Abstract
A total synthesis of aplysiatoxin was achieved formally by construction of Kishi's intermediate 13 which carried all the stereochemistry required for the synthesis of aplysiatoxin, from four fragments described in the preceding communication.
Original language | English |
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Pages (from-to) | 5141-5142 |
Number of pages | 2 |
Journal | Tetrahedron Letters |
Volume | 32 |
Issue number | 38 |
DOIs | |
Publication status | Published - Sep 16 1991 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry