Diastereoselective synthesis of 2-aryl-3-aminoazepanes via a novel ring- enlargement process

Tetrahedron Letters

Volumn 41, Issue 8, 2000, Pages 1179-1182

  Cutri, Sabrina ^a   Bonin, Martine ^a   Micouin, Laurent ^a   Froelich, Olivier ^a   Quirion, Jean Charles ^b   Husson, Henri Philippe ^a  

^a FACULTÉ DES SCIENCES PHARMACEUTIQUES ET BIOLOGIQUES   (France)

^b IRCOF   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AZEPINE DERIVATIVE; PIPERIDINE DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIASTEREOISOMER; REACTION ANALYSIS; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

EID: 0034685211     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)02256-X     Document Type: Article

References (16)

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11. Satisfactory spectral and analytical data were obtained for all new compounds.
12. 2/MeOH 9:1) to give aminoalcohol 11b as a colorless oil in 91% yield (0.75 g, 2.42 mmol).
13. 2O: C 52.95, H 7.78, N 10.29; found C 52.65, H 7.49, N 10.11.
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16. 20: 180.1262, found: 180.1262.