Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Simon W. Ainge"'
Publikováno v:
Helvetica Chimica Acta. 85:417-430
Two novel, potentially antimicrobial erythronolide aglycon analogs ((-)-9 and (-)-30, respectively), which incorporate a large number of contiguous stereogenic centers, have been prepared by multistep synthesis from simple chirons. The chemistry pres
Autor:
Simon W. Ainge, Pierre Vogel
Publikováno v:
Tetrahedron Letters. 39:4039-4042
The Diels-Alder adduct of 2,4-dimethylfuran to 1-cyanovinyl (1'S)-camphanate was converted into (2R,3R,4S,5S,6R,7R)-3,6-epoxy-4,5-isopropylidenedioxy-2,4,6-trimethyl-7- [(tert-butyl)-dimethylsilyloxy]non-1-yl phenyl sulfoxides (6), the condensation o
Autor:
Pierre Vogel, Simon W. Ainge
Publikováno v:
ChemInform. 29
The Diels-Alder adduct of 2,4-dimethylfuran to 1-cyanovinyl (1'S)-camphanate was converted into (2R,3R,4S,5S,6R,7R)-3,6-epoxy-4,5-isopropylidenedioxy-2,4,6-trimethyl-7- [(tert-butyl)-dimethylsilyloxy]non-1-yl phenyl sulfoxides (6), the condensation o
Autor:
Simon J. Harwood, David M. Hollinshead, Julian G. Knight, Andrew M. Harm, Haydn I. Maughan, Simon W. Ainge, Albert A. Jaxa-Chamiec, Armour Duncan Robert
Publikováno v:
ChemInform. 31
Publikováno v:
ChemInform. 32
Publikováno v:
ChemInform. 33
Two novel, potentially antimicrobial erythronolide aglycon analogs ((-)-9 and (-)-30, respectively), which incorporate a large number of contiguous stereogenic centers, have been prepared by multistep synthesis from simple chirons. The chemistry pres
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :3188-3190
Palladium catalysed carbonylation of both 4-alkynyl-1,3-dioxolan-2-ones and alkynyl epoxides occurs under mild conditions to give methyl 5-hydroxy-2,3-dienoates which are converted to γ,δ-unsaturated δ-lactones by tandem conjugate addition–cycli
Autor:
Albert A. Jaxa-Chamiec, Julian G. Knight, Simon J. Harwood, Armour Duncan Robert, and David M. Hollinshead, Haydn I. Maughan, Andrew M. Harm, Simon W. Ainge
Publikováno v:
Journal of the American Chemical Society. 122:2944-2945