𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Enantioselective synthesis of (R)-(-)-2,6-dimethyl heptanoic acid:the first application of the DITOX asymmetric building block

✍ Scribed by P.C. Bulman Page; S.M. Allin; E.W. Collington; R.A.E. Carr


Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
53 KB
Volume
35
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


8-Oxabicyclo[3.2.1]oct-6-en-3-ones: Appl
✍ Ingo V. Hartung; H. Martin R. Hoffmann πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 533 KB

## Abstract The development and design of reliable and efficient methods for the construction of chiral building blocks are crucial in modern natural product synthesis. 8‐Oxabicyclo[3.2.1]oct‐6‐en‐3‐ones are readily accessible scaffolds with defined stereochemical features which have been exploited

The first asymmetric synthesis of (2S)-
✍ Duane E. DeMong; Robert M. Williams πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 French βš– 126 KB

The first asymmetric synthesis of (2S)-, and (2R)-amino-3,3-dimethoxypropanoic acid (a-formylglycine dimethylacetal) has been achieved in two steps and 91% overall yield. The key step involved the quenching of a chiral glycine titanium enolate with trimethyl orthoformate.