摘要
Synthetic studies toward the total synthesis of kaitocephalin 1, whose stereochemical assignment was undetermined at the time of commencement, were undertaken in an attempt to provide a general methodology to gain access to any one of all 32 possible stereoisomers. An interesting, unexpected, result was observed in the anticipated stereoselective key aldol reaction.
| 源语言 | 英语 |
|---|---|
| 页（从-至） | 7893-7897 |
| 页数 | 5 |
| 期刊 | Tetrahedron Letters |
| 卷 | 42 |
| 期 | 44 |
| DOI | |
| 出版状态 | 已出版 - 29 10月 2001 |
| 已对外发布 | 是 |