Optical resolution and application of 1-aminotetralin

Enantiomer

Volumn 3, Issue 2, 1998, Pages 181-185

  Konno, Yuki ^a   Tominaga, Tomoyuki ^a   Murata, Toru ^a   Aoki, Yoshio ^a   Nohira, Hiroyuki ^a  

^a SAITAMA UNIVERSITY   (Japan)

Author keywords

1 aminotetralin; Diastereomeric salt formation; Massoia lactone; Preferential crystallization; Resolution

Indexed keywords

1 AMINOTETRALIN; LACTONE DERIVATIVE; TETRALIN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CRYSTALLIZATION; OPTICAL RESOLUTION; PRIORITY JOURNAL;

EID: 0031795337     PISSN: 10242430     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. J. Jacques, A. Collet and S.H. Wilen, Enantiomers, Racemates, and Resolutions, Krieger Publishing Company, Florida, 1994.
2. H. Nohira, Nippon Kagaku Kaishi, 1989, 903.
3. V. Ghislandi and D. Vercesi, Farmaco Ed. Sci., 26, 1971, 474.
4. The optically active ibuprofen, (S)-(+)-9, was obtained by the resolution of (±)-9 with (S)-(-)-3-methyl-2-phenyl-1-butylamine, H. Nohira, EP 529835 (1993); CA 119:49070n (1993).
5. D. Gernez, C. R. Acad. Sci., 63, 1866, 843.
6. Th.J. Meijer, Rec. Trav. Chim. 59, 1940, 191.
7. L. Crombie, J. Chem. Soc., 1955, 2535.
8. Fragrance characters were characterized by Nippon Zeon Co., Ltd.