Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Thomas G. R. Sellers"'
Autor:
Thomas G. R. Sellers, John Fox, Miguel A. Sanz, Fátima C. Teixeira, Anne J. Price, Simon Jones, Andrew D. Smith, Stephen G. Davies
Publikováno v:
Scopus-Elsevier
The rearrangement of a range of N-benzyl-O-allylhydroxylamines to the corresponding N-allylhydroxylamines upon treatment with n-BuLi in THF, followed by reduction to the corresponding N-allylamines, is described. Mechanistic studies of the transforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6149105daea828055fda54c4a5598919
https://doi.org/10.1039/b205323n
https://doi.org/10.1039/b205323n
Autor:
Steven D. Bull, Sara Hernández Domíngez, Stephen G. Davies, Simon Jones, Anne J. Price, Thomas G. R. Sellers, Andrew D. Smith
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2141-2150
The diastereoselective [2,3]-sigmatropic rearrangements of lithium N-benzyl-O-allylhydroxylamides bearing a stereogenic centre adjacent to the migration terminus are examined. (E)-N-Benzyl-O-(4-phenylpent-2-enyl)-hydroxylamine rearranges in 30% de to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17e038ddcb7808fc3dbf0a147d37e5cf
https://doi.org/10.1039/b207069n
https://doi.org/10.1039/b207069n
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b5747468c40f4db5f4a9c03203879b6
https://doi.org/10.1002/chin.200041250
https://doi.org/10.1002/chin.200041250
Publikováno v:
Current Trends in Organic Synthesis ISBN: 9781461371755
Chiral auxiliaries and templates are effective tools for the asymmetric synthesis of homochiral molecules.1 Most chiral auxiliaries are small heterocyclic compounds which rely on sterically demanding functional groups to control the conformation of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f612d9b9d4c2bb2bd2140fd427d658e
https://doi.org/10.1007/978-1-4615-4801-0_1
https://doi.org/10.1007/978-1-4615-4801-0_1
Publikováno v:
TETRAHEDRON-ASYMMETRY. 9(9)
Alkylation studies on the enolate of N -methyl morpholinone 7 clearly reveal that the observed cis -selectivity is consistent with a chiral relay system operating to invert the stereochemical information of the auxiliary's C 5 stereogenic centre.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41004aede2aad1fc86605dd0142afb16
http://ora.ox.ac.uk/objects/uuid:3ba1f17d-de26-4c70-9140-f8819d434a6e
http://ora.ox.ac.uk/objects/uuid:3ba1f17d-de26-4c70-9140-f8819d434a6e
Autor:
Stephen G. Davies, Juan A. Tamayo, Andrew D. Smith, A. Christopher Garner, Alastair L. Parkes, Paul M. Roberts, Steven D. Bull, James E. Thomson, Thomas G. R. Sellers, Richard Vickers
Publikováno v:
New Journal of Chemistry. 31:486
High levels of diastereoselectivity are observed for benzylation of the lithium enolates of (S)-N,N′-bis-para-methoxybenzyl-3-iso-propyl- piperazine-2,5-dione, (S)-N(1)-para-methoxybenzyl-N(4)-methyl-3-iso-propyl- piperazine-2,5-dione and (S)-N(1)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1156861187f6e111fb789f2226e8c6
https://doi.org/10.1039/b701628j
https://doi.org/10.1039/b701628j
Autor:
Steven D. Bull, Stephen G. Davies, A. Christopher Garner, Alastair L. Parkes, Paul M. Roberts, Thomas G. R. Sellers, Andrew D. Smith, Juan A. Tamayo, James E. Thomson, Richard J. Vickers
Publikováno v:
New Journal of Chemistry; Apr2007, Vol. 31 Issue 4, p486-495, 10p