Zobrazeno 1 - 9
of 9
pro vyhledávání: '"R. F. O. Warren"'
Publikováno v:
Journal of Inorganic and Organometallic Polymers. 1:361-375
The synthesis and characterization of siloxanes containing methacrylate, epoxy, and amino side chains are described. Direct hydrosilylation of unsaturated methacrylate or epoxy compounds with methyl hydrogen siloxanes resulted in the attachment of me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fe934597651e34370deb1c73220e644
https://doi.org/10.1007/bf00702499
https://doi.org/10.1007/bf00702499
Publikováno v:
Synthesis. 1986:845-847
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c3630933214e8c133a6e7bf64d069ac
https://doi.org/10.1055/s-1986-31800
https://doi.org/10.1055/s-1986-31800
Autor:
R. A. Massy-Westropp, R. F. O. Warren
Publikováno v:
Chemischer Informationsdienst. 16
3-Nonylidenetetrahydrofuran is readily reduced with lithium and ethanol in ammonia to yield mainly 3-nonyltetrahydrofuran together with 3-methyldodecan-1-ol. The reductions of a mixture of 4-nonyl-4,5-dihydrofuran and 3-nonyl-2,Sdihydrofuran and of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6522a6ce41cda924ac1d7ec3ba246644
https://doi.org/10.1002/chin.198506189
https://doi.org/10.1002/chin.198506189
Publikováno v:
ChemInform. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94408ae4c7ec1913bb16a86eaeb66c4b
https://doi.org/10.1002/chin.198711120
https://doi.org/10.1002/chin.198711120
A phenazine antibiotic (mp, 243 to 244 degrees C), isolated in a yield of 134 micrograms/ml from cultures of Pseudomonas fluorescens 2-79 (NRRL B-15132), was indistinguishable in all of its measured physicochemical (melting point, UV and infrared spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08f3e53ba033a16c3a6575dbcb482f1c
https://europepmc.org/articles/PMC175836/
https://europepmc.org/articles/PMC175836/
Autor:
R. F. O. Warren, R. A. Massy-Westropp
Publikováno v:
Chemischer Informationsdienst. 15
The reduction of 1-(furan-2'-yl)nonan-1-one with lithium and ammonia in the presence of alcohols gave 1-(2',3'-dihydrofuran-2'-yl)nonan-1-one as the major product or a mixture of 1-(tetrahydrofuran-2'-yl)nonan-1-one and tridecane-1,5-diol depending o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a21c1da4d574b76899a82b2e714448e6
https://doi.org/10.1002/chin.198443134
https://doi.org/10.1002/chin.198443134
Autor:
R. F. O. Warren, R. A. Massy-Westropp
Publikováno v:
Australian Journal of Chemistry. 37:1303
The reduction of 1-(furan-2'-yl)nonan-1-one with lithium and ammonia in the presence of alcohols gave 1-(2',3'-dihydrofuran-2'-yl)nonan-1-one as the major product or a mixture of 1-(tetrahydrofuran-2'-yl)nonan-1-one and tridecane-1,5-diol depending o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac8c1b8ec4b01dfb550d38ca84cf41b5
https://doi.org/10.1071/ch9841303
https://doi.org/10.1071/ch9841303
Autor:
R. A. Massy-Westropp, R. F. O. Warren
Publikováno v:
Australian Journal of Chemistry. 37:1023
The reductions of 3-(1',1'-ethylenedioxynonyl)furan, 3-(1',1'-dimethoxynonyl)furan, 3-(1'-methoxynonyl)furan and 1-(furan-3'-yl)nonyl acetate with lithium and ammonia are described. The products result from benzylic type cleavage in the absence of an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c0583b1ab4d75b277c1797893d18865
https://doi.org/10.1071/ch9841023
https://doi.org/10.1071/ch9841023
Autor:
R. F. O. Warren, R. A. Massy-Westropp
Publikováno v:
Australian Journal of Chemistry. 37:1969
3-Nonylidenetetrahydrofuran is readily reduced with lithium and ethanol in ammonia to yield mainly 3-nonyltetrahydrofuran together with 3-methyldodecan-1-ol. The reductions of a mixture of 4-nonyl-4,5-dihydrofuran and 3-nonyl-2,Sdihydrofuran and of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6206ed0bf486f93ef558f0cdca12ca74
https://doi.org/10.1071/ch9841969
https://doi.org/10.1071/ch9841969