Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Soren K, Mellerup"'
Autor:
Suning Wang, Soren K. Mellerup, Jiaqi Dong, Nan Wang, Dehui Tan, Lutao Zhang, Jianfeng Wu, Deng-Tao Yang
Publikováno v:
Chemical Communications. 57:9882-9885
A novel and air-stable organo(hydro)diborane featuring a five-membered aryl ring supported bridging B-C-B three-centre-two-electron (3c-2e) bond has been reported. Pyrido[1,2-a]isoindole was found to undergo a stepwise BH3 addition reaction, during w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::740543976f25a4b65919526cc4f8df32
https://doi.org/10.1039/d1cc04228a
https://doi.org/10.1039/d1cc04228a
Autor:
Anselm Herzog, Rüdiger Bertermann, Felipe Fantuzzi, Soren K. Mellerup, Andrea Deißenberger, Holger Braunschweig, Anna Rempel, Bernd Engels
Publikováno v:
Chemistry – A European Journal. 26:16019-16027
Boron tribromide and aryldihaloboranes were found to undergo 1,3-haloboration across one W-N≡N moiety of a group 6 end-on dinitrogen complex (i.e. trans-[W(N2 )2 (dppe)2 ]). The N-borylated products consist of a reduced diazenido unit sandwiched be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1a470eb564fe98b588a1c88e1cb5b32
https://doi.org/10.1002/chem.202002678
https://doi.org/10.1002/chem.202002678
Autor:
Jiali Wen, Bradley M. Vis, Soren K. Mellerup, Stephen D. Kinrade, Roger D. Merchant, Robert C. Mawhinney
Publikováno v:
Journal of the American Chemical Society. 142:9188-9202
A detailed examination of aqueous Si complexation by alditols and aldonic acids was conducted using high-sensitivity 29Si NMR spectroscopy of isotopically enriched solutions combined with theoretic...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2dd0824b41f6c012848d8eec0761718
https://doi.org/10.1021/jacs.9b10701
https://doi.org/10.1021/jacs.9b10701
Autor:
Soren K. Mellerup, Suning Wang
Publikováno v:
PATAI'S Chemistry of Functional Groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f22a93d9a0d5ca693e99518dc0f1d0d0
https://doi.org/10.1002/9780470682531.pat0974
https://doi.org/10.1002/9780470682531.pat0974
Autor:
Jiaqi, Dong, Lutao, Zhang, Dehui, Tan, Jianfeng, Wu, Nan, Wang, Soren K, Mellerup, Suning, Wang, Deng-Tao, Yang
Publikováno v:
Chemical communications (Cambridge, England). 57(77)
A novel and air-stable organo(hydro)diborane featuring a five-membered aryl ring supported bridging B-C-B three-centre-two-electron (3c-2e) bond has been reported. Pyrido[1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4cea396fc7bcb1330c6961c9ff5a801b
https://pubmed.ncbi.nlm.nih.gov/34494050
https://pubmed.ncbi.nlm.nih.gov/34494050
Publikováno v:
Angewandte Chemie. 131:6755-6759
B(npy)Ar2 (npy=2-(naphthalen-1-yl)pyridine) compounds bearing various nonbulky aryl groups undergo a clean and sequential two-step photoisomerization in which two aryl substituents on boron migrate to a carbon atom of the naphthyl moiety. The second
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbc5c3bb6f233264e9e83bad5bac119e
https://doi.org/10.1002/ange.201902231
https://doi.org/10.1002/ange.201902231
Autor:
Soren K. Mellerup, Suning Wang
Publikováno v:
Trends in Chemistry. 1:77-89
Boron-containing π-conjugated systems are an emerging class of materials for important energy-conversion applications. Because of its electron-deficient nature, embedding boron atoms into an organic material introduces electron-accepting centers tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c607e3c759f230e06bb34a13e9312ca2
https://doi.org/10.1016/j.trechm.2019.01.003
https://doi.org/10.1016/j.trechm.2019.01.003
Publikováno v:
Organic Letters. 21:2838-2842
Alkylamino-functionalized donor-π-acceptor (D-π-A) triarylboranes have been found to be able to capture CO2, forming the carbamic acid derivative. Due to the close proximity of the amine substituent to the boron center, CO2 binding greatly influenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d3aeebebb6785d0042d681cfc007ebd
https://doi.org/10.1021/acs.orglett.9b00831
https://doi.org/10.1021/acs.orglett.9b00831
Publikováno v:
Tetrahedron. 75:809-816
Several examples of laterally appended donor-π-acceptor (D-π-A) boron compounds based on a biphenyl unit have been synthesized and fully characterized. Intramolecular H bonds or n-π* interactions have been found to have a great impact on the photo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e83d3640970242081aa2de297f1b2bf1
https://doi.org/10.1016/j.tet.2018.12.032
https://doi.org/10.1016/j.tet.2018.12.032
Autor:
Anna, Rempel, Soren K, Mellerup, Felipe, Fantuzzi, Anselm, Herzog, Andrea, Deißenberger, Rüdiger, Bertermann, Bernd, Engels, Holger, Braunschweig
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Boron tribromide and aryldihaloboranes were found to undergo 1,3‐haloboration across one W−N≡N moiety of a group 6 end‐on dinitrogen complex (i.e. trans‐[W(N2)2(dppe)2]). The N‐borylated products consist of a reduced diazenido unit sandwi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aee790a03cb9c5ef02068278d1405fc3
https://pubmed.ncbi.nlm.nih.gov/32957161
https://pubmed.ncbi.nlm.nih.gov/32957161