- 3649
- 終了ページ
- 3651
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1016/S0040-4039(01)00530-5
The J ring segment 2 of gambieric acid was synthesized stereoselectively by the coupling between the cyclic ether component 3 and the alkenyl iodide 4. The tetrahydropyran 3 was stereoselectively synthesized by the 6-endo-cyclization of a hydroxyepoxide prepared from deoxy-D-ribose. The side chain moiety 4 was prepared by the stereoselective hydrostannation of an internal alkyne. © 2001 Elsevier Science Ltd. All rights reserved.
- リンク情報
- ID情報
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- DOI : 10.1016/S0040-4039(01)00530-5
- ISSN : 0040-4039
- CiNii Articles ID : 80012323430
- SCOPUS ID : 0035926268