Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Eva G. Lovett"'
Autor:
Eva G. Lovett, Brian Halton
Publikováno v:
ChemInform. 22
Treatment of 6,6-dichloro-3-oxabicyclo[3.1.0]-hexane (7) with potassiumt-butoxide generates the ring-strained cyclopropene8 as a reactive intermediate. With 1,3-diphenylisobenzofuran compound8 is trapped as a ∼5∶1 mixture of theexo- andendo-adduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5065cb0a15fffb18ccbc663587282ca7
https://doi.org/10.1002/chin.199126172
https://doi.org/10.1002/chin.199126172
Autor:
Eva G. Lovett
Publikováno v:
ChemInform. 22
Stable quaternary ammonium alkoxides, a new type of organic strong base, were obtained from unhindered tertiary alkanolamines and glycidol. At elevated temperatures, the 2-hydroxyethyl derivatives underwent intramolecular rearrangements and deoxyalky
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5876f3da1b5ef8df1f297a8c92c4ed74
https://doi.org/10.1002/chin.199140104
https://doi.org/10.1002/chin.199140104
Autor:
Eva G. Lovett
Publikováno v:
The Journal of Organic Chemistry. 56:2755-2758
Stable quaternary ammonium alkoxides, a new type of organic strong base, were obtained from unhindered tertiary alkanolamines and glycidol. At elevated temperatures, the 2-hydroxyethyl derivatives underwent intramolecular rearrangements and deoxyalky
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f022e4ecebc37badac10df4d84c88428
https://doi.org/10.1021/jo00008a034
https://doi.org/10.1021/jo00008a034
Autor:
Eva G. Lovett, Brian Halton
Publikováno v:
Structural Chemistry. 2:147-152
Treatment of 6,6-dichloro-3-oxabicyclo[3.1.0]-hexane (7) with potassiumt-butoxide generates the ring-strained cyclopropene8 as a reactive intermediate. With 1,3-diphenylisobenzofuran compound8 is trapped as a ∼5∶1 mixture of theexo- andendo-adduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67ae0f6a352acaa04234c50131533c04
https://doi.org/10.1007/bf00676626
https://doi.org/10.1007/bf00676626
Publikováno v:
Parkinsonismrelated disorders. 7(3)
Water-soluble derivatives of buckminsterfullerene (C60) derivatives are a unique class of compounds with potent antioxidant properties. Studies on one class of these compounds, the malonic acid C60 derivatives (carboxyfullerenes), indicated that they
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da226180df2336e837549dfffc952515
https://pubmed.ncbi.nlm.nih.gov/11331193
https://pubmed.ncbi.nlm.nih.gov/11331193
Publikováno v:
Biopolymers. 38(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::911a1d1a47a7912c6384f70469a048dc
https://pubmed.ncbi.nlm.nih.gov/8722233
https://pubmed.ncbi.nlm.nih.gov/8722233
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34574d0bc79cf7e400c00b06461668a0
https://doi.org/10.1002/chin.199049191
https://doi.org/10.1002/chin.199049191
Publikováno v:
Tetrahedron Letters. 31:1313-1314
Treatment of the dihalo-3-oxabicyclohexane 1 with excess t-butoxide leads to the ring strained cyclopropene 3 . This is captured by diphenylisobenzofuran as Diels-Alder adduct 7 , whereas with furan only the ring expanded vinylcarbene 9 is intercepte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::594e77f3f5b1070c40d25cbb49e2863d
https://doi.org/10.1016/s0040-4039(00)88794-8
https://doi.org/10.1016/s0040-4039(00)88794-8
Autor:
David Lipkin, Eva G. Lovett
Publikováno v:
The Journal of Organic Chemistry. 42:2574-2580
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82fee083847171d3d2bcaa882a4e943c
https://doi.org/10.1021/jo00435a009
https://doi.org/10.1021/jo00435a009
Autor:
Eva G. Lovett, Rudy S. Buriks
Publikováno v:
The Journal of Organic Chemistry. 52:5247-5254
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f4ede6f0631d483f177948ffc27cc99
https://doi.org/10.1021/jo00232a035
https://doi.org/10.1021/jo00232a035