Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Flavolipin"'
Publikováno v:
Journal of Endotoxin Research. 2003, Vol. 9 Issue 5, p301-307. 7p.
Publikováno v:
Tetrahedron. 54:15701-15710
Topostins B567 (2b) and D654 (3b) (WB-3559D, flavolipin) have been efficiently synthesized from 1, 10-decanediol (5) in 11 and 13 steps, respectively, involving an asymmetric hydrogenation of the β-keto ester14 using(R)-BINAP ruthenium bromide and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e65fe37f8ecf230fcf504b521685f1d0
https://doi.org/10.1016/s0040-4020(98)00984-3
https://doi.org/10.1016/s0040-4020(98)00984-3
Autor:
Yohko Kawai, Noriko Deguchi, Hideyuki Haruyama, Masahiro Nishijima, Masao Shiozaki, Tomio Ishikawa
Publikováno v:
Tetrahedron Letters. 39:4497-4500
The proposed structure of natural flavolipin was revised as N-[N-[(3R)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl]-L-serine as a result of synthetic study and biological activity test.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::701d68d9e9c3d4fc5643b9c7776f7567
https://doi.org/10.1016/s0040-4039(98)00798-9
https://doi.org/10.1016/s0040-4039(98)00798-9
Publikováno v:
ChemInform. 27
All four stereoisomers of flavolipin were synthesized from d -glucose in a stereocontrolled manner. None of them was identical with the reported natural product.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03451818d90507dcb008f092fea9dd80
https://doi.org/10.1002/chin.199638234
https://doi.org/10.1002/chin.199638234
Autor:
Noriko Deguchi, Yohko Kawai, Masao Shiozaki, Hideyuki Haruyama, Tomio Ishikawa, Masahiro Nishijima
Publikováno v:
ChemInform. 29
The proposed structure of natural flavolipin was revised as N-[N-[(3R)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl]-L-serine as a result of synthetic study and biological activity test.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c4e69e88e0acdd847055e7aa849d3d5
https://doi.org/10.1002/chin.199836277
https://doi.org/10.1002/chin.199836277
Autor:
Masahiro Nishijima, Noriko Deguchi, Masao Shiozaki, Yohko Kawai, Tomio Ishikawa, Hideyuki Haruyama, Takashi Mochizuki, Takanori Wakabayashi
Publikováno v:
ChemInform. 30
The proposed structure of natural flavolipin was revised as N-[N-[(3R)-15-methyl-3- (13-methyltetradecanoyloxy)hexadecanoyl]glycyl]-L-serine as a result of a synthetic study and biological activity tests, and its isomers were synthesized in a stereoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7367d39f26b58a1003218d484f1ecc6d
https://doi.org/10.1002/chin.199902245
https://doi.org/10.1002/chin.199902245
Publikováno v:
ChemInform. 30
Topostins B567 (2b) and D654 (3b) (WB-3559D, flavolipin) have been efficiently synthesized from 1, 10-decanediol (5) in 11 and 13 steps, respectively, involving an asymmetric hydrogenation of the β-keto ester14 using(R)-BINAP ruthenium bromide and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58976e441a8caf9950261a79029cb047
https://doi.org/10.1002/chin.199918223
https://doi.org/10.1002/chin.199918223
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