Highly diastereoselective alkylation reactions of vinylogous urethanes derived from simple tetronic acids
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (13) , 1489-1492
- https://doi.org/10.1016/s0040-4039(00)80332-9
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- The synthesis of either (+) or (−) trans-2,5-dimethylpyrrolidineTetrahedron Letters, 1987
- An enantio- and erythro-selective lithium enolate derived from a vinylogous urethane: its application as a C4 synthon to the virginiamycin M2 problemThe Journal of Organic Chemistry, 1986
- A Convenient Synthesis of 2,4(3H,5H)-Furandione (β-Tetronic Acid)Synthetic Communications, 1981