## Abstract [1S‐(1R\*,2S\*,3R\*)]‐3‐[[1‐(Cyclohexylmethyl)‐2,3‐dihydroxy‐5‐methylhexyl]‐amino]‐N‐[N‐(4‐morpholinosulfonyl)‐L‐ phenylalanyl]‐3‐oxo‐DL‐alanine methyl ester (PD 132002) was found to be a renin inhibitor and thus potentially useful for the treatment of hypertension. This peptidomimetic
Chemical synthesis of D,L-3-dehydrosphinganine, its C14-, C16- and C20-homologues and the resolution into the enantiomeric forms
✍ Scribed by G. Sticht; D. Lekim; W. Stoffel
- Publisher
- Elsevier Science
- Year
- 1972
- Tongue
- English
- Weight
- 767 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0009-3084
No coin nor oath required. For personal study only.
✦ Synopsis
The chemical synthesis of D,L-3-dehydrosphinganine (3-keto sphinganine) and the resolution into its optical isomers via the mandelates is described. This procedure proved to be suitable for the homologous series. The products were characterized by elementary analysis, mass-spectroscopy, IR, NMR, gas chromatography and also by their mono-, di-and triacetyl derivatives respectively.
📜 SIMILAR VOLUMES
Reaction of A 2 CO 3 (A = K, Rb) with Sn and Se in an H 2 O/CH 3 OH mixture at 115±130 °C affords the isotypic selenidostannates(IV) A 6 Sn 4 Se 11 ´x H 2 O (A = K, x = 8) 1 and 2 whose discrete [Sn 4 Se 11 ] 6± anions each contain two corner-bridged ditetrahedral [Sn 2 Se 6 ] 4± species. Similar re