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1.
Org Biomol Chem ; 15(3): 581-583, 2017 Jan 18.
Article in English | MEDLINE | ID: mdl-28000831

ABSTRACT

We report a new method to formylate phenol derivatives using formamidine acetate and acetic anhydride. This general-purpose transformation is a significant improvement over many other methods and does not require high temperatures or the addition of strong acid or base. Mono-, di-, and tri-formylated product can be obtained, depending on the substrate and conditions used.

2.
J Org Chem ; 80(10): 5144-50, 2015 May 15.
Article in English | MEDLINE | ID: mdl-25906051

ABSTRACT

We have discovered a surprising, mild method for deuteration of select aromatic compounds that is facilitated by a keto-enamine tautomeric intermediate. The mechanism of the reaction has been studied using kinetics experiments and detailed computational analysis. It was found that a chain of water molecules has a substantial role in lowering the activation barrier to the tautomerization-enhanced deuteration reaction. Our results demonstrate that tautomeric forms of aromatic molecules can be exploited to bring about enhanced reactivity.

3.
J Biomater Sci Polym Ed ; 22(11): 1427-42, 2011.
Article in English | MEDLINE | ID: mdl-20594419

ABSTRACT

Engineering of well-organized tissue constructs is active in the field of material science for biomedical applications. Here, we propose a method for orienting collagen in transparent high-density collagen hydrogels using a simple rolling method. Structural organization and mechanical function were adjusted by regulating the thickness of the construct and the cross-linking reagent. Directionality of collagen alignment on the microscopic scale was achieved parallel to the extensional flow. The preferential alignment of collagen significantly affected the mechanical properties of the construct, with strong tensile strength in the direction parallel to the collagen, and high elastic strain in the perpendicular direction. The tensile strength in the parallel direction was effectively increased by 67% by increasing the cross-linking reagents by 33%, without affecting transparency which remained at 70-80% to visible light. The constructs exhibit good biocompatibility for as a substrate for the expansion of corneal epithelial cells isolated from human donor cornea, indicating the potential for tissue engineering and biomedical applications, particularly for ocular treatments.


Subject(s)
Collagen/chemistry , Epithelium, Corneal/cytology , Hydrogels/chemistry , Mechanical Phenomena , Tissue Scaffolds/chemistry , Animals , Anisotropy , Biomechanical Phenomena , Cross-Linking Reagents/pharmacology , Humans , Tensile Strength
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