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Volumn , Issue 11, 1999, Pages 2885-2892

A new synthetic approach toward (+)-ambruticin analogs: Preparation of a C10-C11 cis-isomer fragment

Author keywords

Alkylations; Ambruticin; Asymmetric synthesis; C Glycosylation; Carbohydrates; Palladium; Pyranose

Indexed keywords

AMBRUTICIN; CARBOHYDRATE; PALLADIUM;

EID: 0032698880     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(199911)1999:11<2885::aid-ejoc2885>3.0.co;2-j     Document Type: Article
Times cited : (20)

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    • note
    • 3), of the 1-phenyl-1,2-ethanediol so obtained was identical to that of the pure (R) enantiomer of commercial origin (Acros).
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    • [7e] (MeONa, MeOH, toluene, 60°C), failed in our hands to ensure β-epimerization of 15-α to less than a 5:95 ratio.
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    • Attempts to use Lindlar Pd catalyst failed or gave very little conversion
    • Attempts to use Lindlar Pd catalyst failed or gave very little conversion.


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