Enantioenriched naphthoquinone mannich bases by organocatalyzed nucleophilic additions to in situ formed imines

Synlett

Volumn , Issue 10, 2010, Pages 1489-1492

  Ayaz, Muhammad ^a   Westermann, Bernhard ^a,b  

^a LEIBNIZ INSTITUTE OF PLANT BIOCHEMISTRY   (Germany)

^b MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

Author keywords

1,4 addition amidosulfone; Enantioselective Mannich reaction; Naphthoquinone; Organocatalysis

Indexed keywords

3 [1 [(TERT BUTOXYCARBONYL)AMINO]HEXYL] 1,4 DIOXO 1,4 DIHYDRONAPHTHALEN 2 YL ACETIC ACID; 3 [1 [[(4 METHYLPHENYL)SULFONYL]AMINO]HEXYL] 1,4 DIOXO 1,4 DIHYDRONAPHTHALEN 2 YL ACETIC ACID; 3 [1 [[(BENZYLOXY)CARBONYL]AMINO]ETHYL] 1,4 DIOXO 1,4 DIHYDRONAPHTHALEN 2 YL ACETIC ACID; 3 [1 [[(BENZYLOXY)CARBONYL]AMINO]HEXYL] 1,4 DIOXO 1,4 DIHYDRONAPHTHALEN 2 YL ACETIC ACID; BENZONITRILE; DICHLOROMETHANE; ETHER; IMINE; MANNICH BASE; NAPHTHOQUINONE; NUCLEOPHILE; TOLUENE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DRUG STRUCTURE; ENANTIOMER; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; STEREOCHEMISTRY;

EID: 77953264117     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1219946     Document Type: Article

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