Synthesis of the dipeptide hydroxyethylene isostere of Leu-Val, a transition state mimic for the control of enzyme function
- 1 September 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (19), 4503-4508
- https://doi.org/10.1021/jo00254a016
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- A short, stereoselective synthesis of the lactone precursor to 2R,4S,5S hydroxyethylene dipeptide isosteresThe Journal of Organic Chemistry, 1986
- Synthesis and reduction of α-amino ketones derived from leucineJournal of the Chemical Society, Perkin Transactions 1, 1985
- A stereocontrolled synthesis of hydroxyethylene dipeptide isosteres using novel, chiral aminoalkyl epoxides and .gamma.-(aminoalkyl)-.gamma.-lactonesThe Journal of Organic Chemistry, 1985