Results 161 to 170 of about 30,672 (247)

Enantioselective Benzylic C-H Insertions with Diazosuccinate Esters. [PDF]

Org Lett
Kamuti NM, Bagale B, Bunge SD, Ndakala AJ, Mighion JD.   +4 more
europepmc   +1 more source

Silylium-Ion-Initiated Disulfidation of Unactivated Alkenes with Disulfides: Methodology and Isolation of the Sulfenium-Ion Carriers. [PDF]

J Org Chem
Xu B, Liu X, Morgan DM, Irran E, Oestreich M.   +4 more
europepmc   +1 more source

Strategies towards designing visible and near-infrared light driven molecular motors.

Chem Soc Rev
Tu Y, Danowski W, Stindt CN, Sheng J, Feringa BL.   +4 more
europepmc   +1 more source

PhSO₂CF₂H as a difluoromethylene bridge connecting electrophiles and electronically diverse alkenes. [PDF]

Chem Sci
Zhao Y, Zhu K, Zhao F, Zhang Y, Ni C, Hu J.   +5 more
europepmc   +1 more source

Gold Single‐Atom Catalysts Enable Selective Shuttle Hydrochlorination of Alkynes

Angewandte Chemie International Edition, EarlyView.
Gold single‐atom catalysts on activated carbon enable heterogeneous shuttle hydrochlorination of terminal alkynes to vinyl chlorides with high chemo‐ and stereo‐selectivity thanks to cooperation between Au(I) sites and the support. The catalytic system combines broad substrate compatibility, simplified separation, and recoverability, paving the way for
Marc‐Eduard Usteri, Eva J. Meeus, Christian Zachau, Seung‐Eun Choi, Aram Bugaev, Milivoj Plodinec, Sharon Mitchell, Bill Morandi, Javier Pérez‐Ramírez   +8 more
wiley   +1 more source

Synergistic effects in s- and d-block heterometallic compounds: small molecule activation and catalysis. [PDF]

Chem Sci
Gawron M, Wolf R.
europepmc   +1 more source

Nickel-catalyzed hydro- and deuteroacylation of acrylates using water as the hydrogen source. [PDF]

Chem Sci
Lindenmaier IH, Bölzle F, Fleischer I.
europepmc   +1 more source

Photochemical Hetero-cycloadditions. [PDF]

Chem Rev
Rosso C, Corti V, Goti G, Cuadros S, Marcantonio E, Dell'Amico L.   +5 more
europepmc   +1 more source

Aza‐Büchner–Curtius–Schlotterbeck Reaction Enables Selective Construction of Quaternary Carbon Centers

Angewandte Chemie International Edition, EarlyView.
We introduce the Aza‐Büchner–Curtius–Schlotterbeck (ABCS) reaction: A mild, catalyst‐free method for homologating aryl imines. Diverging from the traditional BCS mechanism, the diazo intermediate undergoes selective C─C insertion to form an all‐carbon quaternary center.
Simon O. Angerer, Vincent George, Aryaman Pattanik, Gaia Carpentiero, Tereza Morcinková, Julia Rehbein, Burkhard König   +6 more
wiley   +1 more source

Isolable C-Phosphonio-Boratavinyl Anion. [PDF]

Angew Chem Int Ed Engl
Xu H, Rodríguez-Álvarez A, Hossain MJ, Baceiredo A, Maerten E, Saffon-Merceron N, Branchadell V, Kato T.   +7 more
europepmc   +1 more source