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초록
An efficient approach towards the total synthesis of Taxamairin B has been accomplished within 6 steps starting from o-bromobenzylbromide 7 with 45% overall yield. Intramolecular Heck reaction works efficiently to furnish the 6-7-6 fused icetexane scaffold under hydrative condition, which on restructuring affords the key beta,gamma-enedione intermediate. The beta,gamma-double bond has been introduced by the acid catalyzed water assisted elimination of a beta-tertiary alcohol. Later, the beta,gamma-enedione on introduction of requisite unsaturation transforms into Taxamairin B.
키워드
Taxamairin; Icetaxane; Heck reaction; natural product; total synthesis; BARBIER-TYPE ALLYLATION; ASYMMETRIC HECK; EN-ROUTE; DITERPENES; CYCLIZATION; ALDEHYDES; CYCLOISOMERIZATION; DEHYDRATION
- 제목
- Generation of the Icetexane Core by Use of a Heck Strategy: Total Synthesis of Taxamairin B
- 저자
- Le, Thuy Quynh; Karmakar, Swastik; Lee, Seonmi; Chai, Uiseong; Le, Minh Hoang; Oh, Chang Ho
- 발행일
- 2019-10
- 유형
- Article
- 저널명
- CHEMISTRYSELECT
- 권
- 4
- 호
- 40
- 페이지
- 11926 ~ 11929