Zobrazeno 1 - 10
of 38
pro vyhledávání: '"G. Kneer"'
Publikováno v:
Animal, Vol 7, Iss 7, Pp 1119-1127 (2013)
In this study, 10 samples of rapeseed meal (RSM) from 10 different oil plants in Germany were examined. In situ rumen degradation of CP was determined by incubation over 1, 2, 4, 8, 16, 32 and 72 h in duplicate per time point using three rumen fistul
Externí odkaz:
https://doaj.org/article/22c876d3754542859baa494495743d6b
Publikováno v:
Technikfolgenabschätzung – Theorie und Praxis, Vol 9, Iss 2 (2000)
Externí odkaz:
https://doaj.org/article/4870fd98a1974162b63895b59c789c0e
Publikováno v:
Animal, Vol 7, Iss 7, Pp 1119-1127 (2013)
In this study, 10 samples of rapeseed meal (RSM) from 10 different oil plants in Germany were examined. In situ rumen degradation of CP was determined by incubation over 1, 2, 4, 8, 16, 32 and 72 h in duplicate per time point using three rumen fistul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14ab91bfb224dbc2e3f64a3f43f1c108
http://www.sciencedirect.com/science/article/pii/S175173111300030X
http://www.sciencedirect.com/science/article/pii/S175173111300030X
Cesa/Vasa: neue Operationsverfahren zur Behandlung der Drang- und Mischinkontinenz und des Deszensus
Publikováno v:
Geburtshilfe und Frauenheilkunde. 74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3b6fd69d53ef22486d23022eb86e906
https://doi.org/10.1055/s-0034-1388272
https://doi.org/10.1055/s-0034-1388272
Autor:
Jochen Mattay, G. Kneer
Publikováno v:
ChemInform. 24
Moderate facial selectivities are observed in additions of alkyl radicals to the chiral (c,d) olefin (2 S )-2- tert -butyl-5-ethoxycarbonylmethylene-1,3-dioxolane-4-one 1 . The following hydrogen abstraction from tributylstannane proceeds with excell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04bd6a9c2c3db348a6075251b5dcdb5b
https://doi.org/10.1002/chin.199326124
https://doi.org/10.1002/chin.199326124
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d015af6651c1563a0aa77c50cf6d426a
https://doi.org/10.1002/chin.199531039
https://doi.org/10.1002/chin.199531039
Autor:
Jochen Mattay, G. Kneer
Publikováno v:
Tetrahedron Letters. 33:8051-8054
Moderate facial selectivities are observed in additions of alkyl radicals to the chiral (c,d) olefin (2 S )-2- tert -butyl-5-ethoxycarbonylmethylene-1,3-dioxolane-4-one 1 . The following hydrogen abstraction from tributylstannane proceeds with excell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::136066eda00a6dc1857edb4f7f94ee09
https://doi.org/10.1016/s0040-4039(00)74714-9
https://doi.org/10.1016/s0040-4039(00)74714-9
Publikováno v:
Synthesis. 1990:599-603
The synthesis of title chiral olefin (I)is described. Its structure is determined by X-ray analysis. The Diels-Alder reaction of I with cyclopentadiene exclusively yields the exo products with a face selectivity up to 95 %
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef2b51c6790eb6326b5d0d0ff9be6b2e
https://doi.org/10.1055/s-1990-26955
https://doi.org/10.1055/s-1990-26955
Publikováno v:
Synlett. 1990:145-147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0933e150b3ba83f9a6a91fce37cad56b
https://doi.org/10.1055/s-1990-21014
https://doi.org/10.1055/s-1990-21014
The hydrogen abstraction of radical intermediates yielded by radical addition to the methylene compound 6, shows excellent facial selectivity. Conformational analyses of the radical intermediates were carried out by quantum chemical calculations and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d77e9e955540d65d6fbbd75a18b7de54
https://pub.uni-bielefeld.de/record/2402682
https://pub.uni-bielefeld.de/record/2402682
