Synthesis of substituted (S)-2-aminotetralins via ring-opening of aziridines prepared from l-aspartic acid β-tert-butyl ester

Tetrahedron

Volumn 66, Issue 46, 2010, Pages 8982-8991

  Aaseng, Jon Erik ^a   Gautun, Odd R ^a  

^a NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

Author keywords

(S) 2 Aminotetralins; Aziridine; Chiral pool; Friedel Crafts cyclisation; L Aspartic acid

Indexed keywords

2 AMINO 4 TERT BUTOXY 4 OXOBUTANOIC ACID; 2 AMINO 6 FLUORO 7 METHOXYTETRALIN; 2 AMINO 7 METHOXYTETRALIN; 2 AMINOTETRALIN DERIVATIVE; ACETIC ACID; ASPARTIC ACID; AZIRIDINE DERIVATIVE; BENZYL 2 (2 TERT BUTOXY 2 OXOETHYL)AZIRIDINE 1 CARBOXYLATE; CARBOXYLIC ACID; NAPHTHALENE; TERT BUTYL 2 (1 TOSYLAZIRIDIN 2 YL)ACETATE; UNCLASSIFIED DRUG;

ARTICLE; ENANTIOMER; FRIEDEL CRAFTS REACTION; PRIORITY JOURNAL; RING OPENING; SYNTHESIS;

EID: 77958192593     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.09.025     Document Type: Article

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