119066-77-2Relevant academic research and scientific papers
A FORMAL TOTAL SYNTHESIS OF ERYTHROMYCIN A. 1. FACILE AND STEREOSELECTIVE SYNTHESES OF ERYTHRONOLIDE A SEGMENTS BASED ON ACYCLIC STEREOCONTROL
Nakata, Tadashi,Fukui, Mineo,Oishi, Takeshi
, p. 2219 - 2222 (2007/10/02)
Two segments, corresponding to the C1-C7 and C8-C15 parts of erythronolide A, were synthesized stereoselectively from the optically active syn-α-methyl-β-hydroxy imides prepared by Zn(BH4)2 reduction of the corresponding β-keto imides.
STEREOSELECTIVE REDUCTION OF β-KETO ESTERS WITH ZINC BOROHYDRIDE. STEROSELECTIVE SYNTHESIS OF ERYTHRO-3-HYDROXY-2-ALKYLPROPIONATES
Nakata, Tadashi,Oishi, Takeshi
, p. 1641 - 1644 (2007/10/02)
Erythro-3-hydroxy-2-alkylpropionates were prepared in high stereoselectivity and in high isolated yield by zinc borohydride reduction of the corresponding β-keto esters.
