Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Katherine Buggle"'
Publikováno v:
Monatshefte f�r Chemie Chemical Monthly. :945-951
The conversion of 2H-[1]benzothieno[3,2-b]pyran-2-ones into mono- and dithio-derivatives and the preparation of some dibenzothiophenes, sulphines and pyridones are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71fc0d3d65e9dbfcb9479be38b6d1552
https://doi.org/10.1007/bf00810104
https://doi.org/10.1007/bf00810104
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 113:81-90
2-(1H-Heteroarylidene)-1H-indene-1,3(2H)-diones were converted into anils and dianils and then into monothio- and dithio-derivatives by treatment with hydrogen sulphide. The 2-pyridinyl monothioderivate was converted into S-alkyl ethers. In contrast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::684d564e7cbc3afc317114de80fe86cc
https://doi.org/10.1007/bf00814340
https://doi.org/10.1007/bf00814340
Publikováno v:
The Irish Journal of Medical Science. 35:345-352
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2828dfb9fa2545ee9d87fa5b6cc0a39
https://doi.org/10.1007/bf02945619
https://doi.org/10.1007/bf02945619
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1427-1429
The title compound (3a) was prepared by the reaction of 2-benzoylbenzo[b]thiophen-3(2H)-one 1,1-dioxide (1) with tetraphosphorus decasulphide, acetonitrile, and sodium hydrogen carbonate. The structure was confirmed by an alternative synthesis from e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0703e7bb22b6f1cf8fc47c32a8999f1d
https://doi.org/10.1039/p19830001427
https://doi.org/10.1039/p19830001427
Autor:
Katherine Buggle, Bernadette Fallon
Publikováno v:
Monatshefte f�r Chemie Chemical Monthly. 118:1197-1199
Benzothiopyran-2 and 4-thiones and benzopyran-2-thiones undergo oxidation to sulphines which on further oxidation give the carbonyl derivatives or polymeric products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c0e0717c499afa14b9a584d1aef9019
https://doi.org/10.1007/bf00811293
https://doi.org/10.1007/bf00811293
Autor:
KATHERINE BUGGLE, DANIEL O'SULLIVAN
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37d964f845b52fe193b4867aae2cf814
https://doi.org/10.1002/chin.197625220
https://doi.org/10.1002/chin.197625220
Autor:
KATHERINE BUGGLE, DANIEL O'SULLIVAN
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa3d71ef39f382b4c292be490c1af403
https://doi.org/10.1002/chin.197524143
https://doi.org/10.1002/chin.197524143
Autor:
Katherine Buggle, Bernadette Fallon
Publikováno v:
ChemInform. 19
Benzothiopyran-2 and 4-thiones and benzopyran-2-thiones undergo oxidation to sulphines which on further oxidation give the carbonyl derivatives or polymeric products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2d6c0df179729a2085228a805fe9c0b
https://doi.org/10.1002/chin.198806111
https://doi.org/10.1002/chin.198806111
Publikováno v:
Chemischer Informationsdienst. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::382e0f8339243998b412371356b74735
https://doi.org/10.1002/chin.197330257
https://doi.org/10.1002/chin.197330257
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2075-2076
3,4-Disubstituted 1-naphthols (5a–h) are obtained in 49–89% yield by the reaction of 2,3-disubstituted inden-1-ones (1a–h) with lithium methylsulphinylmethanide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3173f0717260860053d5ed368bcaeea4
https://doi.org/10.1039/p19830002075
https://doi.org/10.1039/p19830002075