Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mary S. Gin"'
Autor:
Nandita Madhavan, Mary S. Gin
Publikováno v:
ChemBioChem. 8:1834-1840
Ion-channel mimics are able to transmit electrical signals across phospholipid membranes, and can be envisioned as nanoswitches for molecular electronics. Here, we reported the use of pH to alter ion-transport rates through a synthetic aminocyclodext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26565d05312ce4a66d47842e70128e4a
https://doi.org/10.1002/cbic.200700321
https://doi.org/10.1002/cbic.200700321
Publikováno v:
Angewandte Chemie. 117:7756-7759
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48704d77ef742d72f092407c029e5cfb
https://doi.org/10.1002/ange.200501625
https://doi.org/10.1002/ange.200501625
Autor:
Mary S. Gin, Rachel S. Hector
Publikováno v:
Supramolecular Chemistry. 17:129-134
This review discusses recent advances in mimicry of transmembrane ion channel proteins using artificial systems. While modified protein channels and surface-functionalized nanoporous membranes are covered briefly, the primary focus is on synthetic io
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7677ce65c6cd99af138ba7fa5ad6af20
https://doi.org/10.1080/10610270412331328871
https://doi.org/10.1080/10610270412331328871
Publikováno v:
Synthesis. :3084-3088
A new iterative route to substituted acenes is reported that centers on regioselective cycloaddition of a nickel-benzyne and 1-trimethylsilyl-1,3-pentadiyne. The five-step sequence installs two fused aromatic rings and two methyl substituents onto th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f821d5814948d3ffc48abfad584936b
https://doi.org/10.1055/s-2004-834894
https://doi.org/10.1055/s-2004-834894
Publikováno v:
The Journal of Organic Chemistry. 68:9166-9169
Two experimentally facile methods for the preparation of discrete oligoethers are reported. The first involves an iterative sequence of oxidation, acetal formation, and reductive ring opening for the synthesis of penta-1,4-butylene glycol. The second
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acb0717d1e62cff1f8de30fa75953b89
https://doi.org/10.1021/jo034728k
https://doi.org/10.1021/jo034728k
Autor:
Parag V. Jog, Mary S. Gin
Publikováno v:
Organic letters. 10(17)
A gated synthetic ion channel with beta-cyclodextrin as the pore and azobenzene as the gate is reported. Irradiation converts a tethered trans-azobenzene to cis-azobenzene which likely transforms the channel from a self-inclusion complex to a dissoci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::249516b8396329ea0a5a48f4d2e33e6b
https://pubmed.ncbi.nlm.nih.gov/18656946
https://pubmed.ncbi.nlm.nih.gov/18656946
Publikováno v:
Nanobiotechnology II: More Concepts and Applications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef43cebf757560f596e0c6b2a3e0767b
https://doi.org/10.1002/9783527610389.ch1
https://doi.org/10.1002/9783527610389.ch1
Publikováno v:
ChemInform. 37
A highly convergent strategy for the synthesis of C3- or C2-symmetric oligosaccharide macrocycles is reported. Molecular modeling indicates these macrocycles possess sterically congested cavities. Weak host−guest interactions are observed that shou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::422008946ac82cd2fd7f23930c504108
https://doi.org/10.1002/chin.200603186
https://doi.org/10.1002/chin.200603186
Publikováno v:
Organic letters. 7(20)
[structure: see text] A highly convergent strategy for the synthesis of C3- or C2-symmetric oligosaccharide macrocycles is reported. Molecular modeling indicates these macrocycles possess sterically congested cavities. Weak host-guest interactions ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c009db39c1555ecd6dae23f356f8b55
https://pubmed.ncbi.nlm.nih.gov/16178563
https://pubmed.ncbi.nlm.nih.gov/16178563
Publikováno v:
ChemInform. 36
A new iterative route to substituted acenes is reported that centers on regioselective cycloaddition of a nickel-benzyne and 1-trimethylsilyl-1,3-pentadiyne. The five-step sequence installs two fused aromatic rings and two methyl substituents onto th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dd678e7d07b8ad1efec98e75538b599
https://doi.org/10.1002/chin.200520094
https://doi.org/10.1002/chin.200520094