Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Christian M. Rojas"'
Autor:
Marina Orman, Maya Landis, Aisha Oza, Deepika Nambiar, Joana Gjeci, Kristen Song, Vivian Huang, Amanda Klestzick, Carla Hachicho, Su Qing Liu, Judith M. Kamm, Francesca Bartolini, Jean J. Vadakkan, Christian M. Rojas, Christina L. Vizcarra
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract SMIFH2 is a small molecule inhibitor of the formin family of cytoskeletal regulators that was originally identified in a screen for suppression of actin polymerization induced by the mouse formin Diaphanous 1 (mDia1). Despite widespread use
Externí odkaz:
https://doaj.org/article/22ce7b7289964ffe9f607b0046be54e2
Autor:
Marina Orman, Maya Landis, Aisha Oza, Deepika Nambiar, Joana Gjeci, Kristen Song, Vivian Huang, Amanda Klestzick, Carla Hachicho, Su Qing Liu, Judith M. Kamm, Francesca Bartolini, Jean J. Vadakkan, Christian M. Rojas, Christina L. Vizcarra
SMIFH2 is a small molecule inhibitor of the formin family of cytoskeletal regulators that was originally identified in a screen for suppression of actin polymerization induced by the mouse formin Diaphanous 1 (mDia1). Despite widespread use of this c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebd81ae85c8bb385883d2f80c8e2226f
https://doi.org/10.1101/2022.03.10.483826
https://doi.org/10.1101/2022.03.10.483826
Autor:
Christian M. Rojas
Designed for practitioners of organic synthesis, this book helps chemists understand and take advantage of rearrangement reactions to enhance the synthesis of useful chemical compounds. Provides ready access to the genesis, mechanisms, and synthetic
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
Publikováno v:
Organic Letters. 11:1527-1530
In the Rh(2)(OAc)(4)-catalyzed amidoglycosylation of glucal 3-carbamates, anomeric stereoselectivity and the extent of competing C3-H oxidation depend on the 4O and 6O protecting groups. Acyclic protection permits high alpha-anomer selectivity with f
Autor:
Christian M. Rojas
Publikováno v:
Molecular Rearrangements in Organic Synthesis: Rojas/Molecular Rearrangements in Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::691a00ac9e9ece5b5c29124291e67d1c
https://doi.org/10.1002/9781118939901
https://doi.org/10.1002/9781118939901
Autor:
Christian M. Rojas
Publikováno v:
Molecular Rearrangements in Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9883f40d2ca29fbd39c4294d020a4cd
https://doi.org/10.1002/9781118939901.ch18
https://doi.org/10.1002/9781118939901.ch18
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
Autor:
David G. Churchill, Christian M. Rojas
Publikováno v:
Tetrahedron Letters. 43:7225-7228
Iron(II) halides promoted intramolecular alkene amidation in a C3–allal azidoformate. In the presence of alcohols, one-pot β-glycosylation followed. Without added alcohol, amidochlorination occurred using FeCl2, providing an anomeric mixture of gl
Autor:
Cindy Kan, Charli M. Long, Sarah E. Tully, Moushumi Paul, Christian M. Rojas, Christina M. Ring
Publikováno v:
Organic Letters. 3:381-384
[figure: see text] Photolysis of an allal C-3 azidoformate provoked intramolecular nitrene insertion into the glycal C=C unit and allowed direct incorporation of alcohol nucleophiles as beta-disposed substituents at C-1. The 2-amido allopyranoside pr