Auxiliary-controlled stereoselective enolate protonation: Enantioselective synthesis of cis and trans annulated decahydroquinoline alkaloids

Tetrahedron Letters

Volumn 39, Issue 43, 1998, Pages 7835-7838

  Weymann, Markus ^a   Schultz Kukula, Martin ^a   Kunz, Horst ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; COPPER DERIVATIVE; DECAHYDROQUINOLINE DERIVATIVE; PUMILIOTOXIN C; UNCLASSIFIED DRUG;

ARTICLE; DIASTEREOISOMER; DRUG SYNTHESIS; PROTON TRANSPORT; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0032558663     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01745-6     Document Type: Article

References (18)

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16. 3, z = 8, F(000) = 3088; Turbo CAD 4, Mo-Kγ, SIR 92, SHELXL - 93. We thank Dr. D. Schollmeyer, Institut für Organische Chemie, Universität Mainz, for the X-ray analysis and for the calculations. Further details of the crystal structure analysis are available on request from the Fachinformationszentrum Karlsruhe GmbH, D-76344 Eggenstein-Leopoldshafen (Germany), on quoting the deposit number CSD-380168, the names of the authors and journal citation.
17. (11) Comins, D. L.; Dehghani, A.; J. Org. Chem. 1995, 60, 794.
18. 8a,8 = 4.1 Hz, 1H, H-8a); FD-MS: m/z (cation) = 195.8 (calc. 196.2).