Results 271 to 280 of about 538,570 (408)

meso‐Free Porphyrinoids

open access: yesAsian Journal of Organic Chemistry, EarlyView.
meso‐Free porphyrinoids are recognized as a versatile platform for further functionalization and oligomerization. The synthesis and characteristic features of such meso‐free porphyrinoids are reviewed. Abstract meso‐Unsubstituted (meso‐free) porphyrins have been an effective platform for creating versatile peripherally functionalized porphyrins and ...
Takayuki Tanaka   +2 more
wiley   +1 more source

Effect of Annulation Pattern on the Antiaromaticity of Thioether‐ and Sulfone‐Substituted Dinaphthopentalenes

open access: yesAsian Journal of Organic Chemistry, EarlyView.
Benzannulation of dibenzopentalene leads to dinaphthopentalenes, of which, we synthesized the linear and anti‐isomer as thioethers with various substituents. Depending on the annulation pattern, their optoelectronic properties strongly differ. Of particular interest, is an increased antiaromaticity resulting from the anti‐annulation pattern, indicated ...
Mathias Hermann   +2 more
wiley   +1 more source

Synthesis of a BINOL‐Derived Sulfide Catalyst Bearing a Diphenylmethanol Unit and Its Application in Asymmetric Bromolactonizations

open access: yesAsian Journal of Organic Chemistry, EarlyView.
The excellent catalytic performance of a BINOL‐derived sulfide catalyst bearing a diphenylmethanol unit was demonstrated in the highly enantioselective synthesis of γ‐butyrolactones via bromolactonization. Abstract A BINOL‐derived sulfide catalyst bearing a diphenylmethanol unit was prepared.
Yasuaki Furuya   +2 more
wiley   +1 more source

Producing aryl halides from lignin. [PDF]

open access: yesNat Commun
Liu Y   +9 more
europepmc   +1 more source

Interrupted Barton–Zard Reaction/Friedel–Crafts Alkylation Telescoped Reaction for the Synthesis of Pyrrolo[3,4‐b]indole Cores

open access: yesAsian Journal of Organic Chemistry, EarlyView.
An interrupted Barton–Zard reaction/Friedel–Crafts alkylation telescoped reaction provides aryl‐substituted pyrrolo[3,4‐b] cores in moderate‐to‐good yields as mostly single diastereomers. The reaction is tolerant of a wide range of electron‐deficient indoles and (hetero)aromatic nucleophiles, offering a modular approach for the synthesis of multi ...
Josip Rešetar   +5 more
wiley   +1 more source

Ni-Catalyzed Cyanation of (Hetero)Aryl Electrophiles Using the Nontoxic Cyanating Reagent K<sub>4</sub>[Fe(CN)<sub>6</sub>]. [PDF]

open access: yesACS Catal
Wilson NA   +7 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy