𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Highly Enantioselective Hydrogenation of 3,5-Diketo Esters: A Formal Synthesis of Tetrahydrolipstatin.

✍ Scribed by Jolanta Polkowska; Ewa Lukaszewicz; Jaroslaw Kiegiel; Janusz Jurczak


Publisher
John Wiley and Sons
Year
2004
Weight
95 KB
Volume
35
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Highly Enantioselective Transfer Hydroge
✍ Qiang Kang; Zhuo-An Zhao; Shu-Li You πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 77 KB πŸ‘ 1 views

## Abstract Chiral phosphoric acids have been identified as highly efficient organocatalysts for the asymmetric transfer hydrogenation of α‐imino esters and amide. Utilizing Hantzsch esters as the hydrogen donor, versatile highly enantioenriched α‐amino esters and their derivatives were obtained wi

A highly enantioselective rhodium cataly
✍ Dr. Felix Spindler; Ulrich Pittelkow; Hans-Ulrich Blaser πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 529 KB

The enantioselective hydrogenation of several a-keto acid derivatives with rhodium diphosphine catalysts has been investigated using a random screening approach. The neutral rhodium catalyst prepared in situ from bis(2,5norbornadiene rhodium chloride) and NORPHOS has been found to be an excellent ca