抄録
A convergent synthesis of the C1–C13 segment of amphidinolide N, a potent cytotoxic marine macrolide isolated from the dinoflagellate Amphidinium sp., was achieved. The key features of the synthesis involve vinylogous Mukaiyama and Evans aldol reactions to form the C1–C7 and C8–C13 fragments, and convergent union of the two fragments by means of an aldol reaction to construct the C1–C13 segment.
本文言語 | English |
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ページ(範囲) | 3532-3534 |
ページ数 | 3 |
ジャーナル | Tetrahedron Letters |
巻 | 57 |
号 | 31 |
DOI | |
出版ステータス | Published - 2016 1 1 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry