抄録
A new synthetic route to clavilactone B, a naturally occurring inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase, is disclosed. The route features a sequential samarium-mediated radical cyclization-fragmentation of an indanone derivative, which provides rapid access to a 10-membered carbocyclic motif fused to an aromatic ring.
本文言語 | English |
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ページ(範囲) | 126-129 |
ページ数 | 4 |
ジャーナル | Organic Letters |
巻 | 17 |
号 | 1 |
DOI | |
出版ステータス | Published - 1月 2 2015 |
外部発表 | はい |
ASJC Scopus subject areas
- 生化学
- 物理化学および理論化学
- 有機化学