Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jon D. Elsworth"'
Publikováno v:
Org. Biomol. Chem.. 8:751-754
New and simple protocols are described for the conversion of the enzymatically-derived and enantiomerically pure cis-1,2-dihydrocatechol 7 (X = I) and its 6-methylated derivative into either antipodal form of compounds embodying the tricyclic framewo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811f7504dd3bdb57be337398029ea72a
https://doi.org/10.1039/b921600f
https://doi.org/10.1039/b921600f
Publikováno v:
Organic Letters. 8:3319-3322
[Structure: see text] The total synthesis of the marine metabolite clavosolide A is reported which confirms the structure and absolute configuration of the natural product as the symmetrical diolide glycosylated by permethylated D-xylose moieties, 2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7abea4f2bc61d061789f41db267440ba
https://doi.org/10.1021/ol0611705
https://doi.org/10.1021/ol0611705
Autor:
Christopher D. Bailey, Sophie J. Edwards, Jon D. Elsworth, Tshepo Pheko, Christine L. Willis, Adam J. Bunt, Benjamin D. Cons
Publikováno v:
Angewandte Chemie (International ed. in English). 51(16)
trans-2,8-Dioxabicyclodecanes were prepared in high yield with the creation of up to three stereocenters in a single pot by the acid-mediated reaction of γ,δ-unsaturated alcohols with aldehydes (see scheme, Bn=benzyl). This versatile reaction enabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac9616c9c0e9b965e0e057d0c581a684
https://pubmed.ncbi.nlm.nih.gov/22392806
https://pubmed.ncbi.nlm.nih.gov/22392806
Autor:
Jon D. Elsworth, Christine L. Willis
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3aa983f7a33fa50145363c13a4b8dbbe
https://doi.org/10.1002/chin.200832136
https://doi.org/10.1002/chin.200832136
Autor:
Jon D. Elsworth, Christine L. Willis
Publikováno v:
Chemical communications (Cambridge, England). (13)
Methyl (4E,7R)-7-hydroxyoctanoate was prepared in 71% yield from ethyl (R)-3-hydroxybutanoate and on reaction with a series of aldehydes in the presence of TMSOTf gave bicyclic oxygen heterocycles in good yields and with the creation of three new ste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6366d8633e0c1984b69699671558ff8c
https://pubmed.ncbi.nlm.nih.gov/18354808
https://pubmed.ncbi.nlm.nih.gov/18354808
Autor:
Nick Bushby, Conor S. Barry, Jon D. Elsworth, Roger W. Alder, John R. Harding, Christine L. Willis, Peter T. Seden
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2080e019839590baee47510a29106d74
https://doi.org/10.1002/chin.200641197
https://doi.org/10.1002/chin.200641197
Autor:
Jon D. Elsworth, Conor S. Barry, Jonathan P. H. Charmant, Christine L. Willis, John R. Harding, Nick Bushby
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dd7cd5057258df1026abe667c86d85e
https://doi.org/10.1002/chin.200610211
https://doi.org/10.1002/chin.200610211
Autor:
Conor S. Barry, Jonathan P. H. Charmant, John R. Harding, Nick Bushby, Jon D. Elsworth, Christine L. Willis
Publikováno v:
Chemical communications (Cambridge, England). (40)
The first total synthesis of the reported structure of the sponge metabolite clavosolide A is described using a Prins cyclisation to assemble the tetrahydropyran core followed by manipulation of the side-chain, dimerisation and finally glycosidation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1daef72c6cd182c5d6b88c0224db12c3
https://pubmed.ncbi.nlm.nih.gov/16220183
https://pubmed.ncbi.nlm.nih.gov/16220183