Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jose Luis Martos"'
Publikováno v:
Tetrahedron Letters. 40:1575-1578
Ethyl 4,4-dimethylpyroglutamate has been used as a chiral auxiliary for α,β-unsaturated acids in Michael addition reactions. The conjugate addition of Grignard reagents to the amides in the presence of copper iodide, tetramethylene diamine (TMEDA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::363e9d1dcc11f6b03e2d3eea3bb9f70c
https://doi.org/10.1016/s0040-4039(98)02648-3
https://doi.org/10.1016/s0040-4039(98)02648-3
Publikováno v:
ChemInform. 30
A reduction of the tetracyclic skeleton of sordarins and sordaricins to a cyclopentane ring bearing the pharmacophore functional groups led to new derivatives retaining part of their in vitro and whole-cell activity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f2ad37fd1aa82f768afbf36e73c6220
https://doi.org/10.1002/chin.199919255
https://doi.org/10.1002/chin.199919255
Publikováno v:
ChemInform. 30
Ethyl 4,4-dimethylpyroglutamate has been used as a chiral auxiliary for α,β-unsaturated acids in Michael addition reactions. The conjugate addition of Grignard reagents to the amides in the presence of copper iodide, tetramethylene diamine (TMEDA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68bb383cd6764ebdbce1758ad579fd45
https://doi.org/10.1002/chin.199921040
https://doi.org/10.1002/chin.199921040
Publikováno v:
CEU Repositorio Institucional
instname
instname
En: Bioorganic and Medicinal Chemistry Letters. ISSN 0960-894x. n. 9, 1999, págs 103-108 A reduction of the tetracyclic skeleton of sordarins and sordaricins to a cyclopentane ring bearing the pharmacophore functional groups led to new derivatives r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07746ec1c1159b210f9f7a7dcf999b66
https://pubmed.ncbi.nlm.nih.gov/9990465
https://pubmed.ncbi.nlm.nih.gov/9990465