2005
DOI: 10.1002/chin.200535068
|View full text |Cite
|
Sign up to set email alerts
|

Second‐Generation Organocatalysts for the Highly Enantioselective Dynamic Kinetic Resolution of Azlactones.

Abstract: Aminocarboxylic acids (hydrazinocarboxylic acids) and esters P 0270Second-Generation Organocatalysts for the Highly Enantioselective Dynamic Kinetic Resolution of Azlactones. -After screening a series of bifunctional organocatalysts of the thiourea-tert.-amine-type, a system is found, which effect the alcoholytic dynamic kinetic resolution of azlactones (I) with up to 95% enantioselectivity. -(BERKESSEL*, A.; MUKHERJEE, S.; CLEEMANN, F.; MUELLER, T. N.; LEX, J.; Chem.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2009
2009
2009
2009

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 1 publication
0
1
0
Order By: Relevance
“…Several strategies involving enzymes, Ti-based complexes, cyclic dipeptides, and chiral DMAP nucleophilic catalysts have been employed to bring about the selective DKR of azlactones [44]. Several strategies involving enzymes, Ti-based complexes, cyclic dipeptides, and chiral DMAP nucleophilic catalysts have been employed to bring about the selective DKR of azlactones [44].…”
Section: Dynamic Kinetic Resolution Of Racemic Azlactonesmentioning
confidence: 99%
“…Several strategies involving enzymes, Ti-based complexes, cyclic dipeptides, and chiral DMAP nucleophilic catalysts have been employed to bring about the selective DKR of azlactones [44]. Several strategies involving enzymes, Ti-based complexes, cyclic dipeptides, and chiral DMAP nucleophilic catalysts have been employed to bring about the selective DKR of azlactones [44].…”
Section: Dynamic Kinetic Resolution Of Racemic Azlactonesmentioning
confidence: 99%