Zobrazeno 1 - 7
of 7
pro vyhledávání: '"T. I. Martin"'
Publikováno v:
Canadian Journal of Chemistry. 52:2705-2713
Thionupharoline has been shown to be identical with 6-hydroxythiobinupharidine. The hydride reduction of hemiaminals of thiobinupharidine has been examined in ethanol solution. The steric course of reduction at C-6 is not nearly as selective as it ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8ce5d745516db7b9e471dbc20e9a478
https://doi.org/10.1139/v74-394
https://doi.org/10.1139/v74-394
Autor:
Chunfook Wong, David B. MacLean, Jerzy T. Wróbel, A. I-M. Tsai, J. Ruszkowska, K. Kabzinska, R. T. LaLonde, T. I. Martin
Publikováno v:
Canadian Journal of Chemistry. 54:3860-3868
The sulfoxide configurations of neothiobinupharidine α- and β-sulfoxides have been determined through a 13C nmr investigation. The 13C nmr sulfoxidation increments (ΔδC-i = δC–iS–O − δC–iS) for all carbons in 2,2,4,4-tetramethylthiolane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97ed0364b1d76edc9e4d352ce8c28aca
https://doi.org/10.1139/v76-555
https://doi.org/10.1139/v76-555
Publikováno v:
Canadian Journal of Chemistry. 51:2810-2820
The spectroscopic properties of thiobinupharidine and its isomer, neothiobinupharidine, of established structure, have been examined and compared. From this study it was possible to deduce the structure and relative configuration of the alkaloid. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ac4d154abff0c1cd45c00cc2c12ee30
https://doi.org/10.1139/v73-422
https://doi.org/10.1139/v73-422
Publikováno v:
Canadian Journal of Chemistry. 50:1831-1837
A new alkaloid, nupharolutine, (C15H23NO2) has been isolated from the basic extract of the rhizomes of Nupharluteum. By spectroscopic and chemical methods it is shown to be a hydroxy derivative of deoxynupharidine. The mass spectra of the new base an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc4a749d90fb59da7cae31bda0902bc9
https://doi.org/10.1139/v72-294
https://doi.org/10.1139/v72-294
Autor:
David B. MacLean, J. Poplawski, A. Iwanow, Jerzy T. Wróbel, Jerzy Szychowski, C. K. Yu, T. I. Martin
Publikováno v:
Canadian Journal of Chemistry. 50:1968-1971
A new alkaloid (C30H42N2O3S), isolated from Nupharluteum, is shown to be neothiobinupharidine sulfoxide. The mass spectra of neothiobinupharidine and the new alkaloid are discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f07449e685267914f38c800c2d478aca
https://doi.org/10.1139/v72-314
https://doi.org/10.1139/v72-314
Publikováno v:
Chemischer Informationsdienst. 5
Thionupharoline has been shown to be identical with 6-hydroxythiobinupharidine. The hydride reduction of hemiaminals of thiobinupharidine has been examined in ethanol solution. The steric course of...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48a48aac7e318f4ce13c512bd82a7cf7
https://doi.org/10.1002/chin.197444160
https://doi.org/10.1002/chin.197444160
Autor:
J. Poplawski, David B. MacLean, T. I. Martin, J. Szychowski, C. K. Yu, Jerzy T. Wróbel, C. Braekman-Danheux, A. Iwanow
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25a9ef48fb237ee3a2a032c2717fb69d
https://doi.org/10.1002/chin.197243446
https://doi.org/10.1002/chin.197243446