This competing continuation application describes the invention and application of novel chemical transformations for the preparation of structurally unusual carbohydrates and oligosaccharides, which are important structural components of many compounds that exhibit anticancer, antimicrobial, and immunostimulating activities. Specific chemical transformations developed by the P.l.'s laboratory which will be applied in this research include the catalytic endoselective alkynol cycloisomerization reaction, as well as electrophile-promoted glycosylations including the conceptually simple but underexploited acid-catalyzed glycosylation for the synthesis of 2-deoxyglycosides. Other metal-catalyzed processes such as internally directed Heck reactions will also be utilized in the construction of branched glycosides. These transformations are the basis for unique strategies to the syntheses of O- and C-linked oligosaccharides which have many advantages over classical methods. For instance, the efficient stereoselective synthesis of alkynyl alcohol substrates is easily applied to the construction of oligosaccharides bearing unusual stereochemical and substitution patterns, as well as the highly deoxygenated oligosaccharides present in many compounds exhibiting anticancer and other therapeutic properties. ? ? Specific aims for the next funding period include continued methodology development for siteselective and stereoselective transformations of the glycal products obtained from alkynol cycloisomerization, in the context of projects directed at: ? (1) synthesis of trisaccharide natural products bearing beta-glycosides of 2,6-dideoxyglycosides of the arabino configuration (i.e. maryal); ? (2) synthesis of the altromycin C-glycoside family of antitumor antibiotics, including determination of unassigned elements of absolute and relative stereochemistry; and ? (3) partial synthesis of degradation products of the antibiotic saccharomicin natural products, including determination of absolute stereochemistry of the individual sugar components. ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA059703-10
Application #
6759412
Study Section
Medicinal Chemistry Study Section (MCHA)
Program Officer
Lees, Robert G
Project Start
1995-04-07
Project End
2006-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
10
Fiscal Year
2004
Total Cost
$321,480
Indirect Cost
Name
Emory University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Balthaser, Bradley R; McDonald, Frank E (2009) Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins. Org Lett 11:4850-3
Fei, ZhongBo; McDonald, Frank E (2007) Stereo- and regioselective glycosylations to the bis-C-arylglycoside of kidamycin. Org Lett 9:3547-50
Koo, Bonsuk; McDonald, Frank E (2007) Fischer carbene catalysis of alkynol cycloisomerization: application to the synthesis of the altromycin B disaccharide. Org Lett 9:1737-40
Koo, Bonsuk; McDonald, Frank E (2005) Synthesis of the branched C-glycoside substructure of altromycin B. Org Lett 7:3621-4
Fei, ZhongBo; McDonald, Frank E (2005) Synthesis of the aglycones of altromycins and kidamycin from a common intermediate. Org Lett 7:3617-20
Nowroozi-Isfahani, Taraneh; Musaev, Djamaladdin G; McDonald, Frank E et al. (2005) Density Functional Study of Mo-Carbonyl-Catalyzed Alkynol Cycloisomerization: Comparison with W-Catalyzed Reaction. Organometallics 24:2921-2929