Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Charlotte M. Zammit"'
Autor:
James A. Bull, Stephanie Greed, Hannah R Cudmore, Charlotte M Zammit, Charlotte Leinfellner, Gregory B. Craven, Ruth R Tweedy, Alexander McDermott, Renzo Luisi, Edward L. Briggs, Dominic P. Affron, Alan Armstrong
Vinyl sulfones and sulfonamides are valued for their use as electrophilic warheads in covalent protein inhibitors. Conversely, the S(VI) aza-isosteres thereof, vinyl sulfoximines and sulfonimidamides, are far less studied and have yet to be applied t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70ed71366eee5439b33e03cebdbd8799
http://hdl.handle.net/10044/1/89673
http://hdl.handle.net/10044/1/89673
Autor:
Rachel K. O'Reilly, Rebecca J. Williams, Elena Lestini, Charlotte M. Zammit, Benoit Couturaud, Tao Chen, Maria Inam, Lewis D. Blackman
Publikováno v:
Polymer Chemistry. 9:820-823
Polymeric core–shell micelles incorporating a chiral palladium pyridinooxazoline catalyst are presented as nanoreactors for the aqueous asymmetric synthesis of flavanones, a class of flavonoids with therapeutic properties. Use of the nanoreactor wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25349af9d2055bacce708e662f4e1c55
https://doi.org/10.1039/c7py02050c
https://doi.org/10.1039/c7py02050c
Publikováno v:
Tetrahedron: Asymmetry. 27:208-221
The asymmetric synthesis of a range of 1,2-anti-1,5-syn-transpentacins, bearing either alkyl, phenyl or hydroxymethyl substituents at the C(5)-position, has been achieved using the diastereoselective conjugate additions of Grignard reagents to an ena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4b50fc02530265141904f1107239014
https://doi.org/10.1016/j.tetasy.2016.01.012
https://doi.org/10.1016/j.tetasy.2016.01.012
Autor:
Charlotte M. Zammit, Martin Wills
Publikováno v:
Tetrahedron: Asymmetry. 24:844-852
The cycloaddition of a chiral ligand containing a terminal alkyne to a soluble polymer containing an azide provides a convenient means for the attachment of an asymmetric transfer hydrogenation catalyst to a soluble polymer support. Using these ligan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea327b529e86988d001f3058f6b9bf4e
https://doi.org/10.1016/j.tetasy.2013.05.022
https://doi.org/10.1016/j.tetasy.2013.05.022
Autor:
Stephen G. Davies, Charlotte M. Zammit, Ai M. Fletcher, Myriam Y. Souleymanou, James A. Lee, James E. Thomson, Paul M. Roberts
Publikováno v:
ChemInform. 45
Enantiopure α-substituted β-amino acids are prepared by diastereoselective Ireland—Claisen rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27b5255238d6eec6acc3dde4a354dbcd
https://doi.org/10.1002/chin.201440088
https://doi.org/10.1002/chin.201440088
Publikováno v:
ChemInform. 44
Asymmetric syntheses of amino-methyl-cyclopentanecarboxylic acids are achieved in 9 steps from commercially available starting materials via Ireland-Claisen rearrangement of β-amino allyl esters (I), followed by ring-closure metathesis, reduction an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab9ee7b56cb613de8898578af2f6742d
https://doi.org/10.1002/chin.201348055
https://doi.org/10.1002/chin.201348055
Publikováno v:
Chemical communications (Cambridge, England). 49(63)
Asymmetric syntheses of (S,S,S)-2-amino-5-methylcyclopentanecarboxylic acid and (S,S,S)-2-amino-5-phenylcyclopentanecarboxylic acid were achieved in 9 steps from commercially available starting materials via the Ireland-Claisen rearrangement of two e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7192fb357de66b045ee67f394e95d61b
http://ora.ox.ac.uk/objects/uuid:c0a792d2-ea21-45c3-b50a-9335de9468c3
http://ora.ox.ac.uk/objects/uuid:c0a792d2-ea21-45c3-b50a-9335de9468c3
Autor:
Myriam Y. Souleymanou, Stephen G. Davies, James A. Lee, Paul M. Roberts, Charlotte M. Zammit, James E. Thomson, Ai M. Fletcher
Publikováno v:
Organic & Biomolecular Chemistry. 12:2702
The diastereoselective Ireland-Claisen rearrangement of a range of substituted allyl β-amino esters gave the corresponding enantiopure α-substituted-β-amino esters with good diastereoselectivity. The application of this methodology in the asymmetr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4634c9423086e736196ea77108aa37c0
https://doi.org/10.1039/c4ob00274a
https://doi.org/10.1039/c4ob00274a