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Anitha Vinod

TitleClinical Associate
InstitutionUniversity of Chicago
DepartmentPediatrics-General Pediatrics
AddressChicago IL 60637
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Crich D, Vinod AU. 6-O-Benzyl- and 6-O-silyl-N-acetyl-2-amino-2-N,3-O-carbonyl-2-deoxyglucosides: effective glycosyl acceptors in the glucosamine 4-OH Series. effect of anomeric stereochemistry on the removal of the oxazolidinone group. J Org Chem. 2005 Feb 18; 70(4):1291-6. PMID: 15704963.
      View in: PubMed
    2. Crich D, Vinod AU, Picione J. The 3,4-O-carbonate protecting group as a beta-directing group in rhamnopyranosylation in both homogeneous and heterogeneous glycosylations as compared to the chameleon-like 2,3-O-carbonates. J Org Chem. 2003 Oct 31; 68(22):8453-8. PMID: 14575470.
      View in: PubMed
    3. Crich D, de la Mora M, Vinod AU. Influence of the 4,6-O-benzylidene, 4,6-O-phenylboronate, and 4,6-O-polystyrylboronate protecting groups on the stereochemical outcome of thioglycoside-based glycosylations mediated by 1-benzenesulfinyl piperidine/triflic anhydride and N-iodosuccinimide/trimethylsilyl triflate. J Org Chem. 2003 Oct 17; 68(21):8142-8. PMID: 14535796.
      View in: PubMed
    4. Crich D, Vinod AU. Oxazolidinone protection of N-acetylglucosamine confers high reactivity on the 4-hydroxy group in glycosylation. Org Lett. 2003 Apr 17; 5(8):1297-300. PMID: 12688743.
      View in: PubMed
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