Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Bruce R, Whittlesey"'
Autor:
George N. Harakas, Bruce R. Whittlesey
Publikováno v:
IUCrData, Vol 6, Iss 8, p x210845 (2021)
The reaction of Na2Fe(CO)4 with an excess of MnCl2 in tetrahydrofuran (THF) produced {Fe2Mn(C4H8O)2Na2(C4H8O)5(CO)8]n or C36H56Fe2MnNa2O15. The compound is a xenophilic dianion with short iron–manganese bond lengths of 2.6274 (10) and 2.6294 (10)
Externí odkaz:
https://doaj.org/article/9a3d433736c5462a9219259cca6faa38
Autor:
Abdelaaty A. Shahat, Bruce R. Whittlesey, Paul W. Paré, Fathy F. Abdel-Latif, Tarik A. Mohamed, Mohamed-Elamir F. Hegazy, Amira M. Gamal Eldeen
Publikováno v:
Marine Drugs, Vol 10, Iss 1, Pp 209-222 (2012)
A chemical investigation of an ethyl acetate extract of the Red Sea soft coral Sarcophyton glaucum has led to the isolation of two peroxide diterpenes, 11(S) hydroperoxylsarcoph-12(20)-ene (1), and 12(S)-hydroperoxylsarcoph-10-ene (2), as well as 8-e
Externí odkaz:
https://doaj.org/article/c31b2f8646ff42d5b2c3cc73692b6eb3
Publikováno v:
ARKIVOC, Vol 2010, Iss 7, Pp 65-80 (2010)
Externí odkaz:
https://doaj.org/article/562036a73e804aba9d7274b2805638a1
Autor:
Bruce R. Whittlesey, George N. Harakas
Publikováno v:
IUCrData, Vol 6, Iss 8, p x210845 (2021)
The reaction of Na2Fe(CO)4 with an excess of MnCl2 in tetrahydrofuran (THF) produced {Fe2Mn(C4H8O)2Na2(C4H8O)5(CO)8] n or C36H56Fe2MnNa2O15. The compound is a xenophilic dianion with short iron–manganese bond lengths of 2.6274 (10) and 2.6294 (10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcfd42ea461ba45e2a284b6087cc0411
https://doi.org/10.1107/s2414314621008452
https://doi.org/10.1107/s2414314621008452
Autor:
George N, Harakas, Bruce R, Whittlesey
Publikováno v:
IUCrData. 6(Pt 8)
The reaction of Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0742a4943849d7e0bb3651f4aa3645e
https://pubmed.ncbi.nlm.nih.gov/36339454
https://pubmed.ncbi.nlm.nih.gov/36339454
Publikováno v:
European Journal of Inorganic Chemistry. 2011:1699-1702
The pyrazolyl-functionalized oligosilanes Si(SiMe2PzR)4 (2a R = tBu; 2b R = iPr) were prepared by the reaction of 3-R-pyrazole (R = iPr, tBu) with Si(SiMe2Cl)4 in the presence of NEt3. By treatment with tBuOK and 18-crown-6 in THF, 2a, b were convert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7d619e64ea433409109688111de23f1
https://doi.org/10.1002/ejic.201001291
https://doi.org/10.1002/ejic.201001291
Publikováno v:
ARKIVOC, Vol 2010, Iss 7, Pp 65-80 (2010)
Optically active aziridines were synthesized from the reaction of chiral nonracemic N-tert-butanesulfinyl imines with benzyl-stabilized sulfur ylides, wherein the latter were generated from a rhodium-catalyzed decomposition of phenyldiazomethane (PDM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53b1ec86622435bbd5aea7b858108c44
https://doi.org/10.3998/ark.5550190.0011.706
https://doi.org/10.3998/ark.5550190.0011.706
Publikováno v:
Tetrahedron Letters. 50:6064-6067
The viologen N,N′-dicyanomethyl-4,4′-bipyridinium·2PF6 was found to induce an aza-Diels–Alder reaction of N-arylimines with N-vinylpyrrolidinone or N-vinylcarbazole, producing tetrahydroquinoline derivatives with high cis/trans selectivities a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7276dc53726d699c9c35ca21ac3d3f6
https://doi.org/10.1016/j.tetlet.2009.08.058
https://doi.org/10.1016/j.tetlet.2009.08.058
Publikováno v:
ChemInform. 46
A variety of aliphatic and aromatic aldehydes and ketones are selectively reduced under mild conditions using a monomeric aluminum complex as the catalyst.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33703dc7b01977bc75e954158b446989
https://doi.org/10.1002/chin.201517092
https://doi.org/10.1002/chin.201517092
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 20(46)
The metal-catalyzed Meerwein-Ponndorf-Verley (MPV) reduction allows for the mild and sustainable reduction of aldehydes and ketones but has not found widespread application in organic synthesis due to the high catalyst loading often required to obtai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b4e5cb6bb45ee7a8f4d5d8c02ba3a1a
https://pubmed.ncbi.nlm.nih.gov/25284749
https://pubmed.ncbi.nlm.nih.gov/25284749