Asymmetric dihydroxylation of chiral γ-amino α,β-unsaturated esters: Turning the mismatched into the matched case via protective group tuning

Tetrahedron Letters

Volumn 37, Issue 52, 1996, Pages 9293-9296

  Reetz, Manfred T ^a   Strack, Thomas J ^a   Mutulis, Felikss ^a   Goddard, Richard ^a  

^a MAX PLANCK INSTITUT FÜR KOHLENFORSCHUNG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE; ESTER;

ARTICLE; CHIRALITY; DRUG SYNTHESIS; HYDROXYLATION; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0030599656     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)82945-0     Document Type: Article

References (21)

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10. 5. The AD-mix-β has been used in a related reaction directed toward the synthesis of (+)-lentiginosine (92 : 8 mixture of diastereomers): Gurjar, M. K.; Ghosh, L.; Syamala, M.; Jayasree, V. Tetrahedron Lett. 1994, 35, 8871.
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18. -3. Atomic coordinates and e.s.d.'s have been deposited at the Cambridge Crystallographic Data Centre.
19. -3. Atomic coordinates and e.s.d.'s have been deposited at the Cambridge Crystallographic Data Centre.
20. 3B
21. 3b