Zobrazeno 1 - 10
of 37
pro vyhledávání: '"R. A. Massy-Westropp"'
Autor:
L. M. Tippett, R. A. Massy‐Westropp
Publikováno v:
ChemInform. 24
The stereoselectivity of reduction of 4-substituted 1-methylene-1,2,3,4-tetrahydronaphthalenes has been investigated by using catalytic hydrogenation and lithium in ammonia solutions. Serrulatane derivatives underwent highly stereoselective catalytic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7724b77f5360f37e368226ffacaa756c
https://doi.org/10.1002/chin.199338289
https://doi.org/10.1002/chin.199338289
Publikováno v:
Zeitschrift für Kristallographie - Crystalline Materials. 198:151-154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e351df85f2f4760f05d57a05e76ecb9
https://doi.org/10.1524/zkri.1992.198.14.151
https://doi.org/10.1524/zkri.1992.198.14.151
Publikováno v:
Zeitschrift für Kristallographie. 198:151-154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0d2ab7ba013c7b25be7b74286aee13e
https://doi.org/10.1524/zkri.1992.198.1-2.151
https://doi.org/10.1524/zkri.1992.198.1-2.151
Autor:
L. M. Tippett, R. A. Massy‐Westropp
Publikováno v:
Australian Journal of Chemistry. 46:945
The stereoselectivity of reduction of 4-substituted 1-methylene-1,2,3,4-tetrahydronaphthalenes has been investigated by using catalytic hydrogenation and lithium in ammonia solutions. Serrulatane derivatives underwent highly stereoselective catalytic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd4b18f2f1baf69a5d9bf4362bb8321c
https://doi.org/10.1071/ch9930945
https://doi.org/10.1071/ch9930945
Publikováno v:
Journal of the American Chemical Society. 84:3732-3736
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12964b465e97fe11b4167af1d6df5301
https://doi.org/10.1021/ja00878a027
https://doi.org/10.1021/ja00878a027
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:
E. Dimitriadis, R. A. Massy-Westropp
Publikováno v:
Chemischer Informationsdienst. 12
Two new furanosesquiterpenes, 7-methyl-7-(4'-methylpenta-1',3'-dienyl)- 4,5,6,7-tetrahydrobenzofuran and 4-hydroxydendrolasin [(S,E)-9-(furan- 3'-yl)-2,6-dimethylnona-2,6-dien-4-ol], are described. The structure of the former compound was confirmed b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac5be6430181a9dbc0bb1e5e174322a9
https://doi.org/10.1002/chin.198116313
https://doi.org/10.1002/chin.198116313
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
Autor:
M. F. Price, R. A. Massy-Westropp
Publikováno v:
Chemischer Informationsdienst. 11
The 5-oxo-2,5-dihydrofuran-2-ylideneacetic acids (2a), (3a), (9a), (10a), (11a), (12a) and (13a) have been synthesized by a procedure which allows the unambiguous assignment of the stereochemistry about the double bond in each isomer. The method, of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89ae56c4529700b0c79e1ffb9bcd7431
https://doi.org/10.1002/chin.198042146
https://doi.org/10.1002/chin.198042146