SYNTHÈSE D'α CÉTOPHOSPHONATES ET D'ESTERS D'HYDROXY MÉTHYLÈNE DIPHOSPHONATES III
✍ Scribed by Manouni, D. El; Leroux, Y.; Burgada, Et R.
- Book ID
- 118164658
- Publisher
- Taylor and Francis Group
- Year
- 1989
- Tongue
- English
- Weight
- 442 KB
- Volume
- 42
- Category
- Article
- ISSN
- 1042-6507
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Cette substance cristallise beaucoup plus facilement que le derivk bromi? corres-8 , Le produit de condensation I1 n'a pas kt6 isol6. B, Ce composb avait dkjh 6ti: prkpare par la mCthode au phosphate triargentique par Colowick, J. Biol. Chem. 124, 557 (1938). lo) Nous op6rons cette dernikre condensa
## Abstract Some new fluorinated hydroxy‐acids and hydroxy‐ethers as well as their phosphorylated derivatives are described.
## Abstract The reaction of 1‐formyl‐ethylidene‐triphenylphosphorane with __trans__‐ and __cis__‐4,8‐dimethyl‐8‐hydroxy‐deca‐4,9‐dienal (**7**) obtained from (±)‐nerolidol through a novel bromination/oxidation/debromination sequence, afforded 2,6,10‐trimethyl‐10‐hydroxy‐dodeca‐2,6‐11‐trienal **6**
## Abstract The addition of cyanohydric acid to 1,2:5,6‐di‐O‐isopropylidene‐α‐D‐__ribo__‐hexofurannos‐3‐ulose can be sterically controlled. Under kinetic conditions, the __allo__ cyanohydrine epimer is formed, under thermodynamic conditions, the __gluco__ epimer is formed. The configuration of thes