- A stereoselective synthesis of anti-gamma,delta-alkynyl- and -alkenyl-beta-hydroxy-alpha-amino esters from tin(II) enolates of glycinate.
A stereoselective synthesis of anti-gamma,delta-alkynyl- and -alkenyl-beta-hydroxy-alpha-amino esters from tin(II) enolates of glycinate.
Chemical communications (Cambridge, England) (2003-11-05)
Jonathan J Gridley, Michael P Coogan, David W Knight, K M Abdul Malik, Christopher M Sharland, Jirada Singkhonrat, Siân Williams
PMID14594275
RESUMEN
Condensations between the tin(II) enolate 11 of ethyl N-tosylglycinate and conjugated ynals 12 and ynones 14 are highly diastereoselective, in favour of the anti-isomers 13 and 15; similar reactions of enals and enones 17 show lower but still useful levels of anti-stereoselectivity.
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