Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Alexander V. W. Mayweg"'
Autor:
Victor Y. Lee, Robert M. Adlington, Dirk Schwaebisch, Jack E. Baldwin, Alexander V. W. Mayweg, Thomas W. Fenlon
Publikováno v:
Synlett. 2007:2679-2682
Investigation towards the synthesis of the furanosesquiterpene Lindenene using an intramolecular cyclopropanation reaction gave unexpected ring-junction isomerisation products. These products were elaborated to (±)-epi- lindenene and (±)-iso-linden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53efe158335b52289da0249e8c8745d
https://doi.org/10.1055/s-2007-991069
https://doi.org/10.1055/s-2007-991069
Publikováno v:
Organic Letters. 7:79-82
Treatment of highly potent and densely functionalized bryostatin analogue 1 with dimethyldioxirane afforded the C-9 hydroxylated hemiketal 2 via oxyfunctionalization of the C9-CH bond, one of 12 CH bonds geminal to an oxygen substituent in 1. When br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65e07d4ef16dbcf016f93951f139a12c
https://doi.org/10.1021/ol047859w
https://doi.org/10.1021/ol047859w
Autor:
Robert M. Adlington, Alexander V. W. Mayweg, Jack E. Baldwin, Fanny Roussi, Rodolfo Marquez, Paul G. Bulger
Publikováno v:
Tetrahedron. 57:7409-7416
Intramolecular cyclisations of dimeric bis-anhydride compounds have been investigated, to help elucidate the biosynthesis of the nonadride family of compounds. Short and efficient syntheses of these bis-anhydride compounds, together with their cyclis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50dbab6543577fe211136bea9625bc71
https://doi.org/10.1016/s0040-4020(01)00706-2
https://doi.org/10.1016/s0040-4020(01)00706-2
Publikováno v:
Organic Letters. 4:3009-3011
[reaction: see text] A study toward a possible biomimetic hetero Diels-Alder reaction is reported between humulene and a novel tropolone ortho-quinone methide. A suitable tropolone ortho-quinone methide precursor has been prepared from 3-methyl-2-fur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34bad678b0c8faeb6f0a87e14a8a8f0d
https://doi.org/10.1021/ol026467r
https://doi.org/10.1021/ol026467r
Autor:
Robert M. Adlington, Dirk Schwaebisch, Victor Y. Lee, Jack E. Baldwin, Alexander V. W. Mayweg, Thomas W. Fenlon
Publikováno v:
ChemInform. 39
Investigation towards the synthesis of the furanosesqui-terpene Lindenene using an intramolecular cyclopropanation reaction gave unexpected ring-junction isomerisation products. These products were elaborated to (±)- EPI-lindenene and (±)- ISO-lind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::466483343c9091791fd8772aac65ecf3
https://doi.org/10.1002/chin.200810199
https://doi.org/10.1002/chin.200810199
Publikováno v:
ChemInform. 34
An expedient ten-step synthesis of a substituted tropolone is described. The synthesis involves a 3-oxidopyrylium [5+2] cycloaddition reaction with acrylonitrile as the key step, affording a highly functionalized [3.2.1]-bicycle 10 as a single regioi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c8853351fb5d11d62e754cd6577664f
https://doi.org/10.1002/chin.200338053
https://doi.org/10.1002/chin.200338053
Publikováno v:
Organic letters. 1(12)
Analogues of the tropolone natural products pycnidione and epolone B were synthesized via a hetero Diels−Alder reaction of benzotropolone 10 with humulene. The quinone methide benzotropolone 13 was generated in situ by thermalisation of benzotropol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b588066e6cbfccacb11885a6a6174f16
https://pubmed.ncbi.nlm.nih.gov/10905860
https://pubmed.ncbi.nlm.nih.gov/10905860