Intramolecular vs. intermolecular induction in the diastereoselective catalytic reduction of enantiomerically pure ketones with borane in the presence of cyclic β-amino alcohols

Tetrahedron: Asymmetry

Volumn 6, Issue 12, 1995, Pages 3063-3070

  Reiners, I ^a   Wilken, J ^a   Martens, J ^a  

^a UNIVERSITY OF OLDENBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALKANOL; CYCLOALKANOL DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0029584795     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00404-1     Document Type: Article

References (42)

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3. Asymmetric synthesis using chirally modified borohydrides. Part 2. Enantioselective reduction of ketones with polymeric (S)-prolinol?borane reagent
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5. (1S,3S,5S)-2-Amino-3-methoxymethyl-2-azabicyclo [3.3.0]octan: SAMBO — ein neuer chiraler Hilfsstoff
6. Verwertung industrieller Abfallstoffe, 4. Synthese neuer, chiraler β-Aminoalkohole und deren Anwendung in der katalytischen enantioselektiven Addition von Diethylzink an Benzaldehyd
7. Chiral catalyst controlled addition of dialkylzincs to chiral ?-siloxyaldehydes; asymmetric synthesis of either diastereoisomer of mono-protected vicinal diols
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9. Catalytic asymmetric synthesis of ?-hydroxy ketones and aromatic hydroxy ketones by the chemo- and enantio-selective alkylation of keto aldehydes with dialkylzincs
10. On the double bond isostere of the peptide bond: preparation of modified di- and tri-peptides incorporating proline and alanine analogues