Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Robert J. Blade"'
Publikováno v:
Tetrahedron Letters. 28:3857-3860
Novel stereoselective routes to new arylpolyene isobutylamides are described. A range of non-natural unsaturated amides has been synthesised.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5daaf96a2f0d1b8b5b32a81696554337
https://doi.org/10.1016/s0040-4039(00)96405-0
https://doi.org/10.1016/s0040-4039(00)96405-0
Publikováno v:
Tetrahedron Letters. 28:4879-4882
Syntheses of 10,11-dehydro- and 10,11-( Z )-pipercide, piperovatin, and an ene-yne, and a perfluoro-isobutylamide, illustrate the utility of hydrozirconation methodology in this area.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd3f3f29694c41967238939705eeb5f7
https://doi.org/10.1016/s0040-4039(00)96650-4
https://doi.org/10.1016/s0040-4039(00)96650-4
Publikováno v:
Tetrahedron Letters. 28:4875-4878
Hydrometallation of α,ω-diynes is used to make ω-acetylenic isobutylamide synthons: new syntheses of anacyclin, pellitorine and its vinylogous triene are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3914200d178485d981c5fe9e36be8c53
https://doi.org/10.1016/s0040-4039(00)96649-8
https://doi.org/10.1016/s0040-4039(00)96649-8
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::103d880861bf115c682ab0a07150b50c
https://doi.org/10.1002/chin.198805180
https://doi.org/10.1002/chin.198805180
Publikováno v:
ChemInform. 19
Hydrometallation of α,ω-diynes is used to make ω-acetylenic isobutylamide synthons: new syntheses of anacyclin, pellitorine and its vinylogous triene are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c19c1b17655df294c802d2fa422f4534
https://doi.org/10.1002/chin.198812345
https://doi.org/10.1002/chin.198812345
Autor:
Robert J. Blade, Philip Hodge
Publikováno v:
Chemischer Informationsdienst. 10
A 12-step synthetic route to (±)-daunomycinone is described which uses Friedel–Crafts reactions to assemble the ring system; (–)-carminomycinone reacts with diazomethane to give (+)-daunomycinone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b4f85fa9bc28e430d299114aad4ca94
https://doi.org/10.1002/chin.197921337
https://doi.org/10.1002/chin.197921337
Publikováno v:
ChemInform. 20
The reactivity of the trifluoromethylating system copper-dibromodifluoromethane-N, N-dimethylacetamide towards aryl chlorides can be enhanced by the addition of charcoal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84857c8b68fceeaebb135666a8629f38
https://doi.org/10.1002/chin.198948094
https://doi.org/10.1002/chin.198948094
Autor:
Robert J. Blade, Philip Hodge
Publikováno v:
J. Chem. Soc., Chem. Commun.. :85-86
A 12-step synthetic route to (±)-daunomycinone is described which uses Friedel–Crafts reactions to assemble the ring system; (–)-carminomycinone reacts with diazomethane to give (+)-daunomycinone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b52852827bdcdc25478466f4f3550b13
https://doi.org/10.1039/c39790000085
https://doi.org/10.1039/c39790000085
Autor:
Christopher A. Ramsden, Alan R. Katritzky, Sukhpal S. Thind, Pai-Lin Nie, Jayant B. Bapat, Bernard P. Leddy, Robert J. Blade
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :418
Benzylamine and 2-, 3-, and 4-pyridylmethylamine are readily converted into the corresponding 1-substituted 2,4,6-triphenylpyridinium cations, from which 2,4,6-triphenylpyridine is displaced in high yield by a variety of nucleophiles. This synthetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae6864b7c2cd79b86737c505d052ddf4
https://doi.org/10.1039/p19790000418
https://doi.org/10.1039/p19790000418