Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Dehimi Ouali"'
Publikováno v:
Journal of Thermal Analysis and Calorimetry. 147:5637-5648
Polystyrene/organo-Algerian montmorillonite hybrid material was prepared by radical copolymerization of styrene monomer in the presence of the double organic modified clay. Before copolymerization process, the local (Algerian) montmorillonite was sod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0c78c80efbff1ac734bc66f1f50124e
https://doi.org/10.1007/s10973-021-10935-8
https://doi.org/10.1007/s10973-021-10935-8
Publikováno v:
Journal of New Technology and Materials. 11:10-18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa8572ba501305cb217b29330d47afa5
https://doi.org/10.12816/0060294
https://doi.org/10.12816/0060294
Publikováno v:
International Journal of Intelligent Engineering and Systems. 11:266-274
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9b06af12257a40114669910bed3a1c9
https://doi.org/10.22266/ijies2018.0430.29
https://doi.org/10.22266/ijies2018.0430.29
Autor:
Lisa R Bennett, Arshed Mahmood, Jacqueline D Hewitt, John Leonard, Dehimi Ouali, Stephen J. Simpson
Publikováno v:
Tetrahedron. 58:4681-4691
The monoketal derived from cis-bicyclo[3.3.0]octane-3,7-dione was converted into the corresponding exo and endo epoxides. The meso exo epoxide was rearranged via enantioselective deprotonation using chiral lithium amide bases to provide a synthetical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92da1f95c49f825ef36eda6a4ad8f983
https://doi.org/10.1016/s0040-4020(02)00375-7
https://doi.org/10.1016/s0040-4020(02)00375-7
Autor:
John Leonard, Stephen J. Simpson, Jacqueline D Hewitt, Roger F. Newton, Dehimi Ouali, Shirley K. Rahman
Publikováno v:
ChemInform. 22
The monoketal derived from cis-bicyclo[3.3.0]octane-3,7-dione was deprotonated using chiral lithium amide bases and the enolates were trapped as either enol acetates or trimethylsilyl enol ethers. Oxidative cleavage of the enol derivatives provided u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71a63b8a8dfb0551e914fe0d02b83d34
https://doi.org/10.1002/chin.199108078
https://doi.org/10.1002/chin.199108078
Publikováno v:
ChemInform. 23
The monoketal derived from cis-bicyclo[3.3.0]octane-3,7-dione was converted to epoxides 3. The meso exo epoxide was cleaved via enantioselective deprotonation using chiral lithium amide bases to provide the synthetically useful alcohol 7 with up to 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9777fc8a75640c5008f1cfb626224f97
https://doi.org/10.1002/chin.199215059
https://doi.org/10.1002/chin.199215059
Publikováno v:
Journal of Chemical Research. 2000:176-178
Chiral polyfunctionalised cyclopentanes have been readily obtained in ~65% enantiomeric excess via a stereo-specific Wagner–Meerwein rearrangement induced by bromination of derivatives of the exo-cis Diels–Alder adduct of furan and maleic anhydri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2458ede0b845601c8e912a26629f81fe
https://doi.org/10.3184/030823400103166850
https://doi.org/10.3184/030823400103166850
Publikováno v:
Tetrahedron Letters. 31:6703-6706
The monoketal derived from cis-bicyclo[3.3.0]octane-3,7-dione was converted to epoxides 3. The meso exo epoxide was cleaved via enantioselective deprotonation using chiral lithium amide bases to provide the synthetically useful alcohol 7 with up to 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::414c4e9816ba80172f715dd0c44548ac
https://doi.org/10.1016/s0040-4039(00)97152-1
https://doi.org/10.1016/s0040-4039(00)97152-1
Autor:
Stephen J. Simpson, Dehimi Ouali, John Leonard, Roger F. Newton, Jacqueline D Hewitt, Shirley K. Rahman
Publikováno v:
Tetrahedron: Asymmetry. 1:699-702
The monoketal derived from cis-bicyclo[3.3.0]octane-3,7-dione was deprotonated using chiral lithium amide bases and the enolates were trapped as either enol acetates or trimethylsilyl enol ethers. Oxidative cleavage of the enol derivatives provided u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6faf0af1067be30e891d3955f80e1061
https://doi.org/10.1016/s0957-4166(00)82377-0
https://doi.org/10.1016/s0957-4166(00)82377-0
Publikováno v:
Tetrahedron Letters. 31:739-742
A short novel route to heteroyohimbine alkaloids is described. The key step in the process is the alkylation of a meso-ketone, during which its symmetry is broken. When chiral lithium amide bases are used for the ketone deprotonation encouraging leve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ee53a9e314498af00b6b1fcb86da76d
https://doi.org/10.1016/s0040-4039(00)94617-3
https://doi.org/10.1016/s0040-4039(00)94617-3