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...

पूर्ण विवरण

ग्रंथसूची विवरण
मुख्य लेखकों: Dixon, D, Guarna, A, Ley, S, Polara, A, Rodriguez, F
स्वरूप: Journal article
भाषा:English
प्रकाशित: 2002
विवरण
सारांश: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.