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Articles 1 - 4 of 4
Full-Text Articles in Physical Sciences and Mathematics
Reactivity-Dependent Pcr: Direct, Solution-Phase In Vitro Selection For Bond Formation, David J. Gorin, Adam S. Kamlet, David R. Liu
Reactivity-Dependent Pcr: Direct, Solution-Phase In Vitro Selection For Bond Formation, David J. Gorin, Adam S. Kamlet, David R. Liu
Chemistry: Faculty Publications
(Figure Presented) In vitro selection is a key component of efforts to discover functional nucleic acids and small molecules from libraries of DNA, RNA, and DNA-encoded small molecules. Such selections have been widely used to evolve RNA and DNA catalysts and, more recently, to discover new reactions from DNA-encoded libraries of potential substrates. While effective, current strategies for selections of bond-forming and bond-cleaving reactivity are generally indirect, require the synthesis of biotin-linked substrates, and involve multiple solution-phase and solid-phase manipulations. In this work we report the successful development and validation of reactivity-dependent PCR (RDPCR), a new method that more directly …
Chemical Modification Of Reactive Multilayered Films Fabricated From Poly(2-Alkenyl Azlactone)S: Design Of Surfaces That Prevent Or Promote Mammalian Cell Adhesion And Bacterial Biofilm Growth, Maren E. Buck, Anthony S. Breitbach, Sonja K. Belgrade, Helen E. Blackwell, David M. Lynn
Chemical Modification Of Reactive Multilayered Films Fabricated From Poly(2-Alkenyl Azlactone)S: Design Of Surfaces That Prevent Or Promote Mammalian Cell Adhesion And Bacterial Biofilm Growth, Maren E. Buck, Anthony S. Breitbach, Sonja K. Belgrade, Helen E. Blackwell, David M. Lynn
Chemistry: Faculty Publications
We report an approach to the design of reactive polymer films that can be functionalized post-fabrication to either prevent or promote the attachment and growth of cells. Our approach is based on the reactive layer-bylayer assembly of covalently crosslinked thin films using a synthetic polyamine and a polymer containing reactive azlactone functionality. Our results demonstrate (i) that the residual azlactone functionality in these films can be exploited to immobilize amine-functionalized chemical motifs similar to those that promote or prevent cell and protein adhesion when assembled as self-assembled monolayers on gold-coated surfaces and (ii) that the immobilization of these motifs changes …
Nano-Imprinted Thin Films Of Reactive, Azlactone-Containing Polymers: Combining Methods For The Topographic Patterning Of Cell Substrates With Opportunities For Facile Post-Fabrication Chemical Functionalization, Nathaniel J. Fredin, Adam H. Broderick, Maren E. Buck, David M. Lvnn
Nano-Imprinted Thin Films Of Reactive, Azlactone-Containing Polymers: Combining Methods For The Topographic Patterning Of Cell Substrates With Opportunities For Facile Post-Fabrication Chemical Functionalization, Nathaniel J. Fredin, Adam H. Broderick, Maren E. Buck, David M. Lvnn
Chemistry: Faculty Publications
Approaches to the fabrication of surfaces that combine methods for the topographic patterning of soft materials with opportunities for facile, post-fabrication chemical functionalization could contribute significantly to advances in biotechnology and a broad range of other areas. Here, we report methods that can be used to introduce well defined nano- and microscale topographic features to thin films of reactive polymers containing azlactone functionality using nanoimprint lithography (NIL). We demonstrate that NIL can be used to imprint topographic patterns into thin films of poly(2-vinyl-4,4- dimethylazlactone) and a copolymer of methyl methacrylate and 2-vinyl- 4,4-dimethylazlactone using silicon masters having patterns of grooves …
The Scope And Limitations Of Intramolecular Nicholas And Pauson-Khand Reactions For The Synthesis Of Tricyclic Oxygen- And Nitrogen-Containing Heterocycles, Kristina D. Closser, Miriam M. Quintal, Kevin M. Shea
The Scope And Limitations Of Intramolecular Nicholas And Pauson-Khand Reactions For The Synthesis Of Tricyclic Oxygen- And Nitrogen-Containing Heterocycles, Kristina D. Closser, Miriam M. Quintal, Kevin M. Shea
Chemistry: Faculty Publications
We studied the scope and limitations of a tandem intramolecular Nicholas/Pauson−Khand strategy for the synthesis of tricyclic oxygen- and nitrogen-containing heterocycles. This methodology enables conversion of simple acyclic starting materials into a series of previously unknown heterocyclic architectures. For the preparation of cyclic ethers (Z = O), tricyclic [5,6,5]- through [5,9,5]-systems (m = 1, n = 1−4) are available with the [5,7,5]- and [5,8,5]-systems amenable to quick and efficient synthesis. Tricyclic [5,7,5]- and [5,8,5]-amine-containing (Z = NTs) heterocycles can be successfully prepared. Attempts to make larger ring systems (Z = O, m = 2; Z = O, n = …