Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Eleanor F. Duffy"'
Publikováno v:
Tetrahedron. 63:2047-2052
Herein we described the preparation of two novel heterocyclic nuclei isoxazolopyridone and pyrazolopyridone. The syntheses are modular in nature and fast to execute. The title compounds were obtained pure without intervention of chromatography.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2342c637d1eb2a18e5ffbc71048241e
https://doi.org/10.1016/j.tet.2006.12.044
https://doi.org/10.1016/j.tet.2006.12.044
Autor:
Eleanor F. Duffy, Mauro F. A. Adamo
Publikováno v:
Organic Letters. 8:5157-5159
A four component one-pot procedure (4-MC) was developed to assemble 3-heteroarylpropionic acids from commercially available materials. This new methodology affords the title compounds in high yields and without the use of chromatography. [reaction: s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21379bbf424c772d08f0bcf5b3352a4c
https://doi.org/10.1021/ol062151y
https://doi.org/10.1021/ol062151y
Publikováno v:
ChemInform. 38
A high yielding synthesis of polyfunctional scaffold 3-methyl-4-nitro-5-heteroarylethenylisoxazole is described. The novel condition allowed the preparation of reactive title compounds in high yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0b6824efdf2979e5181639788e615f9
https://doi.org/10.1002/chin.200740129
https://doi.org/10.1002/chin.200740129
Publikováno v:
ChemInform. 38
Herein we described an optimised synthesis of isoxazoloazepinone and novel heterocycle pyrazoloazepinone. These syntheses are modular in nature and fast to execute. The title compounds were obtained pure without the intervention of chromatography.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8d29b23d424ca9341bbb98c10712337
https://doi.org/10.1002/chin.200727140
https://doi.org/10.1002/chin.200727140
Publikováno v:
ChemInform. 37
A three-component one-pot procedure (3-MCR) was developed to assemble the spiroisoxazoline nucleus from commercially available materials. This new methodology affords the title compounds in high yields and without the use of chromatography.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d006fa298231b7d1285e4a5b64fe709c
https://doi.org/10.1002/chin.200607137
https://doi.org/10.1002/chin.200607137