Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jonathan Axon"'
Autor:
Glenn Mcenroe, Wolfgang Wick, Alison Murphy, Martin Uhl, Ann M. Kapoun, Andrew Lam, Heather K. Webb, Thomas-Toan Tran, Sundeep Dugar, Jonathan Axon, Steffen Aulwurm, Barry Patrick Hart, Linda S. Higgins, Jing Ying Ma, Venkataraman Sriram, Lisa Janssen, Sarvajit Chakravarty, Michael Weller, Darin E. Kizer, Andrew A. Protter, Darren H. Wong, Irene Kerr
Publikováno v:
Neuro-Oncology. 9:259-270
Transforming growth factor-beta (TGF-beta) is a proinvasive and immunosuppressive cytokine that plays a major role in the malignant phenotype of gliomas. One novel strategy of disabling TGF-beta activity in gliomas is to disrupt the signaling cascade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bdd7196e1e669e29fe4b1c79a10fd8a
https://doi.org/10.1215/15228517-2007-010
https://doi.org/10.1215/15228517-2007-010
Autor:
Terra D. Haddad, Rebecca Braslau, Marc O. Anderson, Armando Jimenez, Frank Rivera, Jonathan Axon
Publikováno v:
Tetrahedron. 58:5513-5523
The use of acyl hydrazines (hydrazides) as precursors for the stoichiometric generation of acyl radicals is explored. Two classes of substrates are examined: unsubstituted acyl hydrazines and acyl hydrazines substituted with a leaving group (2-nitrob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4426f571508c607cbc315e49610a76f
https://doi.org/10.1016/s0040-4020(02)00490-8
https://doi.org/10.1016/s0040-4020(02)00490-8
Publikováno v:
ChemInform. 25
N,N-disubstituted a-(xanthyl)-acetamides with an olefin on one of the substituents undergo cyclisation to a lactam by a radical chain reaction involving transfer of the xanthate group; anilides lead to the corresponding indolones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ae088b83ee4709017cfc7fea806e0e3
https://doi.org/10.1002/chin.199434074
https://doi.org/10.1002/chin.199434074
Publikováno v:
ChemInform. 26
The diastereoselectivity of radical addition to methyleneoxazolidinones depends on the nature of the addend radical and of the N-protecting group; the reaction provides a convenient enantioselective route to α-amino acids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfadb3b2e37c12c45150163d3c728957
https://doi.org/10.1002/chin.199541171
https://doi.org/10.1002/chin.199541171
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0c4df821e7ac7158e0fbfe492c9832a
https://doi.org/10.1002/chin.200035183
https://doi.org/10.1002/chin.200035183
Publikováno v:
J. Chem. Soc., Chem. Commun.. :549-550
The diastereoselectivity of radical addition to methyleneoxazolidinones depends on the nature of the addend radical and of the N-protecting group; the reaction provides a convenient enantioselective route to α-amino acids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad717bc331933362f6a7be9b2933e1e6
https://doi.org/10.1039/c39950000549
https://doi.org/10.1039/c39950000549