Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Kristína Csatayová"'
Autor:
James A. Lee, Alice M. R. Kennett, Ai M. Fletcher, Marta Brambilla, Paul M. Roberts, James E. Thomson, Stephen G. Davies, Méabh B. Brennan, Kristína Csatayová, Angela J. Russell
Publikováno v:
The Journal of Organic Chemistry. 82:10297-10309
The diastereoselectivities and rates of epoxidation (upon treatment with Cl3CCO2H then m-CPBA) of a range of cis- and trans-4-aminocycloalk-2-en-1-ol derivatives (containing five-, six-, and seven-membered rings) have been investigated. In all cases
Autor:
Stephen G. Davies, Ai M. Fletcher, David J. Klauber, James E. Thomson, Paul M. Roberts, J. Gair Ford, Kristína Csatayová
Publikováno v:
Tetrahedron. 71:7170-7180
Diastereoselective syn- and anti-dihydroxylations of enantiopure tetrahydropyridine and tetrahydroazepine scaffolds have been used in total asymmetric syntheses of the polyhydroxylated azacycles (−)-fagomine, (−)-3-epi-fagomine, (−)-5-epi-fagom
Autor:
Kristína Csatayová, William D. Green, Stephen G. Davies, James A. Lee, James E. Thomson, Ai M. Fletcher, Méabh B. Brennan, Paul M. Roberts, Angela J. Russell
Publikováno v:
The Journal of Organic Chemistry. 80:6609-6618
Diastereoselective syntheses of dihydroconduramines (±)-B-1, (±)-E-1, and (±)-F-1 have been achieved from N-protected 4-aminocyclohex-2-en-1-ols via two complementary procedures for epoxidation as the key step. Treatment of either trans- or cis-4-
Autor:
Matthew S. Kennedy, Ai M. Fletcher, James E. Thomson, Stephen G. Davies, Kristína Csatayová, Thomas R. Fowler, Paul M. Roberts
Publikováno v:
Journal of Organic Chemistry. 82(23)
The asymmetric syntheses of a range of N- and O-protected 3-deoxy-3-aminosphingoid bases have been achieved using two complementary approaches. dl-Serine was converted to a racemic N,N-dibenzyl-protected γ-amino-α,β-unsaturated ester which was res
Autor:
Paul M. Roberts, J. Gair Ford, Stephen G. Davies, Kristína Csatayová, James E. Thomson, James A. Lee
Publikováno v:
The Journal of Organic Chemistry. 78:12397-12408
Ab initio asymmetric syntheses of methyl N,O-diacetyl-D-3-epi-daunosaminide and methyl N,O-diacetyl-D-ristosaminide, employing diastereoselective epoxidation and dihydroxylation, respectively, of alkyl (3S,αR,Z)-3-[N-benzyl-N-(α-methylbenzyl)amino]
Autor:
James E. Thomson, Kristína Csatayová, Paul M. Roberts, James A. Lee, Kirsten E. Christensen, Stephen G. Davies, Amber L. Thompson
Crystals of benzyl (RS,RS,RS)-7-phenylbicyclo[5.1.0]octan-2-ylcarbamate 9 and (RS,RS,RS)-N-[3′-(4″-methylpiperazin-1″-yl)propyl]-N-{5-(4′′′-cyanophenyl)bicyclo[3.1.0]hexan-2-yl}amine dihydrochloride 10·2HCl were synthesised and single cr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e9ff4002442e0605d7ac97a4761997a
https://ora.ox.ac.uk/objects/uuid:e466e4eb-6328-4670-a03d-0dc3c3855fc8
https://ora.ox.ac.uk/objects/uuid:e466e4eb-6328-4670-a03d-0dc3c3855fc8
Autor:
Paul M. Roberts, James A. Lee, Angela J. Russell, Kenneth B. Ling, Kristína Csatayová, Stephen G. Davies, James E. Thomson
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SCH-A and cis-SCH-A. This strategy encompasses a stereodivergent procedure for the preparation of syn- and anti-cyclopropane diastereoisomers in high dr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81cf3d82e9251bd56acf25041e3f3011
https://doi.org/10.1021/ol101295t
https://doi.org/10.1021/ol101295t
Autor:
Angela J. Russell, James A. Lee, Paul M. Roberts, Stephen G. Davies, Kristína Csatayová, Kenneth B. Ling, James E. Thomson
A highly chemo- and diastereoselective protocol for the cyclopropanation of tertiary allylic amines with Shi's carbenoid [CF 3CO 2ZnCH 2I] is described. The high levels of diastereoselectivity observed in these reactions may be attributed to chelatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0323659fac6f645894beed8f862ee7be
https://ora.ox.ac.uk/objects/uuid:904d0097-cea5-448e-b541-4b04a1ed5cb7
https://ora.ox.ac.uk/objects/uuid:904d0097-cea5-448e-b541-4b04a1ed5cb7
Autor:
Ian T. T. Houlsby, Sam M. Rowe, Ai M. Fletcher, Marek Buchman, James E. Thomson, Kristína Csatayová, Stephen G. Davies, Paul M. Roberts
Publikováno v:
Journal of Organic Chemistry. 81(12)
Efficient de novo asymmetric syntheses of (+)-preussin B, the C(2)-epimer of (-)-preussin B, and 3-deoxy-(+)-preussin B have been developed, using the diastereoselective conjugate addition of lithium (S)-N-benzyl-N-(α-methylbenzyl)amide to tert-buty
Autor:
David J. Klauber, Ai M. Fletcher, Stephen G. Davies, James E. Thomson, Paul M. Roberts, J. Gair Ford, Kristína Csatayová
Publikováno v:
ChemInform. 46
The target compounds are synthesized using diastereoselective olefinic oxidations of enantiopure tetrahydropyridines.