Synthetic Studies of Polycyclic Terpenoids Using the Intramolecular Aldol-Type Cyclization Reaction
この論文をさがす
説明
<p>Our four recent synthetic studies of polycyclic terpenoids using the intramolecular aldol type cyclization reaction are described. (i) Asymmetric total synthesis of tricyclic diterpenoid spirocurcasone using an intramolecular aldol condensation to construct the bicyclic ring system. (ii) Total synthesis of tricyclic sesquiterpenoid albaflavenone using sequential intramolecular aldol condensations to construct its tricyclic framework. (iii) Total synthesis of paralemnolide A using an intramolecular Reformatsky-Honda reaction to construct the tricyclic framework. (iv) Synthetic study of marine diterpenoid aberrarone using a repeated 1,4-addition followed by intramolecular aldol reaction protocol to construct the tetracyclic framework.</p>
収録刊行物
-
- 有機合成化学協会誌
-
有機合成化学協会誌 77 (11), 1086-1095, 2019-11-01
公益社団法人 有機合成化学協会
- Tweet
キーワード
詳細情報 詳細情報について
-
- CRID
- 1390845702318369792
-
- NII論文ID
- 130007742550
-
- NII書誌ID
- AN0024521X
-
- ISSN
- 18836526
- 00379980
-
- NDL書誌ID
- 030109885
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- NDL
- Crossref
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可