260244-85-7Relevant academic research and scientific papers
Synthesis of zeaxanthin- and cryptoxanthin-β-D-glucopyranosides
Yamano, Yumiko,Sakai, Yoshitsugu,Yamashita, Satomi,Ito, Masayoshi
, p. 141 - 146 (2007/10/03)
β-Glucosidation of (3R)-3-hydroxy-β-ionone (6) was achieved in a reasonable yield by use of tetra-O-benzoyl-α-D-glucopyranosyl bromide (8 c) as a glycosyl donor and silver triflate as an activator. The resulting glucoside (9) was transformed into the β-apo-12'-carotenal (18), which was condensed with the Wittig salt (19) or (20) to provide zeaxanthin-mono-β-D- glucopyranoside (3) or cryptoxanthin-β-D-glucopyranoside (4).
