Results 101 to 110 of about 12,716 (277)
Chiral Heptagon‐Embedded Double [6]Helicenes via Scholl Reaction
One bond makes the difference–two chiral and twisted polycyclic aromatic hydrocarbons (PAHs) show different emission behavior. The more flexible one (top) shows a double emission with one having a large anti‐Stokes shift. The two peaks are assigned to different conformers of one and the same compound.
Dan Wang +6 more
wiley +2 more sources
Tris(2,4,6-trifluorophenyl)borane: an efficient hydroboration catalyst [PDF]
The metal-free catalyst tris(2,4,6-trifluorophenyl)borane has demonstrated its extensive applications in the 1,2-hydroboration of numerous unsaturated reagents, namely alkynes, aldehydes and imines, consisting of a wide array of electron-withdrawing and ...
Lawson, James +2 more
core +2 more sources
Iron‐Mediated Electrochemical Cyclopropanation of Borodiiodomethane with Alkenes†
This work describes an electrochemical iron‐mediated cyclopropanation of borodiiodomethane with alkenes, resulting in the formation of boro‐substituted cyclopropanes. A key feature of this study is the unexpected discovery that the cathodically generated iron ion coordinates with a biquinoline ligand in situ, facilitating the electrochemical ...
Jie Li +3 more
wiley +1 more source
Atropselective syntheses of (-) and (+) rugulotrosin A utilizing point-to-axial chirality transfer [PDF]
Chiral, dimeric natural products containing complex structures and interesting biological properties have inspired chemists and biologists for decades.
A Zask +53 more
core +2 more sources
Pd‐Catalyzed C─C Bond Borylation of Biphenylenes Leading to Tri‐Ortho‐Substituted Biaryls
Palladium‐catalyzed ring‐opening C─C borylation of 1‐substituted biphenylenes yields a range of o,o,o′‐trisubstituted biaryls with two ortho‐boryl groups via selective cleavage of the least hindered C─C bond. The resulting diborylated products are readily amenable to sequential, site‐selective postfunctionalization.
Robyn V. Presland +5 more
wiley +1 more source
Iridium-catalysed regioselective borylation of carboranes via direct B–H activation
Functionalization of the multiple, similar, boron-hydrogen bonds in carboranes is difficult to achieve with selectivity. Here the authors report an iridium-catalysed borylation ofo-carboranes with high yields and regioselectivities.
Ruofei Cheng, Zaozao Qiu, Zuowei Xie
doaj +1 more source
Combining the Heck reaction with other transformations provides a powerful strategy to access diverse, complex compounds. Here, the authors report a weak coordination dominated Pd(0)-catalyzed quadruple C-H activation followed by hydro-functionalization,
Bo-Cheng Tang +7 more
doaj +1 more source
The formation of triplet Ni(II) complexes by activation of bromoalkenes with alkyl‐ or boryl Ni(I) is key to control the outcome of the reductive cross‐coupling of bromoalkanes precluding the formation of alkylboronates. We present a mechanistic study on the Ni‐catalyzed cross‐coupling reaction of bromoalkanes with diboron compounds as reductants.
Diego J. Cárdenas
wiley +1 more source
Trialkoxysilane-Induced Iridium-Catalyzed para-Selective C–H Bond Borylation of Arenes
An ideal approach for the construction of aryl boron compounds is to selectively replace a C–H bond in arenes with a C–B bond, and controlling regioselectivity is one of the most challenging aspects of these transformations.
Guodong Ju, Zhibin Huang, Yingsheng Zhao
doaj +1 more source
Ion Pairing-Driven Approach to Control Regioselectivity in Aromatic C(sp<sup>2</sup>)-H Borylation
Naoki Yasukawa
openalex +2 more sources

