Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hishani Prabaharan"'
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :379-389
The syntheses of bis-spiroacetals 25a, 25c and 40 which constitute the central framework of the polyether antibiotic CP44,161 4, are described. The tricyclic bis-spiroacetal ring is formed by oxidative cyclisation of hydroxyspiroacetal 9 which in tur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f639d490b1d6ac14fb1cd1aba953c71
https://doi.org/10.1039/b008159k
https://doi.org/10.1039/b008159k
Publikováno v:
Tetrahedron. 56:1937-1992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5de889da27b534b4b80e0aae64f9df5d
https://doi.org/10.1016/s0040-4020(99)01021-2
https://doi.org/10.1016/s0040-4020(99)01021-2
Publikováno v:
Synlett. 1999:295-298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1264ac3d01ac8c7f8fd3ab95bd014574
https://doi.org/10.1055/s-1999-2607
https://doi.org/10.1055/s-1999-2607
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2795-2801
The synthesis of tetracyclic polyethers 16 and 17, which are closely related to the polyether antibiotics epi-17-deoxy-(O-8)-salinomycin 3 and CP44,161 4, is described. The key step involved Barbier–Grignard addition of bromide 8 to bis-spiroacetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6712a56d4f92c84dc0e37cad2c55cc54
https://doi.org/10.1039/a905339e
https://doi.org/10.1039/a905339e
Publikováno v:
Tetrahedron. 54:2113-2128
The work described herein provides a model system for appendage of the E ring of epi-17-deoxy-(O-8)-salinomycin3 onto bis-spiroacetal aldehyde 6. The conversion of aldehyde 7 to bicyclic ether 8 via silver assisted ring expansion of the mesylate deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a0b9950c82666ba607457fb338c13b4
https://doi.org/10.1016/s0040-4020(97)10420-3
https://doi.org/10.1016/s0040-4020(97)10420-3
Publikováno v:
ChemInform. 27
The first syntheses of the pyranonaphthoquinone antibiotics 5-epi-arizonin B1 16, 5-epi-arizonin C1 15 and arizonin C1 3 are described. The key steps involve addition of 2-trimethylsilyloxyfuran 12 to the 2-acetylnaphthoquinone 11 affording the adduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53996354bf4d350cd67eec49cf3a10b8
https://doi.org/10.1002/chin.199610310
https://doi.org/10.1002/chin.199610310
Publikováno v:
ChemInform. 28
The preparation of 8-bromokalafungin (20) which is a key intermediate for the synthesis of C-glycoside containing pyranonaphthoquinone antibiotics related to medermycin (6) is described. Although attempts to selectively monobrominate kalafungin (1) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02a661a63368c9181a9781b570a739dc
https://doi.org/10.1002/chin.199751276
https://doi.org/10.1002/chin.199751276
Publikováno v:
ChemInform. 31
The synthesis of tetracyclic polyethers 16 and 17, which are closely related to the polyether antibiotics epi-17-deoxy-(O-8)-salinomycin 3 and CP44,161 4, is described. The key step involved Barbier–Grignard addition of bromide 8 to bis-spiroacetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2868302c5d92299f106e32c251d7fb4c
https://doi.org/10.1002/chin.200004250
https://doi.org/10.1002/chin.200004250
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6188c809f78aae154807264699093146
https://doi.org/10.1002/chin.200027256
https://doi.org/10.1002/chin.200027256
Publikováno v:
ChemInform. 32
The syntheses of bis-spiroacetals 25a, 25c and 40 which constitute the central framework of the polyether antibiotic CP44,161 4, are described. The tricyclic bis-spiroacetal ring is formed by oxidative cyclisation of hydroxyspiroacetal 9 which in tur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ab3fc2b8264d02dc6874d8b24ea8edd
https://doi.org/10.1002/chin.200130226
https://doi.org/10.1002/chin.200130226