Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Junji Yoshizawa"'
Autor:
Junji Yoshizawa
Publikováno v:
Japanese Journal of Pharmacoepidemiology/Yakuzai ekigaku. 4:105-111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ca328238de2c465c8c146d7ec25c99f
https://doi.org/10.3820/jjpe1996.4.105
https://doi.org/10.3820/jjpe1996.4.105
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05b958f8c1a57069f7fa70a728514ff2
https://doi.org/10.1002/chin.199413070
https://doi.org/10.1002/chin.199413070
Autor:
Akira Hosomi, Jun-ichi Tateiwa, Shin-ya Nakamura, Yoshihiro Funahashi, Makoto Hojo, Junji Yoshizawa, Ryo Okada
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa30437459757cded569dc9d990389b3
https://doi.org/10.1002/chin.199924144
https://doi.org/10.1002/chin.199924144
Publikováno v:
The Journal of Organic Chemistry. 58:6541-6542
Reduction of ketene dithioacetals by samarium iodides was studied. Stereochemical synthesis of organic sulfur compounds was observed via a samarium complex. 2 tabs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1aac0d206f8ba3cfec8a3980ed78e2bb
https://doi.org/10.1021/jo00076a004
https://doi.org/10.1021/jo00076a004
Autor:
Jun-ichi Tateiwa, Shin-ya Nakamura, Yoshihiro Funahashi, Akira Hosomi, Makoto Hojo, Junji Yoshizawa, Ryo Okada
Publikováno v:
HETEROCYCLES. 49:85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d452b5ef755ef235a79bec272072922
https://doi.org/10.3987/com-98-s37
https://doi.org/10.3987/com-98-s37
Publikováno v:
The Journal of Antibiotics. 35:1500-1506
Forphenicinol, L-2-(3-hydroxy-4-hydroxymethylphenyl)glycine, was synthesized by two methods starting from dimethyl hydroxyterephthalate or DL-2-(3-hydroxyphenyl)glycine. Forphenicine, L-2-(4-formyl-3-hydroxyphenyl)glycine, was prepared from L-forphen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1a0efa4b55299c9c0f69374788c0900
https://doi.org/10.7164/antibiotics.35.1500
https://doi.org/10.7164/antibiotics.35.1500
Publikováno v:
JOURNAL OF CHEMICAL ENGINEERING OF JAPAN. 5:361-364
A fully developed turbulent flow of an electrolyte solution in a porous-wall tube with suction or injection flow through the wall was experimentally studied. The measurements of mass transfer rates at the wall were made by an electrochemical method.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4da75eabace4c4f9f48441374185fd7
https://doi.org/10.1252/jcej.5.361
https://doi.org/10.1252/jcej.5.361
Autor:
Junji Yoshizawa, Munemitsu Tomoeda
Publikováno v:
Tetrahedron Letters. 8:975-979
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da1a6a3b70e93fbc5223ce2fce178cbe
https://doi.org/10.1016/s0040-4039(00)90619-1
https://doi.org/10.1016/s0040-4039(00)90619-1
Publikováno v:
Chemical and Pharmaceutical Bulletin. 15:845-853
Pyrolytic cleavage of the azo-bridge of diethyl azodicarboxylate (Ia) at 200∼210° was studied and was shown to give diethyl oxalate (VI), tetraethyl hydrazine-N1, N1, N2, N2-tetra-carboxylate (VIII), triethyl hydrazine-N1, N1, N2-tricarboxylate (I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44c1229fcb5fb8ffbe99d13923fe2284
https://doi.org/10.1248/cpb.15.845
https://doi.org/10.1248/cpb.15.845
Autor:
Junji Yoshizawa, Munemitsu Tomoeda
Publikováno v:
J. Chem. Soc. C. :1741-1747
Diethyl azodicarboxylate (I) reacts readily with 3β-benzoyloxy-20-acetoxypregna-5,16,20-triene (V) affording in high yield two isomeric Diels–Alder adducts differing only in their stereochemistry at C(16), 16α-(VIa)(major product) and 16β-(VIb)(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9732b62d34b03608711f6e9ff8d8917f
https://doi.org/10.1039/j39710001741
https://doi.org/10.1039/j39710001741