Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Keishi Funaki"'
Autor:
Yukihiro Sagawa, Makoto Urahata, Hiroya Sasahara, Kozo Hori, Yumiko Shibata, Kei Takeda, Eiichi Yoshii, Keishi Funaki
Publikováno v:
The Journal of Organic Chemistry. 50:4673-4681
Synthese de l'[hydroxy-3' methyl-2' propenyl]-10 methoxy-4 oxa-1spiro [4.5] decadiene-3,7one-2 (A) et de son derive methoxymethoxymethyl-7 a partir respectivement du tetrahydro-3a,4,7,7a phtalide et de l'hexadiene-2,4diol-1,6. A est couple avec l'[hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6398c99765470447007bf9575fccd26a
https://doi.org/10.1021/jo00224a002
https://doi.org/10.1021/jo00224a002
Publikováno v:
Tetrahedron Letters. 23:3069-3072
Synthesis of methyl α-D-tetronitroside( 11 ) from D-mannose via methyl α-D-mycaroside( 1 ) established the D-configuration for tetronitrose(kijanose), a novel nitro sugar which occurs as a component of the antitumor antibiotics tetrocarcins A an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b53162850be22e12abb3743f68282b3
https://doi.org/10.1016/s0040-4039(00)87535-8
https://doi.org/10.1016/s0040-4039(00)87535-8
Publikováno v:
Chemical and Pharmaceutical Bulletin. 30:4031-4036
Methyl α-and β-DL-2, 3, 4, 6-tetradeoxy-4-(methoxycarbonylamino)-3-C-methyl-3-nitro-xylo-hexopyranosides (13a, b) were synthesized from methyl α-and β-DL-2, 3, 4, 6-tetradeoxy-hex-3-enopyranosides (2). The key step in the syntheses involved regio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65d3d57c4e738e3a218cce8a0d5de1c8
https://doi.org/10.1248/cpb.30.4031
https://doi.org/10.1248/cpb.30.4031
Publikováno v:
Chemischer Informationsdienst. 14
Methyl α-and β-DL-2, 3, 4, 6-tetradeoxy-4-(methoxycarbonylamino)-3-C-methyl-3-nitro-xylo-hexopyranosides (13a, b) were synthesized from methyl α-and β-DL-2, 3, 4, 6-tetradeoxy-hex-3-enopyranosides (2). The key step in the syntheses involved regio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a48377a5dd39d4e395e16ba837b9ab47
https://doi.org/10.1002/chin.198327218
https://doi.org/10.1002/chin.198327218