1.
J Org Chem
; 79(3): 1100-10, 2014 Feb 07.
Article
in English
| MEDLINE
| ID: mdl-24410364
ABSTRACT
A new strategy for diversity-oriented direct glycosylation of bioactive small molecules was developed. This reaction features (−)-ß-pinene as acid scavenger and work with glycosyl iodides under mild conditions. With the aid of RP-HPLC and chiral SFC separation techniques, the new direct glycosylation proved effective at gram scale on bioactive small molecules including AZD6244, podophyllotoxin, paclitaxel, and docetaxel. Interesting glycoside derivatives were efficiently created with good yields and 1,2-cis selectivity.