Results 261 to 270 of about 538,570 (408)

Influence of a Two-Fold Ligation Pattern on Iron-Mediated Aryl-Heteroaryl Cross-Electrophile Couplings. [PDF]

JACS Au
Djebbar F, Chamoreau LM, Lefèvre G.
europepmc   +1 more source

THE HISTOCHEMICAL REACTION OF ARYL AMINES WITH TISSUE ALDEHYDES PRODUCED BY PERIODIC AND CHROMIC ACIDS

, 1962
R. D. Lillie
openalex   +1 more source

INTERACTION OF ARYL-SUBSTITUTED THIURETS AND AROMATIC AMINES: SO-CALLED GUANIDINOTHIOUREAS AND THEIR ANHYDROACYL DERIVATIVES [PDF]

, 1960
S. N. DIXIT
openalex   +1 more source

Chiral Amplification and Regulation: Design and Applications of Circularly Polarized Luminescence‐Active Materials Derived From Macrocyclic Compounds

Aggregate, EarlyView.
The graphical abstract highlights the key concepts of this review, including chiral transfer and amplification mechanisms, macrocyclic compounds, circularly polarized luminescence (CPL) applications, chiral sensing, asymmetric catalysis, and stimuli‐responsive applications.
Wei Zhang, Mao‐Qin Liu, Yang Luo
wiley   +1 more source

A general copper catalytic system for cross-coupling of aryl iodides with chlorosilanes under reductive conditions. [PDF]

Chem Sci
Qiu L, Liu Y, Chen H, Song L, Xie W.
europepmc   +1 more source

Production Of 11C‐Labeled Amides Via “In‐Loop” 11C‐Carbonylation

Asian Journal of Organic Chemistry, EarlyView.
The current work utilizes carbon‐11 labelled aroyl dimethylaminopyridinium salts in a two‐step in‐loop carbonylative cross‐coupling reaction of aryl halides with [¹¹C]CO yielding a diverse range of carbon‐11 labelled primary benzamides with good to excellent yields.
Tanpreet Kaur, Xia Shao, Allen F. Brooks, Peter J. H. Scott   +3 more
wiley   +1 more source

Advances in transition-metal catalyzed C-H bond activation of amidines to synthesize aza-heterocycles. [PDF]

RSC Adv
Ren J, Xiong Y, Li Q, Wang B, Wang G, Wang B, Liu H, Yang X.   +7 more
europepmc   +1 more source

Ir‐Catalyzed Sulfur‐Directed Vinylic C─H Activation for the Stereoselective Synthesis of 1,3‐Dienes Using Alkynoates

Asian Journal of Organic Chemistry, EarlyView.
Ir‐catalyzed sulfur‐directed C─H alkenylation of alkynoates proceeded by using aryl methallyl sulfides. When DMAD was employed, 1,3‐dienes were initially formed and subsequently underwent thermal 1,5‐sigmatropic rearrangement to yield secondary products with high stereoselectivitiy.
Takanori Shibata, Haru Marumo
wiley   +1 more source

Copper catalyzed carbon-selenium bond formation via the coupling reaction of aryl halides, phenylboronic acid and Se. [PDF]

Sci Rep
Shirvandi Z, Ghorashi N, Rostami A.
europepmc   +1 more source

An Interaction between Kynurenine and the Aryl Hydrocarbon Receptor Can Generate Regulatory T Cells

Journal of Immunology, 2010
J. Mezrich, J. Fechner, Xiaoji Zhang, Brian P Johnson, W. Burlingham, C. Bradfield   +5 more
semanticscholar   +1 more source