Abstract
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.
Original language | English |
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Pages (from-to) | 7893-7897 |
Number of pages | 5 |
Journal | Tetrahedron Letters |
Volume | 42 |
Issue number | 44 |
DOIs | |
Publication status | Published - Oct 29 2001 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Drug Discovery
- Organic Chemistry