Abstract
Highly diastereoselective cyclopropanation of a chiral α,β-dehydroamino acid derivative, obtained from D-mannitol, leads to a single isomer which has been transformed into the title compound in 65% overall yield. This product can be a useful intermediate in the synthesis of enantiopure ACC derivatives. © 1994.
Original language | English |
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Pages (from-to) | 5945-5948 |
Journal | Tetrahedron Letters |
Volume | 35 |
Issue number | 32 |
Publication status | Published - 8 Aug 1994 |