Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Seitaro Saeki"'
Autor:
Seitaro Saeki
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48c274a1844cf959b89db7ee6874e56c
https://doi.org/10.1002/chin.199235313
https://doi.org/10.1002/chin.199235313
Autor:
Seitaro Saeki
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 50:213-224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31e22ff8c598f5212898a548c078e99a
https://doi.org/10.5059/yukigoseikyokaishi.50.213
https://doi.org/10.5059/yukigoseikyokaishi.50.213
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b56e2d4a450d42b54501a0ff49f9f60e
https://doi.org/10.1002/chin.199016111
https://doi.org/10.1002/chin.199016111
Publikováno v:
Chemical and Pharmaceutical Bulletin. 28:424-430
Chinolin-N-oxid (I) reagiert mit Tosylchlorid (II) in Gegenwart von Triethylamin hauptsachlich zum Dichinolylether (IV) und dem Chinolyllactam (V) neben dem Tosylat (III) und dem Lactam (VI).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86993a7e27fff944afd5a39b97503762
https://doi.org/10.1248/cpb.28.424
https://doi.org/10.1248/cpb.28.424
Publikováno v:
Chemical and Pharmaceutical Bulletin. 29:1827-1831
1-Hydroxy-2-phenylindole (1) reacts with tosyl chloride and p-nitrobenzenesulfonyl chloride in DMF-pyridine to give the corresponding 2-phenyl-3-sulfonyloxyindole (2 and 4). Benzoyl chloride is less reactive, and 1-benzoyloxy-2-phenylindole (5) or 3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a0206b2f29e5a09fc51af2fd5f9095d
https://doi.org/10.1248/cpb.29.1827
https://doi.org/10.1248/cpb.29.1827
Publikováno v:
Chemical and Pharmaceutical Bulletin. 24:2509-2516
In order to introduce 2-pyridyl group into the 9 position of 1, 1-disubstituted quinolizidine, N-benzoyloxypyridinium chloride (1) was treated with 9-dehydro-1-oxoquinolizidine (3), dehydro-1-ethoxycarbonyl-1-hydroxyquinolizidine (13) and 9-dehydro-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7177983c1a84b55935223a0953ee2f3a
https://doi.org/10.1248/cpb.24.2509
https://doi.org/10.1248/cpb.24.2509
Publikováno v:
Chemical and Pharmaceutical Bulletin. 34:4629-4634
This paper describes a conversion of (-)-limonen-10-ol to the key intermediate (1) for 11-deoxyprostaglandin. The 3, 4-cis-disubstituted cyclopentanone (2), which was easily obtained from (-)-limonen-10-ol in a stereocontrolled fashion by means of Rh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6967f0f10cc585bf1958eee6c8098f1e
https://doi.org/10.1248/cpb.34.4629
https://doi.org/10.1248/cpb.34.4629
Publikováno v:
Chemical and Pharmaceutical Bulletin. 32:2154-2159
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d4548be626c1095c1c5dc55d798d437
https://doi.org/10.1248/cpb.32.2154
https://doi.org/10.1248/cpb.32.2154
Publikováno v:
Chemical and Pharmaceutical Bulletin. 22:2341-2345
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66bd2ed2abd30c69f95613f6fbe985a8
https://doi.org/10.1248/cpb.22.2341
https://doi.org/10.1248/cpb.22.2341
Publikováno v:
Chemical and Pharmaceutical Bulletin. 33:4021-4025
The conversion of naturally abundant (+)-limonen-10-ol (2) into the synthetic intermediate (3) for brefeldin A is described. The cis-3, 4-disubstituted cyclopentanone (4), which was easily obtained from 2 by Rh (I)-catalyzed cyclization reaction via
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0291bc3b177c194ea35b4f30f8fae3e
https://doi.org/10.1248/cpb.33.4021
https://doi.org/10.1248/cpb.33.4021