Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Abigail L. Smenton"'
Autor:
Charli M. Long, Marisa C. Buzzeo, Sahar A. Saddoughi, Sonal Patel, Linda H. Doerrer, John F. C. Turner, and Arnold L. Rheingold, David Millar, Amber H. Iqbal, Richard G. Compton, Abigail L. Smenton, Jay D. Wadhawan, Matthew A. Pellow, James A. Golen
Two series of homoleptic phenolate complexes with fluorinated aryloxide ligands A2[M(OAr)4] with M = Co2+ or Cu 2+, OAr- = (OC6F5)- (OArF) or {3,5-OC6H3(CF3) 2}- (OAr′), A+ = K (18-crown-6) +, Tl+, Ph4P+, Et3HN +, or Me4N+ have been synthesized. Tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9311e27a6c61a8786888fbb1d4138675
https://ora.ox.ac.uk/objects/uuid:124385bb-52f0-4afc-9176-f9c584410e57
https://ora.ox.ac.uk/objects/uuid:124385bb-52f0-4afc-9176-f9c584410e57
Autor:
Sarah E. Bernard, Shenjuti Chowdhury, Nadia C. Abascal, Elsy Santizo-Deleon, Christian M. Rojas, Abigail L. Smenton, Ritu Gupta, Lindsay M. Repka, Victoria Baranov, Brisa Hurlocker
Publikováno v:
The Journal of Organic Chemistry. 76:2240-2244
By using (N-tosyloxy)-3-O-carbamoyl-D-glucal 10, which removes the need for a hypervalent iodine(III) oxidant, we provide evidence for rhodium nitrenoid-mediated ipso C-H activation as the origin of a C3-oxidized dihydropyranone product 3. This syste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57fa9d469563a7e5988b7b5671ae4552
https://doi.org/10.1021/jo101599q
https://doi.org/10.1021/jo101599q
Autor:
Bridget K. Marcellino, Alexandra Severino, Rena Bodner, Christian M. Rojas, and Abigail L. Smenton
Publikováno v:
The Journal of Organic Chemistry. 70:3988-3996
[reaction: see text] Glucal 3-carbamates 1 and 7 underwent oxidative cyclization with iodobenzene diacetate or iodosobenzene in the presence of Rh2(OAc)4, providing mannosamine 2-N,3-O-oxazolidinones. With iodosobenzene, incorporation of 4-penten-1-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10036bee357c39d2d5db908ff984651e
https://doi.org/10.1021/jo0500129
https://doi.org/10.1021/jo0500129