Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M. G. Pausler"'
Autor:
J. B. J. Milbank, M. G. Pausler, Richard C. Cambie, J. M. Coddington, Peter S. Rutledge, P. I. Sinkovich, J. J. Rustenhoven, G. L. Shaw
Publikováno v:
ChemInform. 24
The enolates of (+)- and (-)- menthyl acetate, formed by transmetallation from lithium with chloro ( cyclopentadienyl )bis(1,2:5,6-di-O-isopropylidene-α-D-glucofuranosato-O3)titanium [ CpTi (DAGO)2Cl] (1), react with benzaldehyde from the Re-face wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b1e62ef88b11b419461f84b8a6bf1c7
https://doi.org/10.1002/chin.199336053
https://doi.org/10.1002/chin.199336053
Autor:
M. G. Pausler, P. S. Rutledge
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43e27416ccb0cd9afe6bb8830e4db453
https://doi.org/10.1002/chin.199521279
https://doi.org/10.1002/chin.199521279
Autor:
M. G. Pausler, P. S. Rutledge
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af70136b0dd1ee05d115e437294c0294
https://doi.org/10.1002/chin.199521278
https://doi.org/10.1002/chin.199521278
Autor:
P. I. Sinkovich, M. G. Pausler, G. L. Shaw, Richard C. Cambie, J. B. J. Milbank, J. J. Rustenhoven, J. M. Coddington, Peter S. Rutledge
Publikováno v:
Australian Journal of Chemistry. 46:583
The enolates of (+)- and (-)- menthyl acetate, formed by transmetallation from lithium with chloro ( cyclopentadienyl )bis(1,2:5,6-di-O-isopropylidene-α-D-glucofuranosato-O3)titanium [ CpTi (DAGO)2Cl] (1), react with benzaldehyde from the Re-face wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e432733e7fd4c61ae02f118b614ee528
https://doi.org/10.1071/ch9930583
https://doi.org/10.1071/ch9930583
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4430f681e102ec53d9081896043d4f2
https://doi.org/10.1002/chin.198608141
https://doi.org/10.1002/chin.198608141
Publikováno v:
Australian Journal of Chemistry. 40:1063
Anthrarufin (4) has been converted by a high-yielding route involving sequential reductive Claisen rearrangements into 1-acetoxy-5-methoxy-9,10-dioxo-6-(2'-oxopropy1)-9,10-dihydroanthracene-2-carbaldehyde (3), an intermediate which is suitable for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2532514840bd6101bd10c0f125de345
https://doi.org/10.1071/ch9871063
https://doi.org/10.1071/ch9871063