A general entry to 2-(2-hydroxyalkyl)piperidines via iterative asymmetric dihydroxylation to cause enantiomeric enhancement

Tetrahedron Letters

Volumn 38, Issue 19, 1997, Pages 3451-3454

  Takahata, Hiroki ^a   Kubota, Minoru ^a   Momose, Takefumi ^a  

^a UNIVERSITY OF TOYAMA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; PIPERIDINE DERIVATIVE;

ARTICLE; CHIRALITY; DRUG SYNTHESIS; ENANTIOMER; IN VITRO STUDY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0030919676     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00643-6     Document Type: Article

References (27)

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24. Very recently, the same correction of the absolute configuration of (+)-8-ethylnorlobelol-I was proposed. Mill, S.; Durant, A.; Hootelé, C. Liebigs Ann. 1996, 2083.
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27. The absolute configurations of both allosedridine (11) and N-methylsedridine (12) remain unknown.