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Volumn 39, Issue 16, 2000, Pages 2948-2950

Domino Michael aldol and domino Michael Mannich reactions: Highly stereoselective synthesis of functionalized cyclohexanes

Author keywords

Aldol reactions; Asymmetric synthesis; Cyclohexanes; Domino reactions; Mannich reactions

Indexed keywords

CYCLOHEXANE; CYCLOHEXANOL; HETEROCYCLIC AMINE;

EID: 0034683042     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20000818)39:16<2948::AID-ANIE2948>3.0.CO;2-P     Document Type: Article
Times cited : (32)

References (48)
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    • Michael additions have been frequently employed as initial step in domino reactions, for example: a) F. Näf, R. Decorzant, W. Thommen, Helv. Chim. Acta 1975, 58, 1808-1812;
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    • note
    • All new compounds were fully characterized by NMR, IR, UV spectrscopy, and mass spectrometry, and gave correct combustion analyses or high-resolution mass spectra. The assignment of product configuration was accomplished by 2D and NOE-NMR data (see Supporting Information).
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    • Charged dimethylaluminum imide complexes have been proposed and spectroscopically identified, see: a) D. A. Evans, K. T. Chapman, J. Bisaha, J. Am. Chem. Soc. 1988, 110, 1238-1256;
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    • note
    • 3 addition and Swern oxidation.
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