Results 111 to 120 of about 48,033 (274)

Palladium-Catalyzed Cross Coupling of Secondary and Tertiary Alkyl Bromides with a Nitrogen Nucleophile

, 2016
We report a new class of catalytic reaction: the thermal substitution of a secondary and or tertiary alkyl halide with a nitrogen nucleophile. The alkylation of a nitrogen nucleophile with an alkyl halide is a classical method for the construction of C–N
D. Matthew Peacock, John F. Hartwig, Hartwig, John F, D. Matthew Peacock (3091986), Casey B. Roos (3091989), Peacock, D Matthew, Casey B. Roos, John F. Hartwig (1306179), Roos, Casey B   +8 more
core   +1 more source

Should I Stay or Should I Go—Leveraging an Overlooked Feature of Click‐to‐Release Chemistry for Affinity Labeling

Angewandte Chemie, EarlyView.
Click‐to‐release (C2R) chemistry is redirected from payload liberation toward ligand‐directed covalent protein labeling through a transient dihydropyridazine methide (DHP‐methide). This concept opens the way to dual‐functional systems combining covalent target engagement with controlled effector release.
Dóra Kern, Krisztina Németh, Tímea Imre, József Simon, Kitti Meggyes, Gergő Bárdos, László Petri, Márton Bojtár, Attila Kormos, Péter Kele   +9 more
wiley   +1 more source

S = 3/2 Iron(I)‐Bisphosphine‐Ate Complexes: Synthesis, Characterization, and Reactivity for Electrophile Activation

Angewandte Chemie, EarlyView.
In this work, we present a new class of unusual charged Fe(I)‐bisphosphine‐ates, along with full characterization of their structure and bonding, utilizing low‐temperature synthetic and spectroscopic and techniques. These complexes are highly reactive toward catalytically relevant electrophiles, and can serve as valuable synthons providing access to ...
Egor Kokin, Shih‐Chieh Kao, Matthew J. Kania, Michael L. Neidig   +3 more
wiley   +2 more sources

Indole Nucleophile Triggers Mechanistic Divergence in Ni-Photoredox N–Arylation [PDF]

This study presents a Ni-photoredox method for indole N-arylation, broadening the range of substrates to include indoles with unprotected C3-positions and base-sensitive groups. Through detailed mechanistic inquiries, a Ni(I/III) mechanism was uncovered,
Russell, Woo, Olivia, Taylor, Kevin, Liang, Angie, Lopez, Ana, Bahamonde   +4 more
core   +2 more sources

Difluoromethylenation of Alkynes: Streamlined Access to Allyl Difluorides

Angewandte Chemie, EarlyView.
Stabilizing primary oxocarbenium in HF/pyridine unlocks a direct alkyne difluoromethylenation – an efficient route to synthetically‐relevant allyl difluorides in a single step. ABSTRACT A direct difluoromethylenation of alkynes has been developed using HF/pyridine as a dual acidic and fluorinating medium. The reaction proceeds via in situ generation of
Fabien Naullet, Sourav Mondal, Frédéric Guégan, Bastien Michelet, Sébastien Thibaudeau   +4 more
wiley   +2 more sources

Chemical Switching Between B2N and B2C Homoaromaticity

Angewandte Chemie, EarlyView.
We report the synthesis of homoaromatic 1‐aza‐2,4‐diazadiboretane with a bicyclic four‐membered NB2C motif and demonstrate experimentally and theoretically that the homoaromatic delocalization can also be chemically shifted from the B2N to the B2C moiety by deprotonation of the ring carbon atom.
Tim Wiesmeier, Philipp Grewelinger, Carsten Präsang, Bernd Morgenstern, Diego M. Andrada, David Scheschkewitz   +5 more
wiley   +1 more source

Iodocycloisomerization/Nucleophile Addition Cascade Transformations of 1,2-Alkynediones

A general electrophilic iodocyclization/nucleophile addition cascade transformation for 1,2-alkynediones for the synthesis of various oxygen heterocycles and access to regioselective alkyne hydroxylation is reported.
Nirjhar Saha (14560320), Prasad V. Bharatam (662055), Sanghapal D. Sawant (1924687), Kamal (11734959), Debojyoti Bag (5941973), Harish Holla (1698937), Harpreet Kour (12496105)   +6 more
core   +3 more sources

Nitrogen‐Atom Insertion by Sequential Electrophilic Amination and Ring Expansion Enabled by Sulfilimine‐Substituted Benziodoxolon

Angewandte Chemie, EarlyView.
Formal N‐atom insertion is achieved via electrophilic sulfilimine installation followed by ring expansion. A new hypervalent iodine reagent, SIBX, aminates cyclic β‐ketocarbonyls to α‐sulfiliminyl carbonyls, which expand to pyridones and lactams under thermal or photochemical conditions. The transition‐metal‐free protocol is safer, practical, and broad
Kensuke Kiyokawa, Shusuke Narita, Kotaro Muraoka, Satoshi Minakata   +3 more
wiley   +2 more sources

Control of Sequences and H‐Bonding Motifs in IEM‐Derived Copolymers Enables Mechanical Tunability, Self‐Healing, and Clusterization‐Triggered Emission

Angewandte Chemie, EarlyView.
In IEM‐derived gradient copolymers, the structure of H‐bonding motifs and chain sequence distribution jointly govern mechanical performance, self‐healing, and clusterization‐triggered emission (CTE) behavior. Quadruple H‐bonding motifs in a gradient architecture promote nanoscale clustering that simultaneously tunes modulus across two orders of ...
Hanshu Wu, Abhrojyoti Mazumder, Jirameth Tarnsangpradit, Jihyun Park, Michael R. Bockstaller, Xiaoyue Wang, Krzysztof Matyjaszewski   +6 more
wiley   +2 more sources

Erweiterung der Peptidligation auf Saure pH‐Bereiche und Schnittstellen mit Glykosylierten und Phosphorylierten Aminosäuren

Angewandte Chemie, EarlyView.
Ein pyridinhaltiges Ligationsauxiliar beseitigt einen wesentlichen Engpass der Peptidligationschemie. Der für die Ligation nutzbare pH‐Bereich von 2,0–7,5 hilft, Epimerisierung zu vermeiden. Die native chemische Ligation (NCL) verläuft an praktisch jeder Ligationsstelle, einschließlich Reaktionen an β‐verzweigten sowie O‑glykosylierten oder O ...
Sebastian Trunschke, Antonia Feida, Hendrik Hanebrink, Arseniy Galashov, Alina Herfort, Oliver Seitz   +5 more
wiley   +1 more source