Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Andrea Arany"'
Autor:
Miklós Nyerges, David Bendell, Andrea Arany, David E. Hibbs, Simon J. Coles, Michael B. Hursthouse, Paul W. Groundwater, Otto Meth-Cohn
Publikováno v:
Tetrahedron. 61:3745-3753
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dda90d5c068ef56b94ff415b9eb2cc5
https://doi.org/10.1016/j.tet.2005.02.009
https://doi.org/10.1016/j.tet.2005.02.009
Autor:
Andrew C. Moralee, Jonathan M. Percy, Andrea Arany, Vittoria Salafia, Patrick Jelf Crowley, John Fawcett, Michael B. Hursthouse, Mark E. Light, Benson M. Kariuki
Publikováno v:
Org. Biomol. Chem.. 2:455-465
A difluorodienophile, synthesised using a Stille coupling reaction underwent tin(IV)-catalysed cycloaddition with three furans to afford oxa[2.2.1]bicycloheptenes in good yield. Reduction of ester and carbamate carbonyl groups and diol protection as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f72a3072cc60f0e770c78e14af53c9f
https://doi.org/10.1039/b314314g
https://doi.org/10.1039/b314314g
Autor:
Otto Meth-Cohn, David J. Bendell, David E. Hibbs, Miklós Nyerges, Andrea Arany, Michael B. Hursthouse, Paul W. Groundwater, Simon J. Coles
Publikováno v:
Synlett. :0947-0950
N-Metallated azomethine ylides were generated by the reaction of arylidene glycine imines with AgOAc and triethylamine. These azomethine ylides undergo cycloaddition to chiral acrylamides with excellent diastereoselectivity. The configuration of two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::984dcff5a42b0935d201fbc137d726ad
https://doi.org/10.1055/s-2003-39325
https://doi.org/10.1055/s-2003-39325
Autor:
David J. Bendell, László Tőke, Rosaleen J. Anderson, Miklós Nyerges, Weimin Zhang, Imre Fejes, Andrea Arany, Paul W. Groundwater
Publikováno v:
Tetrahedron. 58:989-995
The generation of N-substituted, stabilised azomethine ylides in the presence of N-phenylmaleimide gave the bicyclo[3.3.0] octane-3-carboxylate cycloadducts. In the absence of a dipolarophile, these azomethine ylides gave novel piperazine-6-carboxyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec91b4f542e54bea82ce576cfcb48725
https://doi.org/10.1016/s0040-4020(01)01184-x
https://doi.org/10.1016/s0040-4020(01)01184-x
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2605-2608
The generation of α,β∶γ,δ-unsaturated azomethine ylides 8 is described, starting from N-substituted α-amino acids 7 and aldehydes 6, 12. These azomethine ylides undergo a 1,7-electrocyclisation, followed by a [1,5]-hydrogen shift, to give the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41f9daef8d45369a2ce00d095f4aed7d
https://doi.org/10.1039/a904571f
https://doi.org/10.1039/a904571f
Autor:
Miklos Nyerges, Toqir Sharif, Paul W. Groundwater, David E. Hibbs, Michael B. Hursthouse, Andrea Arany
Publikováno v:
Tetrahedron Letters. 39:1433-1436
A novel synthesis of didehydroamino acid (DDAA) esters 4 is described, starting from aldimines 1 . The mechanism for this reaction involves the cycloaddition of an azomethine ylide 2 to an imine 1 , followed by the base-catalysed ring-opening of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::befa5a5d2fcb40e215e2598ee74841e4
https://doi.org/10.1016/s0040-4039(97)10821-8
https://doi.org/10.1016/s0040-4039(97)10821-8
Autor:
Miklos Nyerges, Andrea Arany, David E. Hibbs, Toqir Sharif, Ian Garnett, Paul W. Groundwater, Michael B. Hursthouse
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2837-2846
A novel synthesis of didehydroamino acid (DDAA) esters 5 is described, starting from aldimines 2. The mechanism for this reaction has been shown to involve the cycloaddition of an azomethine ylide 3 to an imine 2, followed by the base-catalysed ring-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bb9ca1ac1e5e8b73ff180f4670a88ef
https://doi.org/10.1039/a803695k
https://doi.org/10.1039/a803695k
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f5fa2d4a1b60847a496f27fda196e1a
https://doi.org/10.1002/chin.199832215
https://doi.org/10.1002/chin.199832215
Autor:
Miklos Nyerges, Andrea Arany, Toqir Sharif, Paul W. Groundwater, Michael B. Hursthouse, Ian Garnett, David E. Hibbs
Publikováno v:
ChemInform. 30
A novel synthesis of didehydroamino acid (DDAA) esters 5 is described, starting from aldimines 2. The mechanism for this reaction has been shown to involve the cycloaddition of an azomethine ylide 3 to an imine 2, followed by the base-catalysed ring-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23aec50ae092059f8e8aa9ce9eb73ea9
https://doi.org/10.1002/chin.199903086
https://doi.org/10.1002/chin.199903086
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc95b288247e01cc33229f4f9e551728
https://doi.org/10.1002/chin.199952169
https://doi.org/10.1002/chin.199952169