Stereoselective synthesis of β-amino hydroxylamines

Tetrahedron Letters

Volumn 35, Issue 47, 1994, Pages 8765-8768

  Reetz, Manfred T ^a   Röhrig, Dirk ^b   Harms, Klaus ^b   Frenking, Gernot ^b  

^a MAX PLANCK INSTITUT FÜR KOHLENFORSCHUNG   (Germany)

^b PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYLAMINE; ISOXAZOLE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0028116566     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78492-9     Document Type: Article

References (13)

1. Stereoselektive Synthese von γ-Aminocarbonsäureestern
2. Stereoselective Synthesis of ?-Aminocarboxylates
3. Neue Wege zur Nutzung von Aminosäuren als chirale Bausteine in der organischen Synthese
4. New Approaches to the Use of Amino Acids as Chiral Building Blocks in Organic Synthesis[New Synthetic Methods(85)]
5. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines
6. Allylic 1,3-strain as a controlling factor in stereoselective transformations
7. Cycloaddition reactions of λ-amino α,β-didehydro amino acid esters: a test case for the principle of 1,3-allylic strain
8. Stealth stereocontrol: stereochemical reversal of a Michael addition reaction
9. 1,4-addition to α,β-unsaturated carbonyl compounds bearing a γ-stereocenter: A molecular mechanics model for steric interactions in the transition state.