Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Johannes Kloesges"'
Autor:
Johannes Klösges
Das kirchliche Prozessrecht manifestiert sich in einem detailreichen Normenkomplex, der nur selten in den Blick wissenschaftlicher Untersuchung gerät. Grund genug, einigen Detailfragen Raum zu geben, die gleichzeitig paradigmatische Problemanzeigen
Autor:
Johannes Klösges
Die Zahl der Ehenichtigkeitsverfahren, die an deutschen Diözesangerichten mit einer Streitfrage aus einer der drei psychischen Eheunfähigkeiten des c. 1095 CIC geführt werden, ist in den vergangenen Jahren kontinuierlich gestiegen und macht nun fa
Autor:
Barbara Odell, Ilya Kuprov, Christopher I. Pearson, Johannes Kloesges, Timothy D. W. Claridge, David M. Hodgson
Publikováno v:
Angewandte Chemie (International Ed. in English)
Anomalous NOESY cross-peaks that cannot be explained by dipolar cross-relaxation or chemical exchange are described for carbon-substituted aziridines. The origin of these is identified as scalar cross-relaxation of the first kind, as demonstrated by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e23d493779bd5809cfcc0b532334b12
https://ora.ox.ac.uk/objects/uuid:d0cd1a8f-6d1c-4304-a93f-7211d244ad11
https://ora.ox.ac.uk/objects/uuid:d0cd1a8f-6d1c-4304-a93f-7211d244ad11
Autor:
David M. Hodgson, Johannes Kloesges
The fourth protocol: the rarely studied N-thiopivaloyl group plays a crucial role in mediating efficient α lithiation and incorporation of diverse electrophiles onto an azetidine ring; in the presence of chiral ligands, this chemistry also provides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ed8868985dc1a09b925cea7983da035
https://ora.ox.ac.uk/objects/uuid:2cc7b82f-084c-45f0-bab8-bd63f56bbd74
https://ora.ox.ac.uk/objects/uuid:2cc7b82f-084c-45f0-bab8-bd63f56bbd74
Publikováno v:
Angewandte Chemie. 122:7952-7956
Autor:
Deepshikha Angrish, Caroline H. Lee, David M. Hodgson, Stephanie P. Erickson, Johannes Kloesges
Publikováno v:
Organic Letters. 10:5553-5556
Alpha-diazo-beta-ketoesters bearing allylic ether functionality undergo highly stereoselective Ru-carbene-catalyzed alkene cross-metathesis followed by Rh(2)(OAc)(4)-catalyzed oxonium ylide formation/[2,3] sigmatropic rearrangement in a one-flask ope
Publikováno v:
Angewandte Chemie (International ed. in English). 49(42)
Autor:
Johannes Kloesges, David M. Hodgson
Publikováno v:
ChemInform. 41
The fourth protocol: the rarely studied N-thiopivaloyl group plays a crucial role in mediating efficient α lithiation and incorporation of diverse electrophiles onto an azetidine ring; in the presence of chiral ligands, this chemistry also provides
Publikováno v:
ChemInform. 40
Autor:
Deepshikha Angrish, Stephanie P. Erickson, David M. Hodgson, Johannes Kloesges, Caroline H. Lee
Publikováno v:
ChemInform. 40
Alpha-diazo-beta-ketoesters bearing allylic ether functionality undergo highly stereoselective Ru-carbene-catalyzed alkene cross-metathesis followed by Rh(2)(OAc)(4)-catalyzed oxonium ylide formation/[2,3] sigmatropic rearrangement in a one-flask ope