86204-15-1Relevant articles and documents
DIASTEREOSELECTION IN A DIRECTED CROSSED ALDOL REACTION BETWEEN TWO POLYOXYGENATED KETONES EMPLOYING TIN(II) ENOLATES. A FACILE STEREOSELECTIVE SYNTHESIS OF ETHYL 2-C-METHYL-DL-LYXOFURANOSIDE
Stevens, Rodney W.,Mukaiyama, Teruaki
, p. 595 - 598 (2007/10/02)
Tin(II) enolates of 1,3-dihydroxy-2-propanone derivatives react with a second ketone, methyl pyruvate, under mild conditions to afford the corresponding anti-crossed aldol products in moderate to excellent yields.Facile elaboration to the branched-chain s