Abstract
The strategy for the total synthesis of aurodox (1) and efrotomycin (2) and the construction of key intermediates IV-VIII are described.
Original language | English |
---|---|
Pages (from-to) | 1691-1694 |
Number of pages | 4 |
Journal | Journal of the American Chemical Society |
Volume | 107 |
Issue number | 6 |
DOIs | |
State | Published - Mar 1985 |