The de novo synthesis of an aceric acid thioglycoside
building block and the total synthesis of the plant carbohydrate aceric acid are described via a highly convergent
strategy. Aldol reaction of acetaldehyde and a protected
tartaric acid derivative provided the open chain carbohydrate.
Subsequent acid treatment yielded the aceric acid thioglycoside in 35% total yield over five steps. Oxidative cleavage
of the thioketal in the open chain carbohydrate and basic
hydrolysis of the methyl ester furnished fully deprotected
aceric acid in 31% yield over six steps