Highly diastereoselective ketone aldol reactions of butane-2,3-diacetal desymmetrised glycolic acid

Butane-2,3-diacetal (BDA) desymmetrised glycolic acid building block 1 undergoes highly diastereoselective lithium enolate ketone aldol reactions with a range of methyl and mono-substituted methyl ketones to yield, after acid-catalysed deprotection, enantiopure α,β-dihydroxy acid derivatives bearing...

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গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Dixon, D, Guarna, A, Ley, S, Polara, A, Rodriguez, F
বিন্যাস: Journal article
ভাষা:English
প্রকাশিত: 2002
বিবরন
সংক্ষিপ্ত:Butane-2,3-diacetal (BDA) desymmetrised glycolic acid building block 1 undergoes highly diastereoselective lithium enolate ketone aldol reactions with a range of methyl and mono-substituted methyl ketones to yield, after acid-catalysed deprotection, enantiopure α,β-dihydroxy acid derivatives bearing a quaternary carbon atom at the β-hydroxy centre.