Zobrazeno 1 - 10
of 80
pro vyhledávání: '"F E, HAHN"'
Publikováno v:
Dalton Transactions. 46:4510-4513
Two new adenine derivatives bearing a N-methylene (1) or N-ethylene (2) tethered diphenylphosphine group have been reacted with [MIIICl2Cp*]2 (M = Ir, Rh) or [RuIIClCp*]4. The formation of Werner-type phosphine complexes [3]–[6] and upon heating th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a76bd6030582fa0805921cf6e84a80e
https://doi.org/10.1039/c7dt00682a
https://doi.org/10.1039/c7dt00682a
Autor:
Roland Fröhlich, Lars Wittenbecher, D. Le Van, Michelle C. Moyes, Ernst-Ulrich Würthwein, T. Von Fehren, F. E. Hahn
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 177:1863-1867
The stable singlet carbenes N,N '-bis(2,2-dimethylpropyl)-benzimidazolin-2-ylidene 1 and 1,3,4,5-tetramethylimidazol-2-ylidene 2 react with phosphaalkynes P L C-- t Bu ( 3a ) or P L C--N i Pr 2 ( 3b ) regioselective to give the aromatic 1,2,4-triphos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::542996f923494bf38ad4ab1195c900ae
https://doi.org/10.1080/10426500212273
https://doi.org/10.1080/10426500212273
Publikováno v:
Dalton Transactions. 46:6129-6129
Correction for ‘Regioselective C8-metalation of N-phosphine tethered adenine derivatives via C8–H activation’ by D. Brackemeyer et al., Dalton Trans., 2017, DOI: 10.1039/c7dt00682a.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22878200c00ad14be8fb31f0a2ef25de
https://doi.org/10.1039/c7dt90068f
https://doi.org/10.1039/c7dt90068f
Publikováno v:
Antibioticschemotherapy (Northfield, Ill.). 9(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c502fd119078fc4539e060016e94ce5
https://pubmed.ncbi.nlm.nih.gov/24545127
https://pubmed.ncbi.nlm.nih.gov/24545127
Publikováno v:
Antibioticschemotherapy (Northfield, Ill.). 4(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94fdfb4fb10913839e9fa8a29db857d2
https://pubmed.ncbi.nlm.nih.gov/24543210
https://pubmed.ncbi.nlm.nih.gov/24543210
Publikováno v:
Antibioticschemotherapy (Northfield, Ill.). 6(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::269a54e1a1cff49ad75ee54e987ad4f9
https://pubmed.ncbi.nlm.nih.gov/24544091
https://pubmed.ncbi.nlm.nih.gov/24544091
Autor:
Birgit Birkmann, F. E. Hahn, Tania Pape, Andreas W. Ehlers, Wolfram W. Seidel, Koop Lammertsma
Publikováno v:
Birkmann, B, Seidel, W W, Pape, T, Ehlers, A W, Lammertsma, K & Hahn, F E 2009, ' Coordination chemistry of the sulfur analog of tricatechol siderophores ', Dalton Transactions, no. 36, pp. 7350-2 . https://doi.org/10.1039/b911014n
Dalton Transactions, 7350-2. Royal Society of Chemistry
ISSUE=36;STARTPAGE=7350;ENDPAGE=2;ISSN=1477-9234;TITLE=Dalton Transactions
Dalton Transactions, 7350-2. Royal Society of Chemistry
ISSUE=36;STARTPAGE=7350;ENDPAGE=2;ISSN=1477-9234;TITLE=Dalton Transactions
Reaction of the siderophore analog tris(benzene-o-dithiol) ligand H6-1 with Ti(OPr)4 in methanol leads to the formation of the siderophore analog complex (Ph4As)2[Ti(1)3] exhibiting exclusively thiolato coordination to the metal center.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1f7634c5befe1d2e020811fcaa2e480
https://hdl.handle.net/1871.1/4118a914-9af6-4e7b-963b-66648e93dd41
https://hdl.handle.net/1871.1/4118a914-9af6-4e7b-963b-66648e93dd41
This volume is the third in the series devoted to Antibiotics initiated by Springer Verlag in 1967. The first two volumes were devoted to the Mode of Action of Antibiotics and Biogenesis, respectively and were received graciously. During the interven
Publikováno v:
Journal of Organometallic Chemistry. 541:51-55
2-Trimethylsiloxyphenyl isocyanide 1 reacts with [MCl2(NCPh)2] (M = Pd, Pt) to yield homoleptic tetraisocyanide complexes [M(1)4]Cl2. Subsequent hydrolysis of the Si-O bonds leads to intramolecular nucleophilic attack at the isocyanide carbon atom wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29c1dc361b79ab9933ab4f67adb13606
https://doi.org/10.1016/s0022-328x(97)00014-4
https://doi.org/10.1016/s0022-328x(97)00014-4