Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Daniel R. Carcanague"'
Autor:
Daniel R. Carcanague
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2805-2808
The synthesis of a new series of pseudomonic acid analogs is described. The synthetic approach is based on replacement of the C9C14 sidechain of the parent molecule with a modified amino substituent. The most potent member of the compound series c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5d3b60ee8e2ec29fe67e71ace1318cb
https://doi.org/10.1016/s0960-894x(97)10088-9
https://doi.org/10.1016/s0960-894x(97)10088-9
Publikováno v:
Synthetic Communications. 26:935-944
The asymmetric synthesis of multi-gram quantities of a pseudomonic acid precursor is described. Improvements on the literature synthesis of diacetyl arabinal from arabinose are also reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::388b748e5393cd17f94c9ead17abf717
https://doi.org/10.1080/00397919608003698
https://doi.org/10.1080/00397919608003698
Publikováno v:
Tetrahedron. 51:401-421
The synthesis, characterization, and steroid binding properties of two novel cyclophane receptors shaped by two naphthylphenylmethane spacers are reported. Cyclophane 1 forms inclusion complexes with bile acids, corticoids, and androgenic steroids in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f53b215c40a642e5d9e798c4e1beedda
https://doi.org/10.1016/0040-4020(94)00905-a
https://doi.org/10.1016/0040-4020(94)00905-a
Publikováno v:
Helvetica Chimica Acta. 77:800-818
New tricyclic spacers, readily available through fourfold Mannich reaction of substituted dibenzyl ketones, were introduced into a series of ten H2O-soluble cyclophanes with spacious preorganized cavity binding sites. These spacers provide H2O-solubi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8d2d738cf076a98eddf4f3839571c67
https://doi.org/10.1002/hlca.19940770320
https://doi.org/10.1002/hlca.19940770320
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d12f75bfa3b205da3e77b6ac79167b9a
https://doi.org/10.1002/chin.199223200
https://doi.org/10.1002/chin.199223200
Publikováno v:
ChemInform. 25
New tricyclic spacers, readily available through fourfold Mannich reaction of substituted dibenzyl ketones, were introduced into a series of ten H2O-soluble cyclophanes with spacious preorganized cavity binding sites. These spacers provide H2O-solubi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a241f9ff2b096a24e7ea5c1f4420fef0
https://doi.org/10.1002/chin.199436189
https://doi.org/10.1002/chin.199436189
Autor:
Daniel R. Carcanague
Publikováno v:
ChemInform. 29
The synthesis of a new series of pseudomonic acid analogs is described. The synthetic approach is based on replacement of the C9C14 sidechain of the parent molecule with a modified amino substituent. The most potent member of the compound series c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83f6f9dd456ca01d80bae9fda1e280bc
https://doi.org/10.1002/chin.199811260
https://doi.org/10.1002/chin.199811260
Autor:
Gunnar Svensson, Åke Oskarsson, Daniel R. Carcanague, Ito Chao, Jürgen Köhler, Arndt Simon, Kendall N. Houk, Bertil Norén
Publikováno v:
Acta Chemica Scandinavica. 46:244-248
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c030d80d5be515318cdc1fefe1c65fd
https://doi.org/10.3891/acta.chem.scand.46-0244
https://doi.org/10.3891/acta.chem.scand.46-0244
Autor:
István Banyai, Johan Blixt, Julius Glaser, Imre Tóth, Susan Jagner, Daniel R. Carcanague, Ito Chao, K. N. Houk
Publikováno v:
Acta Chemica Scandinavica. 46:138-141
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e68043b2e0e8b423d2f78679f8b13adf
https://doi.org/10.3891/acta.chem.scand.46-0138
https://doi.org/10.3891/acta.chem.scand.46-0138
Autor:
Diana Mondeshka, Ivanka Angelova, Birgitta Stensland, Per-Erik Werner, Chavdor Ivanov, Daniel R. Carcanague, Ito Chao, K. N. Houk
Publikováno v:
Acta Chemica Scandinavica. 46:54-59
Stereospecific multistep synthesis and resolution of 6,7-dimethoxy-4- phenyl-1,2,3,4-tetrahydroisoquinoline (3) has been achieved from its racemic base. The absolute configurations of the optical antipodes converted into their hydrochloride salt form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1730e2de57b4fae14ada543cb05d879
https://doi.org/10.3891/acta.chem.scand.46-0054
https://doi.org/10.3891/acta.chem.scand.46-0054