Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Mitsutaka. Kawazu"'
Autor:
B. R. Baker, Mitsutaka. Kawazu
Publikováno v:
Journal of medicinal chemistry. 10(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6eba98ff7eda1b666e712c2489065c3
https://pubmed.ncbi.nlm.nih.gov/22185121
https://pubmed.ncbi.nlm.nih.gov/22185121
Autor:
Mitsutaka. Kawazu, B. R. Baker
Publikováno v:
Journal of medicinal chemistry. 10(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ca5aaba5da4b67092a3061d98001bed
https://pubmed.ncbi.nlm.nih.gov/22185122
https://pubmed.ncbi.nlm.nih.gov/22185122
Autor:
Takeshi Kanno, Mitsutaka. Kawazu
Publikováno v:
Chemical and Pharmaceutical Bulletin. 22:2851-2860
Reaction of 5-O-tosyl-3-benzyloxycarbonylamido-3-deoxy-1, 2-O-isopropylidene-α-D-ribofuranose (21) or 5-O-tosyl-3-acetamido-3-deoxy-1, 2-O-isopropylidene-α-D-ribofuranose (30) with the sodium salt of adenine afforded the corresponding isomeric "rev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a87ced35dfc31e5c49a5e93a9fffddf4
https://doi.org/10.1248/cpb.22.2851
https://doi.org/10.1248/cpb.22.2851
Autor:
Mitsutaka. Kawazu, Takeshi Kanno
Publikováno v:
Chemical and Pharmaceutical Bulletin. 22:2836-2850
Reaction of methyl 5-O-tosyl-2, 3-O-isopropylidene-β-D-ribofuranoside (1) with the sodium salts of purines, (2) and (3), and pyrimidines, (12), (13), and (14) derivatives in DMF afforded the corresponding "reversed nucleosides". 6-Alkylaminopurine a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0971f6d65536acb1bb626119de6fd18f
https://doi.org/10.1248/cpb.22.2836
https://doi.org/10.1248/cpb.22.2836
Autor:
Kentaro Okumura, Toyonari Oine, Yoshihisa Yamada, Masayasu Tomie, Takeshi Adachi, Takeo Nagura, Mitsutaka Kawazu, Tomishige Mizoguchi, Ichizo Inoue
Publikováno v:
The Journal of Organic Chemistry. 36:1573-1579
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e6551941199e774a105162c89f7b1f4
https://doi.org/10.1021/jo00811a001
https://doi.org/10.1021/jo00811a001
Autor:
Mitsutaka Kawazu
Publikováno v:
YAKUGAKU ZASSHI. 78:399-402
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e27f564c32a22fcd627c8df4e5b42f8
https://doi.org/10.1248/yakushi1947.78.4_399
https://doi.org/10.1248/yakushi1947.78.4_399
Publikováno v:
YAKUGAKU ZASSHI. 79:1184-1187
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::475eb865f14699e048a01f9051776a9c
https://doi.org/10.1248/yakushi1947.79.9_1184
https://doi.org/10.1248/yakushi1947.79.9_1184
Autor:
Mitsutaka Kawazu
Publikováno v:
YAKUGAKU ZASSHI. 78:402-406
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adf03f3e7a4d40ccdddd33bd26fe07c9
https://doi.org/10.1248/yakushi1947.78.4_402
https://doi.org/10.1248/yakushi1947.78.4_402
Autor:
M. Fujihara, Mitsutaka Kawazu
Publikováno v:
Chemical and Pharmaceutical Bulletin. 20:88-92
Treatment of 4-aminobenzofuran derivatives with hydrochloric acid led to the formation of 4-hydroxyindole derivatives in good yields, wheras alkaline hydrolysis of 4-acylaminobenzofurans gave 4-aminobenzofurans normally. Synthesis of pyrrolocoumarins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83b92c311a19993482f418d2cd77d153
https://doi.org/10.1248/cpb.20.88
https://doi.org/10.1248/cpb.20.88
Publikováno v:
The Journal of Organic Chemistry. 38:2891-2895
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0a25e806452768ceab28e489a86bcab
https://doi.org/10.1021/jo00956a034
https://doi.org/10.1021/jo00956a034