Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nicholas M. Hext"'
Autor:
Nicholas M. Hext, Mark Mascal, Johan P. Turkenburg, James R. Arnall-Culliford, Ralf Warmuth, Madeleine H. Moore
Publikováno v:
The Journal of Organic Chemistry. 64:8479-8484
The guanine−cytosine base hybrid 1 is synthesized in five steps from the malononitrile dimer. One face of the molecule possesses the cytosine AAD hydrogen bonding code and the other the guanine DDA...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b711b22357a626783496b83a7939bc
https://doi.org/10.1021/jo990719t
https://doi.org/10.1021/jo990719t
Publikováno v:
Pure and Applied Chemistry. 70:2371-2377
An approach to the design of artificial receptors is described involving the fusion of several sixmembered rings, preorganizing nitrogen and oxygen hydrogen bonding sites. A hexagonal lattice chemosensor extracts the blood metabolite creatinine into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc21c01925d9e6e7a16d5adcf86c3fb9
https://doi.org/10.1351/pac199870122371
https://doi.org/10.1351/pac199870122371
Publikováno v:
Helvetica Chimica Acta. 81:1749-1753
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b1aa5ead88a93fd0058757d22091d3c
https://doi.org/10.1002/(sici)1522-2675(19981007)81:10<1749::aid-hlca1749>3.0.co
https://doi.org/10.1002/(sici)1522-2675(19981007)81:10<1749::aid-hlca1749>3.0.co
Autor:
David E. Hibbs, Oleg V. Shishkin, Mark Mascal, Alexander J. Blake, Michael B. Hursthouse, J. Hansen, Nicholas M. Hext
Publikováno v:
The Journal of Organic Chemistry. 63:6016-6020
Azatriquinane, a tricyclic amine with rigid, hemispherical topology, is synthesized in six steps from pyrrole. This first example of a [2.2.2]cyclazine can be oxidatively dimerized to a novel, highly strained heptacycle or oxidized with chlorine to g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ab13b19b9d8f952f90b60526ffe5090
https://doi.org/10.1021/jo980788s
https://doi.org/10.1021/jo980788s
Publikováno v:
Tetrahedron Letters. 37:131-134
Azatriquinane, an amine with a rigid, hemispherical topology, is synthesized in six steps from pyrrole. It is shown to be more basic than quinuclidine, and can be dimerized by N-oxidation and treatment with base to give novel, highly strained heptacy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7844aaf42d4ebf1e2c8c525a3e976ddf
https://doi.org/10.1016/0040-4039(95)02091-8
https://doi.org/10.1016/0040-4039(95)02091-8
Autor:
Roger W. Alder, Alex R. Thomas, Kevin S. Turner, Martin H. Perry, Paul R. Allen, Paul M. Gore, Lee S. Edwards, Gordon I. Fray, Nicholas M. Hext, Katy E. Fuller
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :3071-3077
A synthetic strategy for the preparation of chains of 1,2:4,5-fused cyclohexa-1,4-diene rings, both linear and cyclic (beltenes), based on the repetitive Diets-Alder cycloaddition of p-benzoquinone with a tetramethylene-ethane synthon (3,4-dimethylen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::012954de7a97db4c2099791efc3a5587
https://doi.org/10.1039/p19940003071
https://doi.org/10.1039/p19940003071
Autor:
Paul R. Allen, Nicholas M. Hext, Kevin S. Turner, Roger W. Alder, Alex R. Thomas, Gordon I. Fray, Lee S. Edwards, Katy E. Fuller, Martin H. Perry, Paul M. Gore
Publikováno v:
ChemInform. 26
A synthetic strategy for the preparation of chains of 1,2:4,5-fused cyclohexa-1,4-diene rings, both linear and cyclic (beltenes), based on the repetitive Diets-Alder cycloaddition of p-benzoquinone with a tetramethylene-ethane synthon (3,4-dimethylen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13ca296e8a7e024428715f3a48a11c4e
https://doi.org/10.1002/chin.199515146
https://doi.org/10.1002/chin.199515146
Publikováno v:
ChemInform. 27
Azatriquinane, an amine with a rigid, hemispherical topology, is synthesized in six steps from pyrrole. It is shown to be more basic than quinuclidine, and can be dimerized by N-oxidation and treatment with base to give novel, highly strained heptacy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9363adb973a708f7e8c079d1634abb4
https://doi.org/10.1002/chin.199618124
https://doi.org/10.1002/chin.199618124
Autor:
David E. Hibbs, Oleg V. Shishkin, Alexander J. Blake, Mark Mascal, Nicholas M. Hext, Michael B. Hursthouse, J. Hansen
Publikováno v:
ChemInform. 30
Azatriquinane, a tricyclic amine with rigid, hemispherical topology, is synthesized in six steps from pyrrole. This first example of a [2.2.2]cyclazine can be oxidatively dimerized to a novel, highly strained heptacycle or oxidized with chlorine to g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44883fdee69c7dca29a990f50fe89503
https://doi.org/10.1002/chin.199903130
https://doi.org/10.1002/chin.199903130
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65369fdd5017132cd80b2e5a1991fb01
https://doi.org/10.1002/chin.199852037
https://doi.org/10.1002/chin.199852037