Results 91 to 100 of about 12,716 (277)

Copper‐Catalyzed Enantio‐ and Diastereoselective Addition of Silicon Nucleophiles to 3,3‐Disubstituted Cyclopropenes [PDF]

open access: yes, 2019
A highly stereocontrolled syn‐addition of silicon nucleophiles across cyclopropenes with two different geminal substituents at C3 is reported. Diastereomeric ratios are excellent throughout (d.r.≥98:2) and enantiomeric excesses usually higher than 90 ...
Oestreich, Martin, Zhang, Liangliang
core   +1 more source

Photoinduced Deaminative Borylation of Alkylamines [PDF]

open access: yesJournal of the American Chemical Society, 2018
An operationally simple deaminative borylation reaction of primary alkylamines has been developed. The formation of electron-donor-acceptor complexes between N-alkylpyridinium salts and bis(catecholato)diboron enables photoinduced single-electron transfer and fragmentation to carbon-centered radicals, which are subsequently borylated.
Jingjing Wu   +3 more
openaire   +4 more sources

Spirobifluorene fusion in multiple resonance frameworks enables efficient pure‐red OLEDs with narrowband emission and suppressed efficiency roll‐off

open access: yesFlexMat, EarlyView.
An orthogonal spirobifluorene‐fusion strategy is introduced for B/N/O‐alternated MR frameworks, enabling improved kRISC (5.46 × 103 s−1), high ΦPL (97%), and narrow‐band pure‐red emission. Vacuum‐evaporated OLEDs incorporating this emitter achieve an EQEmax >40% (FWHM = 36 nm) and exhibit exceptionally low efficiency roll‐off at high luminance ...
Yan‐Yun Jing   +7 more
wiley   +1 more source

Postsynthetic modification of zirconium metal-organic frameworks [PDF]

open access: yes, 2016
Metal-organic frameworks (MOFs) have been in the spotlight for a number of years due to their chemical and topological versatility. As MOF research has progressed, highly functionalised materials have become desirable for specific applications, and in ...
Forgan, Ross S., Marshall, Ross J.
core   +1 more source

Heteroatom location‐ and orientation mode‐dependent reverse intersystem crossing rate in multiple resonance emitters

open access: yesFlexMat, EarlyView.
By constructing two pairs of isomers with different heteroatom anchoring positions, the relationship between heteroatom location and orientation mode and reverse intersystem crossing rate constant (kRISC) in multiple resonance (MR) emitters is systematically investigated.
Tingting Huang   +5 more
wiley   +1 more source

Nickel-catalyzed, silyl-directed, ortho-borylation of arenes via an unusual Ni(II)/Ni(IV) catalytic cycle

open access: yesNature Communications
Nickel-catalyzed C–H bond functionalization reactions provide an impressive alternative to those with noble metal catalysts due to their unique reactivity and low cost.
Xiaoshi Su   +6 more
doaj   +1 more source

Iridium-Catalyzed Silylation of Unactivated C-H Bonds. [PDF]

open access: yes, 2019
The functionalization of primary C-H bonds has been a longstanding challenge in catalysis. Our group has developed a series of silylations of primary C-H bonds that occur with site selectivity and diastereoselectivity resulting from an approach to run ...
Hartwig, John F, Romero, Erik A
core  

Tris(pentafluorophenyl)borane and beyond: modern advances in borylation chemistry [PDF]

open access: yes, 2017
As main-group chemistry, in particular boron chemistry, has expanded and developed over the past 20 years, one reagent has risen to prominence as well.
James R. Lawson   +3 more
core   +2 more sources

Preparation of 4,7‐Dihalobenzo[b]Thiophene Derivatives Containing Iodine Atoms and Their Cross Coupling With Arylethynes

open access: yesJournal of Heterocyclic Chemistry, EarlyView.
Quasi T‐shaped three‐way benzo[b]thiophene scaffolds, containing iodine atom(s) at the 4‐ and/or 7‐position, were prepared by several methods such as silica gel‐assisted cyclization. The iodobenzo[b]thiophenes thus prepared were subjected to Sonogashira cross couplings to give various ethynylbenzo[b]thiophenes.
Kozo Toyota   +9 more
wiley   +1 more source

Metal‐Free Electrophilic Borylative Cyclizations of Alkynes

open access: yesThe Chemical Record, EarlyView.
Metal‐free borylative cyclizations based on electrophilic alkyne activation by boron Lewis acids provide efficient access to borylated hetero‐ and carbocycles. Early studies using B(C6F5)3 displayed limited scope and application, whereas recent ClBcat‐ and BCl3‐based methods enable mild CB and CC/CX bond formation for the synthesis of cycles ...
Jaime Mateos‐Gil   +3 more
wiley   +1 more source

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