Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Stephen L. Birkett"'
Autor:
Tim Quach, Mark A. Rizzacasa, Bill C. Hawkins, Danny Ganame, Sebastien Meiries, Stephen L. Birkett
Publikováno v:
The Journal of Organic Chemistry. 78:116-123
The total synthesis of the proposed structure for the minor myxobacterial metabolite 8-deshydroxyajudazol A (3) is described. The isochromanone moiety present in the eastern fragment was constructed by an intramolecular-Diels-Alder (IMDA). Difficulti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10a1810977998e4eb1dbe3ae0c4d1b8e
https://doi.org/10.1021/jo302055w
https://doi.org/10.1021/jo302055w
Publikováno v:
Pure and Applied Chemistry. 84:1421-1433
Myxobacteria are an excellent source of novel secondary metabolites with a range of biological activities. This review details the synthesis of several examples of these natural products. The total synthesis of all the members of the crocacin family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6df4f488f8e57519c896d5887c335d28
https://doi.org/10.1351/pac-con-11-11-19
https://doi.org/10.1351/pac-con-11-11-19
Autor:
SiXuan Guo, Ryan Gilbert-Wilson, Anthony G. Wedd, Alan M. Bond, Jingli Xie, Stephen L. Birkett
Publikováno v:
Dalton Trans.. 40:356-366
Four salts have been isolated combining the triarylmethane dye cations pararosaniline (PR(+)) and crystal violet (CV(+)) with the hexametalates [M(6)O(19)](2-) (M = Mo, W). A new hexatungstic acid H(2)[W(6)O(19)]·4dma (dma = dimethylacetamide) was i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e402a0bffac4a3c0fa2406abcf69be15
https://doi.org/10.1039/c0dt00882f
https://doi.org/10.1039/c0dt00882f
Publikováno v:
ChemInform. 43
Myxobacteria are an excellent source of novel secondary metabolites with a range of biological activities. This review details the synthesis of several examples of these natural products. The total synthesis of all the members of the crocacin family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1ee3933cf263574caefb4f81b137237
https://doi.org/10.1002/chin.201247256
https://doi.org/10.1002/chin.201247256
Autor:
Mark A. Rizzacasa, Tim Quach, Danny Ganame, Stephen L. Birkett, Bill C. Hawkins, Sebastien Meiries
Publikováno v:
Organic letters. 13(8)
The total synthesis of a stereoisomer of 8-deshydroxyajudazol B (4), the putative biosynthetic intermediate of the ajudazols A (1) and B (2), is described. The key steps in the synthesis included an intramolecular Diels−Alder (IMDA) reaction to sec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6af88914cb2e79a763f70109488270bc
https://pubmed.ncbi.nlm.nih.gov/21410165
https://pubmed.ncbi.nlm.nih.gov/21410165