Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Helena C. Malinakova"'
Autor:
Helena C. Malinakova
Publikováno v:
Journal of Chemical Education. 99:2787-2797
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 51(24)
The synthesis of benzofurans by the reaction of the palladium(II) complex Pd{1-C
Autor:
Helena C. Malinakova
Multicomponent reactions, defined as synthetic protocols that join together three or more substrates in a highly regio- and stereoselective manner to deliver structurally complex organic molecules, have seen a dramatic rise in applications in all fie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f65b22fe31aabc48dc23558cacf7e0c0
https://doi.org/10.1016/b978-0-12-815505-9.00007-x
https://doi.org/10.1016/b978-0-12-815505-9.00007-x
Autor:
Prachi Bangde, Bhalchandra M. Bhanage, Shatrughn A. Bhilare, Pui Ying Choy, Prajakta Dandekar, Ian J.S. Fairlamb, Tejpalsingh R. Girase, Gaurav R. Gupta, Xinwei He, Anant R. Kapdi, Raysa Khan, Fuk Yee Kwong, Fátima Lucio-Martínez, Debabrata Maiti, Helena C. Malinakova, M. Teresa Pereira, Dharmendra Prajapati, Benudhar Punji, Francisco Reigosa, José L. Serrano, Jagrut A. Shah, Kevin H. Shaughnessy, Vineeta Soni, John Spencer, José M. Vila
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::700e827c83a137df59431fc4c50f8fb1
https://doi.org/10.1016/b978-0-12-815505-9.09991-1
https://doi.org/10.1016/b978-0-12-815505-9.09991-1
Publikováno v:
Tetrahedron Letters. 55:4152-4155
A two-step synthesis of rare 2-azabicyclo[2.2.2]octanes is described. N-propargyl amides obtained via Cu(I)-catalyzed three-component coupling, underwent radical-mediated cascade cyclization to afford 5,6-aryl-fused 2-azabicyclo[2.2.2]octanes with ar
Publikováno v:
The Journal of Organic Chemistry. 78:8809-8815
Aryl-fused 2-azabicyclo[2.2.2]octanes were prepared by a novel sequence of Cu-catalyzed three-component coupling of diversely substituted N-benzyl o-bromoaryl imines with methacryloyl chloride and vinyltributyl stannane followed by Pd-catalyzed Heck
Publikováno v:
Synthesis. 44:1983-1992
The synthesis of trisubstituted pyrrolidines and tetrahydrofurans from boronic acids, allenes, and imines or aldehydes via a five- and a three-step protocol, respectively, is described. The assignment of the relative stereochemistry in the pyrrolid
Autor:
Benjamin Neuenswander, Benoy Kumar Pal, Helena C. Malinakova, Sarvesh Kumar, Thomas O. Painter
Publikováno v:
ACS Combinatorial Science. 13:466-477
Parallel solution-phase synthesis of combinatorial libraries of dihydroindenoisoquinolines employing a sequential Cu(I)/Pd(0)-catalyzed multi-component coupling and annulation protocol was realized. The scope and limitations of the protocol with resp
Publikováno v:
Organometallics. 28:810-818
Stable palladapyrrolidinones (L-L)Pd-CH(p-MeC6H4)NBnC(═O)CHPh representing endocyclic carbon-bonded palladium(II) amide enolates with two Pd-bonded sp3-hybridized stereogenic carbons and bidentate ...
Publikováno v:
Journal of Organometallic Chemistry. 693:567-573
Stable pallada(II)cycles featuring Csp 2 –Pd and Csp 3 –Pd bonds reacted with vinyl- and alkynyl(phenyl)iodonium salts to generate two new geminal carbon–carbon bonds to the terminal carbon of the vinyl and alkynyl substituents providing benzof