Asymmetric Synthesis via Acetal Templates. 14.1 Preparation of Enantiomerically Pure (3S,4S)- and (3S,4R)-Statine Derivatives
Open Access
- 1 January 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (52) , 6535-6538
- https://doi.org/10.1016/s0040-4039(00)96906-5
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Synthetic studies of didemnins. II. Approaches to statine diastereomersTetrahedron Letters, 1987
- Stereospecific synthesis of N-protected statine and its analogues via chiral tetramic acidJournal of the Chemical Society, Perkin Transactions 1, 1987
- Asymmetric synthesis via acetal templates. 13. Preparation of aldol compounds from butane-1,3-diol acetalsThe Journal of Organic Chemistry, 1987
- Chiral synthesis of statineTetrahedron Letters, 1985
- Pepstatin-derived inhibitors of aspartic proteinases. A close look at an apparent transition-state analog inhibitorJournal of Medicinal Chemistry, 1985
- Cram rule selectivity in the Lewis acid catalyzed cyclocondensation of chiral aldehydes. A convenient route to chiral systems of biological interestThe Journal of Organic Chemistry, 1982
- Biologically active peptides and their mass spectraPure and Applied Chemistry, 1982
- Synthesis of (3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid derivatives. Analysis of diastereomeric purityThe Journal of Organic Chemistry, 1978
- The Stereoselective Synthesis of threo-3-Hydroxy-4-amino AcidsBulletin of the Chemical Society of Japan, 1976
- PEPSTATIN, A NEW PEPSIN INHIBITOR PRODUCED BY AGTINOMYGETESThe Journal of Antibiotics, 1970