Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Suman, Dana"'
Publikováno v:
Organic Letters. 25:70-75
An enol-assisted regioselective arene C-H alkylation with maleimides is developed under redox-neutral ruthenium(II) catalysis, offering a wide variety of valuable 3-aryl succinimides including amino acid embedded frameworks in good to excellent yield
Publikováno v:
Organic Letters. 24:9228-9232
Autor:
Suman Dana, Mahiuddin Baidya
Publikováno v:
Handbook of CH‐Functionalization. :1-53
Despite the significant progress in enantioselective catalysis during the past decades, asymmetric redox transformations typically rely on costly transition metals as catalysts, along with the use of stoichiometric amounts of chemical redox agents. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b11103206ae8681c1d98a6b919880c6a
https://doi.org/10.26434/chemrxiv-2023-dzw3d
https://doi.org/10.26434/chemrxiv-2023-dzw3d
Publikováno v:
Organic letters. 24(50)
The hydrocarbofunctionalization of allyl amines connected to the picolinamide directing group is developed under Pd(II) catalysis. The strategy is grounded on a nucleopalladation concept, and a wide range of indoles effectively participated to produc
Publikováno v:
Organic Letters. 23:6855-6860
A Ru(II)-catalyzed cross-dehydrogenative Heck-type olefination of arenes with allyl sulfones leveraging the assistance of weakly coordinating ketone and amide functional groups is reported. It features a distinct reactivity profile in comparison to o
Publikováno v:
The Chemical Record. 21:3795-3817
Transition-metal-catalyzed direct transformation of inert C-H bond has revolutionized the arsenal of main-stream organic synthesis, providing a new upfront to forge structurally enriched and biologically relevant scaffolds in a step- and atom-economi
Publikováno v:
Chemistry, an Asian journal. 17(23)
Ru(II)-catalyzed C-H bond activation strategy has been capitalized through a (4+2) annulative difunctionalization of non-conjugated alkenyl amides. Under mild conditions, a broad range of (hetero)aromatic amides embedded with NH-OMe unit as an intern
Publikováno v:
Current Opinion in Electrochemistry. :101312
Publikováno v:
European Journal of Organic Chemistry. 2021:1385-1389