Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Aranorosin"'
Publikováno v:
Tetrahedron. 91:132240
Penicimutans and aranorosins are a rich family of secondary metabolites produced by fungi of terrestrial and marine origin. These natural products contain polyketides, indole alkloids or both. The aranorosin-type polyketides feature an unusually hexa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cabcdcf50881d2624597b1f98f3b6234
https://doi.org/10.1016/j.tet.2021.132240
https://doi.org/10.1016/j.tet.2021.132240
Publikováno v:
Tetrahedron Letters. 34:5519-5522
A short synthesis of the novel antibiotic aranorosin is described which employs a novel hypervalent iodine-mediated oxidative hydroxylation of a tyrosinal derivative in the key step. A similar procedure was employed to prepare 6′-epiaranorosin, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05ada101fd85f62b655885904b542025
https://doi.org/10.1016/s0040-4039(00)73870-6
https://doi.org/10.1016/s0040-4039(00)73870-6
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bcc58ea2b05295d9cccd1222b145900
https://doi.org/10.1002/chin.199306109
https://doi.org/10.1002/chin.199306109
Autor:
Peter Wipf, Yuntae Kim
Publikováno v:
ChemInform. 24
Oxidative cyclization of L-tyrosine, stereoselective addition of an α-alkoxy organolithium reagent, and hydroxyl-directed diepoxidation are key steps in the first synthesis of the fully functionalized core of aranorsin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eeae5b7bcc23d5a5074bb4b600abf6be
https://doi.org/10.1002/chin.199331160
https://doi.org/10.1002/chin.199331160
Publikováno v:
ChemInform. 24
A short synthesis of the novel antibiotic aranorosin is described which employs a novel hypervalent iodine-mediated oxidative hydroxylation of a tyrosinal derivative in the key step. A similar procedure was employed to prepare 6′-epiaranorosin, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::988110c199169d740a4296ca139564ea
https://doi.org/10.1002/chin.199352292
https://doi.org/10.1002/chin.199352292
Autor:
E. K. S. Vijayakumar, B. N. Ganguli, Triptikumar Mukhopadhyay, R. G. Bhat, Kirity Roy, Sugata Chatterjee
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b87ad0432bcca805e11ea4ff127f8d09
https://doi.org/10.1002/chin.199843272
https://doi.org/10.1002/chin.199843272
Publikováno v:
Tetrahedron Letters. 32:6613-6616
Protocols that led to the construction of cyclohexanone bisoxirane as a part of l-oxaspiro[4,5]decane moiety present in aranorosin, are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cb41b88241dda5ad51a68c57f2d1fa7
https://doi.org/10.1016/0040-4039(91)80236-y
https://doi.org/10.1016/0040-4039(91)80236-y
Autor:
R. G. Bhat, Kirity Roy, E. K. S. Vijayakumar, Sugata Chatterjee, Triptikumar Mukhopadhyay, B. N. Ganguli
Publikováno v:
The Journal of Antibiotics. 51:522-524
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edc8c64fef9e624d8c83df11ff303b2e
https://doi.org/10.7164/antibiotics.51.522
https://doi.org/10.7164/antibiotics.51.522
Publikováno v:
Synlett. 1992:201-203
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3fba41dd46d77fa147e0030f37a9c97
https://doi.org/10.1055/s-1992-21313
https://doi.org/10.1055/s-1992-21313
Publikováno v:
Synlett. 1992:1005-1006
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::648488f585e37862fcc0ede2a01fde4c
https://doi.org/10.1055/s-1992-21564
https://doi.org/10.1055/s-1992-21564