33746-39-3Relevant articles and documents
Synthesis of Glycoconjugated Phthalonitriles for New Phthalocyanine-Based Photosensitizers
Crucius, G?ran,Hanack, Michael,Ziegler, Thomas
, p. 263 - 302 (2015/08/03)
Excellent photophysical and photochemical properties completed by magnificent take-up rates in malignant tissues attracted a great deal of interest to the application of glycosylated and glycoconjugated phthalocyanines in photodynamic therapy. In this stu
A new approach to A/B ring analogue of eleutherobin and sarcodictyns through a sequence of highly diastereofaceselective Diels-Alder reaction and ring opening-ring closing metathesis (RO-RCM)
Malik, Chanchal K.,Hossain, Md. Firoj,Ghosh, Subrata
scheme or table, p. 3063 - 3066 (2009/10/11)
An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcodictyns is described. The key steps involve a highly diastereofaceselective Diels-Alder reaction of a dienophile containing a furanosugar moiety with cyclop
Asymmetric epoxidation catalyzed by D-glucose-derived uloses
Shing, Tony K.M,Leung, Gulice Y.C
, p. 7545 - 7552 (2007/10/03)
Three ulose catalysts (1-3) were prepared from D-glucose via an intramolecular nitrile oxide cycloaddition (INOC) as the key step. The enantioselectivity of ulose 2 and 3 in asymmetric epoxidation was poor (up to 26% ee). Ulose 1 afforded good chemical yields (up to 83% yield) and the enantiomeric excess is up to 71% for the formation of (-)-trans-stilbene oxide.