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Volumn 17, Issue 22, 2006, Pages 3070-3074

Corrigendum to "Convolutamydine A: the first authenticated absolute configuration and enantioselective synthesis". [Tetrahedron: Asymmetry 17 (2006) 3070] (DOI:10.1016/j.tetasy.2006.11.021);Convolutamydine A: the first authenticated absolute configuration and enantioselective synthesis

Author keywords

[No Author keywords available]

Indexed keywords

CONVOLUTAMYDINE A; NATURAL PRODUCT;

EID: 33845708540     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.01.031     Document Type: Erratum
Times cited : (35)

References (56)
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    • note
    • 2).
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    • For application of (-)-8-phenylmenthol to the asymmetric reactions of α-oxocarboxylates, see and references cited therein
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    • note
    • 2; (5) Otera's distannoxane-promoted transesterification; (6) BOP, DIPEA, DMAP, DMF.
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    • 2O in THF in the presence of DMAP (cat) at room temperature for 5 h (Wille, G.; Steglich, W. Synthesis 2001, 5, 759).
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    • For recent reviews of allylmetal additions, see:
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    • Denmark, S.E.1    Fu, J.2
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    • Araki, S.1    Hirashita, T.2
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    • Pirkle (R,R)-WHELK-01 column: eluant: hexane/propan-2-ol/diethylamine 20:5:0.1; flow: 1 mL/min.
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    • note
    • 2 = 0.1242) for 3134 observed reflections and 245 parameters. Supplementary crystallographic data were deposited as CCDC 622273 with the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK.
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