𝔖 Bobbio Scriptorium
✦   LIBER   ✦

P103 a chemoenzymatic route both enantiomers of the macrocyclic lactone lasiodiplodin

✍ Scribed by Schulte, B.; Bracher, F.


Book ID
123580472
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
90 KB
Volume
2
Category
Article
ISSN
0928-0987

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


An Enantiodivergent Synthesis of Both En
✍ Bracher, Franz ;Schulte, Brigitte πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 378 KB

## Abstract The macrocyclic lactone (__S__)‐curvularin (10) and its enantiomer __ent__‐10 were prepared in an enantiodivergent manner from (__S__)‐methyl 7‐hydroxyoctanoate (4), which was easily obtained on two different ways. Esterification of 4 under either retention or inversion of the chiral ce

ChemInform Abstract: An Enantiodivergent
✍ F. BRACHER; B. SCHULTE πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 32 KB πŸ‘ 2 views

An Enantiodivergent Synthesis of Both Enantiomers of the Macrocyclic Lactone Curvularin. -An enantiodivergent synthesis of curvularin (S)-(IX) and its enantiomer is presented based on the esterification of key intermediate (S)-(V) under either retention or inversion of the chiral center leading to