Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Andrew J. Wildsmith"'
Autor:
Andrew J. Wildsmith, Mark J. Burk, Julian P. Henschke, Daniela Herzberg, Christopher J. Cobley, Justine A. Peterson, Christophe G. Malan, Guy Casy
Publikováno v:
Advanced Synthesis & Catalysis. 345:300-307
The novel biaryldiphosphine ligand 1 (Hexa- PHEMP) has been prepared in five steps from commercially available 3,4,5-trimethylphenol using a concise synthetic route. This approach also allows fine tuning of the ligand×s stereoelectronic properties t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2ca445abba152cacdfbfeba729f7424
https://doi.org/10.1002/adsc.200390025
https://doi.org/10.1002/adsc.200390025
Publikováno v:
Tetrahedron Letters. 42:3239-3242
Attempted tandem allylic acetate isomerisation and ring-closing metathesis using combinations of palladium(0)/Grubbs’ catalyst/PPh 3 led to either allylic isomerisation or ring-closing metathesis but not both in tandem. The effect was traced to dea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4083233689f5befbbd0d34c6f25e9822
https://doi.org/10.1016/s0040-4039(01)00405-1
https://doi.org/10.1016/s0040-4039(01)00405-1
Autor:
Sofia I. Pascu, Andrew B. Holmes, Andrew N. Payne, Andrew J. Wildsmith, Miles Congreve, Craig L. Francis, Neil Roy Curtis, S. Y. Frankie Mak, Jonathan W. Burton, John E. Davies
Publikováno v:
ChemInform. 39
An enantioselective synthesis of the halogenated medium-ring ether natural product (+)-obtusenyne is reported which uses the ring expansion of a seven-membered ketene acetal by means of a Claisen rearrangement to construct the core nine-membered oxyg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa6f6bd1a1c99eb1f699d8cce05e1311
https://doi.org/10.1002/chin.200833203
https://doi.org/10.1002/chin.200833203
Autor:
Andrew N. Payne, John E. Davies, Craig L. Francis, Sofia I. Pascu, Neil Roy Curtis, S. Y. Frankie Mak, Andrew B. Holmes, Miles Congreve, Andrew J. Wildsmith, Jonathan W. Burton
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 14(9)
An enantioselective synthesis of the halogenated medium-ring ether natural product (+)-obtusenyne is reported which uses the ring expansion of a seven-membered ketene acetal by means of a Claisen rearrangement to construct the core nine-membered oxyg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77eafb4397fc276ac3d24fd467f177a
http://ora.ox.ac.uk/objects/uuid:e77c401b-8833-46f5-b9dc-0093b2c598a9
http://ora.ox.ac.uk/objects/uuid:e77c401b-8833-46f5-b9dc-0093b2c598a9